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ADAM MARTIN: All right.

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So in Monday's
lecture, we talked

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about how cells replicate, OK?

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And today, I want to talk about
how now an entire organ would

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essentially replicate.

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In this case, it's
not going to divide,

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but it's going to regenerate
or renew itself, OK?

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And so this involves adult
stem cells and also apoptosis ,

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which you've heard a little bit
about earlier in the course.

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And to explain this to you, I'm
going to have basically a model

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organ that we'll use.

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And we'll use it for
a couple lectures.

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And the model organ is going to
be the lining of the intestine,

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OK?

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So the lining of the intestine
is an epithelial tissue.

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And I'll tell you a
little bit about epithelia

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in just a minute.

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But you have the
intestinal epithelium.

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And this is the-- these
are the cells that

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are the lining of
the intestine, OK?

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And one of the reasons that
I've chosen this system

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is because the lining
of your intestine

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has pretty remarkable
regenerative capabilities, OK?

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So your small intestine renews
about every four to five days,

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OK?

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So the vast majority of
your cells in the intestine

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were basically derived in the
last four to five days, OK?

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So humans aren't as
cool as some organisms,

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like newts, in that you
can't cut off your arm

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and have it grow back.

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But at least we
have the intestine,

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which undergoes a pretty
dramatic regeneration, OK?

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And this is not--

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the intestine is unique
in how rapid this is.

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But you have other tissues that
also exhibit continual renewal,

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like your skin and
your blood cells.

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And even the cells
of your that line

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your insides of your lungs,
they do exhibit renewal

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capabilities, OK?

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And so I'm going to use the
intestine as a model system.

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It doesn't mean it doesn't
happen in other tissues.

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But it just happens
that we can--

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we really understand
the intestine system

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maybe a little bit more
than many other systems.

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So I'm going to use
it as an example.

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So in thinking about the
lining of your intestine,

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it's important, and it
has important functions.

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One important function
of this lining

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is it has to absorb
nutrients from food going

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through your intestine, OK?

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So it exhibits a nutrient
absorption function.

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Now, the lining of your intimate
intestine, much like your skin,

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is also a barrier between
the inside of your body

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and the outside world, right?

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Because basically, the
inside of your intestine

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is contiguous with the
outside world, right?

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If you open your
mouth, you can get down

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to the inside of
your intestine, OK?

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So it serves also an
important barrier function.

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And one point I want to make
about this system right now

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is that the intestinal
epithelium, like many

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of your other organs, are
composed of multiple cell

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types, OK?

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So it also has
multiple cell types.

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OK.

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So let's now consider the
lining of the intestine.

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And the way the intestine
morphologically looks

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is that there are a
series of invaginations.

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So this is a cross-section
view through the intestine.

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So you have to imagine that
this is a cross-section view,

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but that this is a plane.

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And it's a plane with a lot
of invaginations in the plane,

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but also protrusions
out of the plane.

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And so you have to remember--

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you have to think of
this as a surface.

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And then it's wrapped
up into a tube, OK?

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So this is just a very
simple cross-section image

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of the intestine, OK?

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And the lining of the
intestine is a sheet of cells.

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So this lining is composed
of many, many cells.

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They're columnar in morphology.

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So what I've drawn here
is just a small section

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of the intestine.

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This would be the
lumen, out here.

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This is where the
food is, or the food

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going through your
intestine would be.

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And then below here, this
is interstitial fluid inside

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of your body basically,
interstitial, OK?

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So the food's up here.

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The rest of your
body is down here.

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And you can see
that there are there

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there's a structure to it.

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It's not just a flat
surface that's wrapped up,

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but there are invaginations.

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And the invaginations are known
as intestinal crypts, right?

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Much like you would--

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if you bury something, like a
body, it would go below ground.

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So the crypt is below
the surface of the lumen.

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And this these projections,
out here, are known as villi.

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So they're the villi
of your gut, OK?

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Now, if we consider--

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and this lining is made
up of multiple cell

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types, which I've
outlined up here

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and which are in your handout.

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So you don't have
to write these down.

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But this is just
making the point

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that there are various
differentiated cell types.

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There are enterocytes, which
are the absorptive cells.

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These are the cells that
are taking in nutrients

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and transporting
them into your body.

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There are enteroendocrine
cells that

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play an important signaling
function in the gut to regulate

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the biology of the gut system.

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There are a goblet cells,
which secrete mucus

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into the intestine system, which
protects these epithelial cells

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from digestive enzymes that
are present in the lumen.

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And there is this last
cell type, the paneth cell,

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which functions as an important
role in regulating stem cells,

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as I'll outline
in just a minute.

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So these are all the
differentiated cell types.

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But there's a type
of cell that's

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an undifferentiated cell type.

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And that's the
intestinal stem cell,

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which will be the hero
of today's lecture.

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All right.

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Now, if we consider just
a small group of cells,

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what these cells look
like is this, OK?

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So these are what are
known as epithelial cells.

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And epithelial cells
have certain properties.

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The first is you see that this
end of the epithelial cell

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looks different
from this end, OK?

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And this is called an
apical-basal polarity.

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So much like neurons
have a polarity where

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the on one side of the
neuron there are dendrites

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and on the other side of
the neuron there's an axon,

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these cells have another
type of polarity, which is

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called apical-basal polarity.

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So the side facing
the lumen is apical.

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So the lumen would be up here.

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And the basal side
would be down here, OK?

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So this is basically oriented
along this axis of the tissue,

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OK?

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where apical is on this side,
basal is on this side, OK?

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And these projections from
the individual cell, these

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are called microvilli.

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And essentially,
these plasma membrane

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corrugations increase
the surface area

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through which nutrients can be
absorbed into these cells, OK?

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Now, one other defining
feature of these cells

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is they have proteins that
protrude from the plasma

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membrane.

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And these are adhesion proteins
that couple the cells together.

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And actually, the cells
are stuck together

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much tighter than I'm
drawing here, such

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that the cells form a
barrier so that things

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can pass unregulated from
the lumen into the body, OK?

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But these proteins,
which I'm drawing

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sticking out of the
membranes of the cells,

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are adhesion proteins.

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And these adhesion
proteins simply

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link the cells together
such that they form

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a sheet of cells or tissue.

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So they link cells together, OK?

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So these are two of the key
properties of epithelia.

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They have an
apical-basal polarity.

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And they also exhibit
cell-to-cell adhesion,

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such as the cells reach out
and connect to each other.

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And they basically are glued
together, or Velcroed together

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such that they don't
easily come apart.

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OK.

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Now, in considering this
system, what I'm going to tell

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you is that there is
renewal of this lining.

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And the renewal starts at
the base of the crypts, OK?

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So there's going to be renewal.

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And this cell renewal is at
the base of the crypts, right?

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There are many of
these crypts, right?

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You have you have
like the surface,

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but there are many,
many invaginations

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that are present in your gut.

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And the renewal is happening at
the base of these crypts, OK?

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And that's because at
the base of these crypts

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are where a type of cell, known
as intestinal stem cells, lie,

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OK?

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So it's at the base
of these crypts

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where there are what are known
as intestinal stem cells.

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And I'm going to abbreviate
these ISCs for this,

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so I don't have to write
out intestinal stem cell

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whenever I tell
you about them, OK?

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Now, that's where
renewal occurs.

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And if you just had more
and more cells getting

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put in the system without
any removal of cells,

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then the organ would get
bigger and bigger, right?

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And so our intestine
more or less

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staying the same size at
this point in our life.

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And so in addition to renewal,
there's also cell death.

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And what happens when
cell death occurs

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is that cells are shed
from the intestinal lining

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into the lumen.

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So cells are shed
into the lumen.

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And then they just go with
the rest of the crap that's

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in your intestinal lumen.

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And it's eventually
removed from the body, OK?

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So some cells are leaving the
tissue and going into the lumen

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after they've existed for a
few days in the intestine, OK?

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So to have an organ
then the constant size

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renewal has to essentially be
more or less equal to death,

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OK?

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And so you can think of this
as a type of homeostatic state

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for this tissue where, if
renewal equals death, you have

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what is known as tissue
homeostasis, where

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the number of cells in
the system as a whole

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is basically remaining the same,
even though there's constantly

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new cells going
into this system.

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But then the cells are also--

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the older cells are being
removed from the system.

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So what's really
key in this process

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are these intestinal stem cells.

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So I'm first going to
tell you about stem cells.

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And these are what I would
define as adult stem cells, OK?

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So they're stem cells
that are associated

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with a particular organ, OK?

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And I want to
differentiate this right

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now between these
types of stem cells

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and another type of
stem cell that we're

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going to talk about later
in the course, which

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is an embryonic stem cell.

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So adult stem cells--

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these stem cells, like
intestinal stem cells,

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are associated with
a specific organ.

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And they only give
rise to cell types that

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are present in that organ, OK?

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So they're not-- they can't give
rise to any type of cell type.

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Your adult stem cells are really
specific-- organ-specific,

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we'll say.

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In contrast, embryonic
stem cells are--

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these stem cells have
more possibilities.

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They can give rise to
pretty much any cell

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type in an entire organism, OK?

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So you can think of
these adult stem cells

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as being more restricted
in their fates

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than the embryonic stem cells.

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And so what adult
stem cells are called

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is they're called multipotent,
because they can give rise

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to multiple
different cell types,

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but not all of the
cell types that are

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present in an organism, right?

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An intestinal stem cell
will not be giving rise

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00:15:36,570 --> 00:15:42,490
to a blood cell or other cell
types in other organs, right?

249
00:15:42,490 --> 00:15:44,880
It's restricted to
just giving rise

250
00:15:44,880 --> 00:15:47,910
to cells that are
present in that organ.

251
00:15:47,910 --> 00:15:50,460
In contrast,
embryonic stem cells

252
00:15:50,460 --> 00:15:56,280
are what are known as
totipotent, or sometimes

253
00:15:56,280 --> 00:16:00,810
pluripotent, where
this type of cell

254
00:16:00,810 --> 00:16:04,440
really is capable of making
any type of cell that

255
00:16:04,440 --> 00:16:08,370
is present in an
adult organism, OK?

256
00:16:08,370 --> 00:16:11,400
So that's less restricted
than the adult stem cells.

257
00:16:11,400 --> 00:16:14,100
And we're going to come back
to these embryonic stem cells

258
00:16:14,100 --> 00:16:16,270
towards the end of the course.

259
00:16:16,270 --> 00:16:19,710
But for understanding
cancer and also

260
00:16:19,710 --> 00:16:22,320
tissue homeostasis
in the intestine,

261
00:16:22,320 --> 00:16:24,930
we're really needing to focus
on the adult stem cells.

262
00:16:28,300 --> 00:16:28,800
OK.

263
00:16:28,800 --> 00:16:32,620
So these adult stem cells
have two key properties.

264
00:16:32,620 --> 00:16:34,710
The first is what I just said.

265
00:16:34,710 --> 00:16:35,850
They're multipotent.

266
00:16:41,500 --> 00:16:43,830
And what multipotent
means is that they

267
00:16:43,830 --> 00:16:48,510
can give rise to multiple
different cell types.

268
00:16:48,510 --> 00:16:54,645
So this stem cell gives
rise to multiple cell types.

269
00:17:00,270 --> 00:17:03,420
And this is associated usually
with a single organ system.

270
00:17:10,619 --> 00:17:11,119
OK.

271
00:17:11,119 --> 00:17:14,760
So in the case of the
intestinal stem cell,

272
00:17:14,760 --> 00:17:18,119
the intestinal stem
cell is multipotent.

273
00:17:18,119 --> 00:17:20,490
And it can give rise to
many different terminally

274
00:17:20,490 --> 00:17:22,480
differentiated cells.

275
00:17:22,480 --> 00:17:25,890
And you can see here I've just
written in example cell types

276
00:17:25,890 --> 00:17:28,349
that the intestinal
cell could generate.

277
00:17:28,349 --> 00:17:31,140
It can generate any of the
four different types of cells

278
00:17:31,140 --> 00:17:35,850
that I introduced to you at
the beginning of the lecture.

279
00:17:35,850 --> 00:17:38,850
The other key aspect
of this system

280
00:17:38,850 --> 00:17:41,010
is that, in addition
to generating

281
00:17:41,010 --> 00:17:43,740
all of these
different cell types,

282
00:17:43,740 --> 00:17:47,610
the stem cell can
also renew itself, OK?

283
00:17:47,610 --> 00:17:51,810
So the other key property
is this self-renewal.

284
00:17:56,230 --> 00:18:05,280
So the intestinal stem
cell also gives rise

285
00:18:05,280 --> 00:18:10,200
to another intestinal stem cell.

286
00:18:10,200 --> 00:18:13,260
So it basically
duplicates itself such

287
00:18:13,260 --> 00:18:16,620
that you still have a
stem cell in the organ.

288
00:18:16,620 --> 00:18:19,830
And then one of
the daughter cells

289
00:18:19,830 --> 00:18:23,080
is self-renewed and
remains a stem cell.

290
00:18:23,080 --> 00:18:26,640
The other daughter cell
can go on to divide

291
00:18:26,640 --> 00:18:30,780
further and give rise to these
differentiated cell types, OK?

292
00:18:39,000 --> 00:18:39,500
All right.

293
00:18:39,500 --> 00:18:41,660
So one question
you might be asking

294
00:18:41,660 --> 00:18:45,860
yourself is, how is it that--

295
00:18:45,860 --> 00:18:49,160
what regulates
whether or not a cell

296
00:18:49,160 --> 00:18:52,370
will go on to
differentiate or whether it

297
00:18:52,370 --> 00:18:56,780
will stay a stem cell?

298
00:18:56,780 --> 00:18:59,300
And the answer to
this question involves

299
00:18:59,300 --> 00:19:01,520
communication between
this stem cell

300
00:19:01,520 --> 00:19:05,480
and other cells in the system.

301
00:19:05,480 --> 00:19:09,110
And it involves a
special type of cell

302
00:19:09,110 --> 00:19:11,810
called a stem cell niche cell.

303
00:19:11,810 --> 00:19:14,900
And so I'm going to tell
you about a model, which

304
00:19:14,900 --> 00:19:17,210
is the stem cell niche model.

305
00:19:17,210 --> 00:19:19,445
And what the stem
cell niche model is,

306
00:19:19,445 --> 00:19:23,870
is that basically there is
a niche or compartment which

307
00:19:23,870 --> 00:19:28,490
promotes the self-renewal of
cells in that compartment that

308
00:19:28,490 --> 00:19:30,300
makes them stem cells.

309
00:19:30,300 --> 00:19:36,890
So the stem cell niche you can
think of as a compartment where

310
00:19:36,890 --> 00:19:43,070
signals, similar to the types of
signals that we've been talking

311
00:19:43,070 --> 00:19:46,220
about over the past
four or five lectures,

312
00:19:46,220 --> 00:19:49,940
regulate the behavior of the
cell to ensure self-renewal

313
00:19:49,940 --> 00:19:53,420
and to suppress differentiation,
so a compartment

314
00:19:53,420 --> 00:19:58,625
where signals promote
stem cell renewal.

315
00:20:09,550 --> 00:20:13,360
I want to ask you one question
before I move on, which

316
00:20:13,360 --> 00:20:15,970
is, how would you define--

317
00:20:15,970 --> 00:20:17,980
how would you
determine that there

318
00:20:17,980 --> 00:20:20,860
is a special type of cell
that gives rise to all

319
00:20:20,860 --> 00:20:24,280
of the cells in an organ?

320
00:20:24,280 --> 00:20:29,740
If you were tasked with
finding this and determining

321
00:20:29,740 --> 00:20:32,650
whether this was true or
not, how might you do it?

322
00:20:32,650 --> 00:20:35,980
Does anyone have an idea of
what experiment they would do,

323
00:20:35,980 --> 00:20:40,300
or what criteria they would
have to determine whether or not

324
00:20:40,300 --> 00:20:41,140
this is a case?

325
00:20:49,990 --> 00:20:53,140
Let's say I gave
you a cell, right?

326
00:20:53,140 --> 00:20:54,910
In a dish.

327
00:20:54,910 --> 00:20:57,850
And I asked you to
tell me whether or not

328
00:20:57,850 --> 00:21:01,450
you would think this
is a stem cell or not.

329
00:21:01,450 --> 00:21:03,795
Yes, miles?

330
00:21:03,795 --> 00:21:09,500
AUDIENCE: [INAUDIBLE]

331
00:21:09,500 --> 00:21:10,586
ADAM MARTIN: Mm-hmm.

332
00:21:10,586 --> 00:21:13,051
AUDIENCE: One cell is
produced by the same cell,

333
00:21:13,051 --> 00:21:16,995
assuming that it's
not a stem cell

334
00:21:16,995 --> 00:21:25,637
but if the cell [INAUDIBLE]
it's a stem cell.

335
00:21:25,637 --> 00:21:26,470
ADAM MARTIN: Mm-hmm.

336
00:21:26,470 --> 00:21:30,580
So Miles suggested he would like
to take the cell that I just

337
00:21:30,580 --> 00:21:34,780
gifted him, and let it grow up,
and determine whether it gives

338
00:21:34,780 --> 00:21:37,000
rise to multiple cell types.

339
00:21:37,000 --> 00:21:39,370
And Miles said that,
if it just gave rise

340
00:21:39,370 --> 00:21:41,500
to a single cell type,
that would suggest

341
00:21:41,500 --> 00:21:43,310
that it's not a stem cell.

342
00:21:43,310 --> 00:21:46,690
But if it gave rise to
multiple cell types,

343
00:21:46,690 --> 00:21:49,450
then it could be
a stem cell, OK?

344
00:21:49,450 --> 00:21:53,110
And it's this type
of experiment that--

345
00:21:53,110 --> 00:21:55,480
this type of experiment
has been done,

346
00:21:55,480 --> 00:22:00,160
where you can take an
intestine from mice,

347
00:22:00,160 --> 00:22:02,770
and even you can take
tissue from humans,

348
00:22:02,770 --> 00:22:05,480
and you can associate
the cells from each other

349
00:22:05,480 --> 00:22:09,520
so that you're left with
single cells that are separate.

350
00:22:09,520 --> 00:22:13,030
And you can then use some
type of flow cytometry

351
00:22:13,030 --> 00:22:14,710
to separate cells.

352
00:22:14,710 --> 00:22:16,900
And you might be
interested in a cell that

353
00:22:16,900 --> 00:22:20,260
maybe expresses some marker
that you're interested in.

354
00:22:20,260 --> 00:22:23,710
And you can separate those
cells and isolate them.

355
00:22:23,710 --> 00:22:26,530
And then you can take
an individual cell

356
00:22:26,530 --> 00:22:29,200
and grow it in a dish, OK?

357
00:22:29,200 --> 00:22:32,840
And this has been done
for intestinal stem cells.

358
00:22:32,840 --> 00:22:35,590
And if you take an
intestinal stem cell

359
00:22:35,590 --> 00:22:38,140
and you grow it in a
dish, it can grow up

360
00:22:38,140 --> 00:22:40,780
and form a bulk of tissue.

361
00:22:40,780 --> 00:22:44,650
But what's really
remarkable about the result

362
00:22:44,650 --> 00:22:48,100
of this experiment is
that, from a stem cell,

363
00:22:48,100 --> 00:22:50,290
you get this massive tissue.

364
00:22:50,290 --> 00:22:53,380
But it self--organizes into
a structure that very much

365
00:22:53,380 --> 00:22:59,150
resembles a normal gut, meaning
that there are crypts where

366
00:22:59,150 --> 00:23:01,740
the stem cells are localized.

367
00:23:01,740 --> 00:23:03,490
And then if you look
at the different cell

368
00:23:03,490 --> 00:23:06,580
types in this, what's
known as an organoid,

369
00:23:06,580 --> 00:23:10,570
you see all of the different
cell types that are normally

370
00:23:10,570 --> 00:23:12,850
present in the gut, OK?

371
00:23:12,850 --> 00:23:16,090
And so this is an example
of a type of experiment

372
00:23:16,090 --> 00:23:19,150
that's done to
show whether or not

373
00:23:19,150 --> 00:23:22,780
a certain cell has the
capability of functioning

374
00:23:22,780 --> 00:23:24,190
like a stem cell, OK?

375
00:23:24,190 --> 00:23:26,080
So if you start
with a stem cell,

376
00:23:26,080 --> 00:23:30,820
you can regenerate the entire
organ system essentially.

377
00:23:30,820 --> 00:23:34,360
You might also be familiar
with bone marrow transplants.

378
00:23:34,360 --> 00:23:39,760
And so if you kill all the
hematopoietic stem cells

379
00:23:39,760 --> 00:23:42,460
in, let's say, a
mouse, then you can

380
00:23:42,460 --> 00:23:45,700
transplant in a single
hematopoietic stem cell

381
00:23:45,700 --> 00:23:46,870
into that system.

382
00:23:46,870 --> 00:23:52,990
And it will regenerate all the
blood cells in that system, OK?

383
00:23:52,990 --> 00:23:57,010
So those are just a few examples
of how one might functionally

384
00:23:57,010 --> 00:23:59,860
define a stem cell in
an experimental setting.

385
00:24:02,480 --> 00:24:02,980
All right.

386
00:24:02,980 --> 00:24:06,190
So now, I want to tell you
about the types of signals

387
00:24:06,190 --> 00:24:09,960
and how these signals are
promoting stem cell renewal,

388
00:24:09,960 --> 00:24:10,630
OK?

389
00:24:10,630 --> 00:24:13,720
So in this case, the
niche, stem cell niche

390
00:24:13,720 --> 00:24:14,920
is going to be right here.

391
00:24:17,910 --> 00:24:20,020
And the types of
signals involved--

392
00:24:20,020 --> 00:24:23,440
I'll just draw some cells here.

393
00:24:23,440 --> 00:24:26,230
One of the types of
cells that's part

394
00:24:26,230 --> 00:24:29,440
of the niche in the
intestine is the cell type

395
00:24:29,440 --> 00:24:31,705
that I introduced you
as the paneth cell.

396
00:24:34,360 --> 00:24:38,230
And these paneth cells localized
to the base of the crypts

397
00:24:38,230 --> 00:24:41,230
together with the
intestinal stem cells.

398
00:24:41,230 --> 00:24:44,950
And what paneth cells
do is they send a signal

399
00:24:44,950 --> 00:24:46,960
to neighboring cells.

400
00:24:46,960 --> 00:24:49,420
And this signal is a Wnt
signal, which I'll tell you

401
00:24:49,420 --> 00:24:51,050
about in just a minute.

402
00:24:51,050 --> 00:24:54,100
And so this is the
intestinal stem cell here.

403
00:24:54,100 --> 00:24:58,660
And the paneth cell is signaling
to that intestinal stem cell

404
00:24:58,660 --> 00:25:02,950
through a secreted
ligand known as Wnt.

405
00:25:02,950 --> 00:25:04,870
So Wnt is a secreted ligand.

406
00:25:08,600 --> 00:25:17,300
And this signal is what's known
as a juxtacrine signal, which

407
00:25:17,300 --> 00:25:19,940
just means that the cells
have to be adjacent,

408
00:25:19,940 --> 00:25:25,430
or juxtaposed, to each other
in order for the sending cell

409
00:25:25,430 --> 00:25:28,130
to signal to its neighbor, OK?

410
00:25:28,130 --> 00:25:29,990
So it's not
signaling long range,

411
00:25:29,990 --> 00:25:33,620
but it's signaling to
a neighboring cell, OK?

412
00:25:33,620 --> 00:25:36,770
So now, if we think about
this intestinal stem cell,

413
00:25:36,770 --> 00:25:41,600
one thing intestinal stem
cells do as they divide, right?

414
00:25:41,600 --> 00:25:44,990
So this intestinal
stem cell could divide.

415
00:25:44,990 --> 00:25:47,300
Here is a cell in mitosis.

416
00:25:47,300 --> 00:25:50,210
It rounds up and divides.

417
00:25:50,210 --> 00:25:51,920
Here, you still have
your paneth cell.

418
00:25:56,950 --> 00:25:58,960
And then when this
cell divides, then it's

419
00:25:58,960 --> 00:26:02,200
going to be two cells, OK?

420
00:26:02,200 --> 00:26:06,940
So now, paneth
cell, another cell.

421
00:26:06,940 --> 00:26:08,780
Here the two daughter cells.

422
00:26:08,780 --> 00:26:11,170
Here's the paneth cell.

423
00:26:11,170 --> 00:26:14,800
The paneth cell is still
secreting this Wnt signal.

424
00:26:14,800 --> 00:26:17,110
So you have Wnt
getting secreted.

425
00:26:17,110 --> 00:26:19,330
And it's going to
signal to its neighbor.

426
00:26:19,330 --> 00:26:21,940
But this cell is starting
to get farther and farther

427
00:26:21,940 --> 00:26:24,070
away from that signal, right?

428
00:26:24,070 --> 00:26:26,680
So you can imagine this
is happening right here

429
00:26:26,680 --> 00:26:28,840
in the tissue,
where this cell is

430
00:26:28,840 --> 00:26:31,990
at the boundary
of the niche, OK?

431
00:26:31,990 --> 00:26:34,720
So this cell that gets
pushed out of the niche

432
00:26:34,720 --> 00:26:44,140
is going to start to
differentiate, OK?

433
00:26:44,140 --> 00:26:48,130
Because it's no longer
seeing the signal, OK?

434
00:26:48,130 --> 00:26:50,710
So it's the lack
of the Wnt signal

435
00:26:50,710 --> 00:26:53,530
which tells cells
basically that they

436
00:26:53,530 --> 00:26:56,620
should start differentiating
into the various cell

437
00:26:56,620 --> 00:26:58,160
types of the gut.

438
00:26:58,160 --> 00:27:00,880
But the cells that are stuck
at the base of the crypt,

439
00:27:00,880 --> 00:27:05,360
down with the paneth cells, are
still getting the Wnt signal.

440
00:27:05,360 --> 00:27:12,730
And so they remain an
intestinal stem cell, OK?

441
00:27:12,730 --> 00:27:15,910
So here is just a diagram
showing you part of that.

442
00:27:15,910 --> 00:27:19,150
So the niche is down here,
where you have the stem cells.

443
00:27:19,150 --> 00:27:21,760
The paneth cells would be
some of these blue cells

444
00:27:21,760 --> 00:27:22,720
at the base.

445
00:27:22,720 --> 00:27:27,100
But there are also other cells
below the epithelial lining

446
00:27:27,100 --> 00:27:31,630
known as stromal cells that
are also secreting Wnt.

447
00:27:31,630 --> 00:27:34,210
And so this
compartment down here

448
00:27:34,210 --> 00:27:37,720
has high Wnt ligan activity.

449
00:27:37,720 --> 00:27:42,130
And that tells cells that
remain here to stay stem cells.

450
00:27:42,130 --> 00:27:43,960
But the cells that
are getting pushed up

451
00:27:43,960 --> 00:27:47,170
and moving up towards
the lumen, they no longer

452
00:27:47,170 --> 00:27:48,680
receive this signal.

453
00:27:48,680 --> 00:27:52,300
And so they are going to
start to differentiate, OK?

454
00:27:52,300 --> 00:27:56,320
So you can think of this
system as almost a conveyor

455
00:27:56,320 --> 00:27:59,320
belt. There's a conveyor
belt-like movement of cells

456
00:27:59,320 --> 00:28:02,610
from the base of the crypt up
towards the tip of the villis,

457
00:28:02,610 --> 00:28:03,310
OK?

458
00:28:03,310 --> 00:28:06,610
And when the cells move
away from the niche cells,

459
00:28:06,610 --> 00:28:09,940
then they no longer have
the self-renewal signal.

460
00:28:09,940 --> 00:28:12,130
And therefore, they go
on to differentiate.

461
00:28:18,560 --> 00:28:19,060
OK.

462
00:28:19,060 --> 00:28:20,510
We'll go back for now.

463
00:28:20,510 --> 00:28:21,010
All right.

464
00:28:21,010 --> 00:28:25,150
Now, I want to tell you a little
bit about this signal, Wnt,

465
00:28:25,150 --> 00:28:28,990
because it's something that's
come up before in the lecture,

466
00:28:28,990 --> 00:28:30,830
even though you
might not know it.

467
00:28:30,830 --> 00:28:34,270
So Wnt is a ligand.

468
00:28:34,270 --> 00:28:37,180
So it functions much
like a growth factor.

469
00:28:37,180 --> 00:28:40,540
This is a protein that is
secreted from the cell,

470
00:28:40,540 --> 00:28:43,630
and then binds to
receptors on other cells,

471
00:28:43,630 --> 00:28:48,010
and induces signaling
events in those cells, OK?

472
00:28:48,010 --> 00:28:49,780
And Wnt stands for--

473
00:28:49,780 --> 00:28:54,910
the W stands for wingless, OK?

474
00:28:54,910 --> 00:28:58,120
So you remember from
earlier in the semester,

475
00:28:58,120 --> 00:29:04,180
wingless was
identified as a mutant

476
00:29:04,180 --> 00:29:09,220
that disrupts the formation
of wings in the fly, OK?

477
00:29:09,220 --> 00:29:14,920
So one of the places where
these genes were discovered

478
00:29:14,920 --> 00:29:16,330
is in the fly.

479
00:29:16,330 --> 00:29:23,230
The nt of Wnt comes
from int 1, which

480
00:29:23,230 --> 00:29:28,540
stands for the integration
of mouse mammary virus 1.

481
00:29:28,540 --> 00:29:31,000
Sorry, that's a little
bit more of a mouthful.

482
00:29:31,000 --> 00:29:34,015
The integration of mouse--

483
00:29:36,850 --> 00:29:43,460
actually, sorry, mouse
mammary tumor virus 1.

484
00:29:43,460 --> 00:29:44,920
I forgot the tumor part of it.

485
00:29:52,590 --> 00:29:53,500
OK.

486
00:29:53,500 --> 00:29:56,740
So the W in Wnt
is from wingless.

487
00:29:56,740 --> 00:30:01,060
The nt in Wnt is from int 1, OK?

488
00:30:01,060 --> 00:30:06,190
And so as you can see, there
are two different systems

489
00:30:06,190 --> 00:30:09,210
where this type of
gene was discovered.

490
00:30:09,210 --> 00:30:11,840
They are very disparate
from each other.

491
00:30:11,840 --> 00:30:16,090
One was in a developmental
mutant, in the fruit fly.

492
00:30:16,090 --> 00:30:21,070
The other was in a
mouse system, where

493
00:30:21,070 --> 00:30:24,070
the integration of the
virus caused over-expression

494
00:30:24,070 --> 00:30:28,420
of Wnt, which caused it
as tumor genesis, OK?

495
00:30:28,420 --> 00:30:32,200
So these disparate systems
led to the identification

496
00:30:32,200 --> 00:30:35,350
of this Wnt molecule.

497
00:30:35,350 --> 00:30:39,310
And this is a defining
member of a signaling pathway

498
00:30:39,310 --> 00:30:42,170
that regulates
stem cell renewal.

499
00:30:42,170 --> 00:30:44,800
And I just want to briefly
go through the logic

500
00:30:44,800 --> 00:30:47,980
of the signaling
pathway, because I want

501
00:30:47,980 --> 00:30:50,860
you to get a sense that not
all signaling pathways are

502
00:30:50,860 --> 00:30:52,840
like Ras-MAP kinase,
but there can be

503
00:30:52,840 --> 00:30:55,450
different regulatory logic, OK?

504
00:30:55,450 --> 00:30:59,380
So what's the regulatory
logic of this pathway?

505
00:31:03,080 --> 00:31:11,270
So the regulatory logic
is shown in this cartoon.

506
00:31:11,270 --> 00:31:13,570
And I'm going to
start with a cell that

507
00:31:13,570 --> 00:31:15,970
does not see Wnt ligand.

508
00:31:15,970 --> 00:31:19,270
So that would be the
case on the left here.

509
00:31:19,270 --> 00:31:20,980
So if there's no Wnt ligand--

510
00:31:20,980 --> 00:31:24,110
I want you to focus on
what's going on here--

511
00:31:24,110 --> 00:31:28,420
there's a complex that's present
in the cytoplasm of the cell.

512
00:31:28,420 --> 00:31:30,310
And what it's doing
is it's destroying

513
00:31:30,310 --> 00:31:33,700
this beta-catenin protein, OK?

514
00:31:33,700 --> 00:31:36,880
So what beta-catenin is--

515
00:31:36,880 --> 00:31:41,590
among other things, it's a
transcriptional coactivator.

516
00:31:41,590 --> 00:31:43,345
So it's basically a
transcription factor.

517
00:31:48,580 --> 00:31:52,780
So it works with another protein
to regulate the expression

518
00:31:52,780 --> 00:31:56,720
of certain genes, OK?

519
00:31:56,720 --> 00:32:01,180
And in the absence of Wnt,
this beta-catenin transcription

520
00:32:01,180 --> 00:32:07,090
factor is destroyed and is not
able to get into the nucleus,

521
00:32:07,090 --> 00:32:09,460
OK?

522
00:32:09,460 --> 00:32:19,000
So if there's no Wnt, then
beta-catenin is destroyed.

523
00:32:22,390 --> 00:32:24,310
And it's destroyed
using a system

524
00:32:24,310 --> 00:32:26,770
that I introduced in
Monday's lecture, which

525
00:32:26,770 --> 00:32:31,030
is regulated proteolysis
by polyubiquitination, OK?

526
00:32:31,030 --> 00:32:32,390
So the first real--

527
00:32:35,050 --> 00:32:42,010
so you have
regulated proteolysis

528
00:32:42,010 --> 00:32:43,790
by polyubiquitination.

529
00:32:47,200 --> 00:32:50,500
So the way this
works, as seen here,

530
00:32:50,500 --> 00:32:56,620
is that beta-catenin is
bound by this complex.

531
00:32:56,620 --> 00:33:00,250
And there's a kinase that
phosphorylates beta-catenin.

532
00:33:00,250 --> 00:33:02,680
And then the
phosphorylated beta-catenin

533
00:33:02,680 --> 00:33:05,410
recruits this E3
ubiquitin ligase, which

534
00:33:05,410 --> 00:33:08,320
polyubiquitinates it, OK?

535
00:33:08,320 --> 00:33:10,670
So that leads to the
destruction of beta-catenin

536
00:33:10,670 --> 00:33:14,230
in the absence of a Wnt signal.

537
00:33:14,230 --> 00:33:17,020
But when Wnt ligand
is around, this

538
00:33:17,020 --> 00:33:20,980
leads to the disassembly of
this complex, which is known

539
00:33:20,980 --> 00:33:23,110
as the destruction complex.

540
00:33:23,110 --> 00:33:26,410
And that leads to
beta-catenin accumulating.

541
00:33:26,410 --> 00:33:29,230
And once it accumulates,
it goes into the nucleus

542
00:33:29,230 --> 00:33:32,710
and starts changing
gene expression, OK?

543
00:33:32,710 --> 00:33:45,720
So in the presence of Wnt,
beta-catenin is nuclear.

544
00:33:45,720 --> 00:33:48,640
And that's where it needs to
be, if it's going to regulate

545
00:33:48,640 --> 00:33:51,550
gene expression, OK?

546
00:33:51,550 --> 00:33:54,580
So what you see is the
logic of this pathway

547
00:33:54,580 --> 00:33:57,880
is you have a double
negative, where

548
00:33:57,880 --> 00:34:03,125
you have a complex, which
is known as the destruction

549
00:34:03,125 --> 00:34:03,625
complex.

550
00:34:08,219 --> 00:34:10,780
And it includes this
gene, APC, which we're

551
00:34:10,780 --> 00:34:12,790
going to talk about on Friday.

552
00:34:12,790 --> 00:34:15,909
This destruction complex
is inhibiting beta-catenin

553
00:34:15,909 --> 00:34:16,960
by destroying it.

554
00:34:21,420 --> 00:34:26,860
And the way that Wnt induces
beta-catenin activation

555
00:34:26,860 --> 00:34:29,830
is by inhibiting the inhibitor.

556
00:34:29,830 --> 00:34:33,889
So Wnt inhibits the
destruction complex,

557
00:34:33,889 --> 00:34:37,150
which then stabilizes
beta-catenin and allows

558
00:34:37,150 --> 00:34:39,489
it to go to the nucleus, OK?

559
00:34:39,489 --> 00:34:42,280
So the other piece
of the logic here

560
00:34:42,280 --> 00:34:48,520
is you have inhibition
of an inhibitor

561
00:34:48,520 --> 00:34:50,487
to activate beta-catenin.

562
00:34:55,469 --> 00:34:57,385
Any questions on the pathway?

563
00:35:04,210 --> 00:35:04,710
OK.

564
00:35:04,710 --> 00:35:11,040
So now that we have our
intestinal stem cells

565
00:35:11,040 --> 00:35:16,710
and we have a way, by increasing
Wnt in this compartment,

566
00:35:16,710 --> 00:35:22,500
to maintain the intestinal stem
cells through self-renewal, now

567
00:35:22,500 --> 00:35:25,080
we have to talk about
the compensatory

568
00:35:25,080 --> 00:35:28,260
mechanism of death,
which allows this tissue

569
00:35:28,260 --> 00:35:29,670
to maintain homeostasis.

570
00:35:34,930 --> 00:35:35,430
OK.

571
00:35:35,430 --> 00:35:39,870
So death-- in this case,
death is going to be useful.

572
00:35:39,870 --> 00:35:45,430
And the process of death
is called apoptosis.

573
00:35:48,710 --> 00:35:51,600
And apoptosis is
Greek for falling off.

574
00:36:01,430 --> 00:36:03,510
And that's essentially
what these cells

575
00:36:03,510 --> 00:36:07,920
are doing, because
the cells, as they

576
00:36:07,920 --> 00:36:11,280
move from the base of the
crypt up towards the lumen--

577
00:36:11,280 --> 00:36:12,870
eventually, they're
going to fall off

578
00:36:12,870 --> 00:36:16,630
into the lumen of the intestine.

579
00:36:16,630 --> 00:36:19,190
So again, I'll draw.

580
00:36:19,190 --> 00:36:20,205
Here's a villus.

581
00:36:20,205 --> 00:36:21,080
This is now a villus.

582
00:36:37,840 --> 00:36:40,980
And so what happens is,
at the tip of the villus,

583
00:36:40,980 --> 00:36:45,060
cells are going to be shed from
the lining of the epithelium

584
00:36:45,060 --> 00:36:46,260
into the lumen.

585
00:36:46,260 --> 00:36:49,320
The lumen is up here.

586
00:36:49,320 --> 00:36:50,820
This is the villus.

587
00:36:50,820 --> 00:36:53,340
And the cells are going
to shed off into the lumen

588
00:36:53,340 --> 00:36:57,750
and be removed from
the organ system, OK?

589
00:36:57,750 --> 00:37:06,060
So cells are shed into
the lumen here, OK?

590
00:37:06,060 --> 00:37:09,420
And this is going to
balance the renewal

591
00:37:09,420 --> 00:37:17,040
at the base of the crypts
such that there's homeostasis.

592
00:37:17,040 --> 00:37:19,290
So I just-- the movie
I was showing you

593
00:37:19,290 --> 00:37:22,590
at the beginning of class
was a movie showing you

594
00:37:22,590 --> 00:37:25,950
what happens to a cell
undergoing apoptosis.

595
00:37:25,950 --> 00:37:29,700
So in this case, the cell
is binucleate and unhappy.

596
00:37:29,700 --> 00:37:34,410
And then you're going to see
that it basically explodes, OK?

597
00:37:34,410 --> 00:37:36,970
So that's a cell
undergoing apoptosis.

598
00:37:36,970 --> 00:37:40,950
But you see that there is a
clear change in cell morphology

599
00:37:40,950 --> 00:37:44,190
and physiology
associated with this.

600
00:37:44,190 --> 00:37:46,590
And I just want to point out
that this is also something

601
00:37:46,590 --> 00:37:49,450
that we talked about
earlier in the course.

602
00:37:49,450 --> 00:37:53,250
And we talked about experiments,
a genetic screen that

603
00:37:53,250 --> 00:37:56,340
led to the identification
of the pathway that

604
00:37:56,340 --> 00:37:58,590
regulates apoptosis.

605
00:37:58,590 --> 00:38:00,840
And that was done
by Robert Horvitz.

606
00:38:00,840 --> 00:38:05,780
Much of it was done by Robert
Horvitz in his lab here at MIT.

607
00:38:05,780 --> 00:38:10,680
And for that work, Robert
Horvitz, in addition to

608
00:38:10,680 --> 00:38:15,210
his colleagues, won
the 2002 Nobel Prize.

609
00:38:15,210 --> 00:38:17,040
So you'll recall
this is something

610
00:38:17,040 --> 00:38:20,100
we talked about in the
context of a genetic screen.

611
00:38:20,100 --> 00:38:21,720
But this is something that's--

612
00:38:21,720 --> 00:38:25,140
this is what it's doing
in your intestine system.

613
00:38:25,140 --> 00:38:29,880
It's balancing renewal so
that you have homeostasis.

614
00:38:29,880 --> 00:38:36,170
So during apoptosis, a cell goes
through a series of changes.

615
00:38:36,170 --> 00:38:38,490
First-- or what
happens eventually

616
00:38:38,490 --> 00:38:42,300
is the nucleus becomes
fragmented and chromosomal DNA

617
00:38:42,300 --> 00:38:43,560
even gets fragmented.

618
00:38:43,560 --> 00:38:45,600
It gets chopped up.

619
00:38:45,600 --> 00:38:49,710
And also, the
plasma membrane also

620
00:38:49,710 --> 00:38:54,420
starts to bleb and fragment
such that it breaks up

621
00:38:54,420 --> 00:38:58,470
into what are known as
these apoptotic bodies, OK?

622
00:38:58,470 --> 00:39:01,590
And so you can think of
these apoptotic bodies

623
00:39:01,590 --> 00:39:06,060
as bite-sized pieces of
cell that neighboring

624
00:39:06,060 --> 00:39:11,070
phagocytic cells can eat up and
remove them from the body, OK?

625
00:39:11,070 --> 00:39:13,992
So in this case, the cells
are being shed into the lumen.

626
00:39:13,992 --> 00:39:15,450
So they don't need
to get eaten up,

627
00:39:15,450 --> 00:39:18,900
because they're just going to
go out of the digestive tract.

628
00:39:27,160 --> 00:39:30,310
So there are-- cells
have numerous ways

629
00:39:30,310 --> 00:39:34,270
to activate this
apoptosis process.

630
00:39:34,270 --> 00:39:39,070
I'm going to tell you
about two types of signals

631
00:39:39,070 --> 00:39:44,000
that regulate whether or not
a cell undergoes apoptosis.

632
00:39:49,990 --> 00:39:53,410
The first is that there can be
a signal that basically tells

633
00:39:53,410 --> 00:39:58,480
the cell to kill itself, OK?

634
00:39:58,480 --> 00:40:00,580
So you can think of
this as a kill signal.

635
00:40:03,920 --> 00:40:07,060
And one type of way to
activate this signal

636
00:40:07,060 --> 00:40:10,930
is if the DNA is
irreparably damaged.

637
00:40:10,930 --> 00:40:15,550
So if there is a high
level of DNA damage,

638
00:40:15,550 --> 00:40:19,870
this induces a signaling
process in the cell.

639
00:40:19,870 --> 00:40:23,740
And one of the results
of that signal--

640
00:40:23,740 --> 00:40:26,290
in addition to regulating
the cell cycle,

641
00:40:26,290 --> 00:40:29,770
if the DNA damage
is great enough,

642
00:40:29,770 --> 00:40:32,490
it will induce an
apoptotic signal.

643
00:40:32,490 --> 00:40:37,480
And it will activate the pathway
that the Horvitz lab elucidated

644
00:40:37,480 --> 00:40:39,940
in the worm, OK?

645
00:40:39,940 --> 00:40:41,180
So there's a signal.

646
00:40:41,180 --> 00:40:45,430
And that leads to
apoptosis and death.

647
00:40:50,110 --> 00:40:54,220
Another type of signal that's
critically important for tissue

648
00:40:54,220 --> 00:40:57,290
homeostasis and determining
whether or not cells live

649
00:40:57,290 --> 00:41:01,690
or die is a survival signal.

650
00:41:01,690 --> 00:41:03,640
So there are cell
survival signals.

651
00:41:08,950 --> 00:41:13,540
And many of the growth factors,
such as EGF which you've heard

652
00:41:13,540 --> 00:41:14,410
about--

653
00:41:14,410 --> 00:41:17,740
in addition to
inducing proliferation,

654
00:41:17,740 --> 00:41:23,230
these growth factors also
tell the cell not to die, OK?

655
00:41:23,230 --> 00:41:25,285
So these could be
growth factors.

656
00:41:30,670 --> 00:41:35,830
And what these cell
survival signals do

657
00:41:35,830 --> 00:41:37,870
is they repress apoptosis.

658
00:41:41,890 --> 00:41:45,460
And so you can think
of it where you have

659
00:41:45,460 --> 00:41:49,030
a cell constantly needs
to be communicated to.

660
00:41:49,030 --> 00:41:52,660
And it needs to
be told don't die,

661
00:41:52,660 --> 00:41:55,660
don't die, don't die, don't die.

662
00:41:55,660 --> 00:41:58,330
And then if you
remove that signal,

663
00:41:58,330 --> 00:42:00,340
it won't be getting that
information anymore.

664
00:42:00,340 --> 00:42:03,430
And it can undergo
apoptosis, OK?

665
00:42:03,430 --> 00:42:06,760
So if we were to
remove this signal,

666
00:42:06,760 --> 00:42:09,400
you remove the
brakes on apoptosis.

667
00:42:09,400 --> 00:42:12,520
And the cell will
undergo cell death, OK?

668
00:42:12,520 --> 00:42:17,350
So this ensures that you
don't have a cell just kind

669
00:42:17,350 --> 00:42:19,750
of like going on and
doing its own thing,

670
00:42:19,750 --> 00:42:22,360
because cells, in
order to live, often

671
00:42:22,360 --> 00:42:25,960
need to have some sort of
signal from another cell that

672
00:42:25,960 --> 00:42:27,170
tells them to live.

673
00:42:27,170 --> 00:42:31,090
And so there's some
coordination between cells such

674
00:42:31,090 --> 00:42:33,400
that you don't have
cells rampantly

675
00:42:33,400 --> 00:42:34,675
dividing out of control.

676
00:42:40,670 --> 00:42:42,700
Now, the reason we're
doing this right

677
00:42:42,700 --> 00:42:45,460
before we talk about
cancer on Friday

678
00:42:45,460 --> 00:42:48,220
is because everything
that I'm telling you

679
00:42:48,220 --> 00:42:52,450
is really essential to
understand how a tumor is

680
00:42:52,450 --> 00:42:55,380
formed in an organ system, OK?

681
00:42:55,380 --> 00:42:57,970
And I want to end the
lecture by just planting

682
00:42:57,970 --> 00:43:01,210
a seed of an idea in your
heads before we move on

683
00:43:01,210 --> 00:43:03,940
to talk about cancer on Friday.

684
00:43:03,940 --> 00:43:07,390
And I want you to think
about the organization

685
00:43:07,390 --> 00:43:13,060
of this system, where you have
stem cells undergoing renewal.

686
00:43:13,060 --> 00:43:17,050
And then the stem cells
are just a small fraction

687
00:43:17,050 --> 00:43:19,120
of the cells in the system.

688
00:43:19,120 --> 00:43:21,070
And they're dividing slowly, OK?

689
00:43:21,070 --> 00:43:22,780
So let's think about
the stem cells.

690
00:43:25,880 --> 00:43:29,395
The DNA on the stem cells,
these are dividing slowly.

691
00:43:33,490 --> 00:43:35,230
And because they're
dividing slowly,

692
00:43:35,230 --> 00:43:37,060
they're not going
to-- their DNA is not

693
00:43:37,060 --> 00:43:40,330
going to accumulate
as many mutations.

694
00:43:40,330 --> 00:43:43,060
So there is going to
be fewer mutations.

695
00:43:46,010 --> 00:43:47,630
But these are the
cells, and this

696
00:43:47,630 --> 00:43:53,480
is the genomic DNA that is going
to stay with the organ, OK?

697
00:43:53,480 --> 00:43:57,250
So the stem cells are like
the crown jewels of the organ.

698
00:43:57,250 --> 00:44:00,950
This is the material the
organ wants to protect,

699
00:44:00,950 --> 00:44:03,380
because it's what's
going to be lasting

700
00:44:03,380 --> 00:44:08,060
in the organ the entire
lifetime of the organism, OK?

701
00:44:08,060 --> 00:44:11,750
So you get slow division
here and self-renewal.

702
00:44:11,750 --> 00:44:15,260
And this cell will
stay with the organ.

703
00:44:15,260 --> 00:44:18,200
But then where most of the
mitosis and cell division

704
00:44:18,200 --> 00:44:20,990
happens and
replication happens, it

705
00:44:20,990 --> 00:44:25,640
leads to an expansion of
cells that all differentiate.

706
00:44:25,640 --> 00:44:27,410
And because the cells
all differentiate,

707
00:44:27,410 --> 00:44:31,580
they will all eventually die and
get removed from the organ, OK?

708
00:44:31,580 --> 00:44:36,530
And this is termed
transient amplification.

709
00:44:36,530 --> 00:44:41,270
So when there's transient
amplification of one

710
00:44:41,270 --> 00:44:44,400
of the daughters
of this stem cell,

711
00:44:44,400 --> 00:44:46,025
this is where there's
rapid division.

712
00:44:49,140 --> 00:44:52,180
And where there is rapid
replication and division,

713
00:44:52,180 --> 00:44:54,580
this is where you can
get the most mutations.

714
00:44:58,390 --> 00:45:00,910
But from the
standpoint of cancer,

715
00:45:00,910 --> 00:45:02,800
that doesn't really
matter, right?

716
00:45:02,800 --> 00:45:05,320
Because in order
to have a tumor,

717
00:45:05,320 --> 00:45:07,630
the cells have to
stay in the body.

718
00:45:07,630 --> 00:45:09,490
And so all of these
cells are going

719
00:45:09,490 --> 00:45:11,740
to undergo programmed
cell death,

720
00:45:11,740 --> 00:45:14,230
and then be shed into the
lumen of the intestine

721
00:45:14,230 --> 00:45:18,190
and removed from the
organism entirely, OK?

722
00:45:18,190 --> 00:45:23,020
And so this is actually
one important way

723
00:45:23,020 --> 00:45:28,180
that our organs and our bodies
prevent tumors from happening,

724
00:45:28,180 --> 00:45:32,470
because the cell type that is
going to remain in our body

725
00:45:32,470 --> 00:45:36,460
is the one that's protected
from accumulating mutations, OK?

726
00:45:36,460 --> 00:45:38,770
And we'll come back
to this on Friday.

727
00:45:38,770 --> 00:45:40,660
And so I will see you on Friday.

728
00:45:40,660 --> 00:45:45,480
And we'll talk about
cancer on Friday.