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Anatomy and Physiology Chapter 3 Student Lecture Part 1
EI
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Emma Innis
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Updated Jun 8, 2024
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Chapters
00:00
Chapter 1
00:10
Chapter 2
00:16
Chapter 3
00:32
Chapter 4
00:34
Chapter 5
00:45
Chapter 6
00:47
Chapter 7
00:49
Chapter 8
01:05
Chapter 9
01:32
Chapter 10
01:36
Chapter 11
01:53
Chapter 12
01:55
Chapter 13
01:58
Chapter 14
02:11
Chapter 15
02:24
Chapter 16
02:26
Chapter 17
02:42
Chapter 18
02:45
Chapter 19
03:02
Chapter 20
03:32
Chapter 21
03:35
Chapter 22
04:42
Chapter 23
04:46
Chapter 24
04:50
Chapter 25
04:52
Chapter 26
05:25
Chapter 27
05:28
Chapter 28
07:04
Chapter 29
07:07
Chapter 30
07:29
Chapter 31
07:31
Chapter 32
07:47
Chapter 33
07:49
Chapter 34
07:51
Chapter 35
07:54
Chapter 36
08:18
Chapter 37
08:34
Chapter 38
09:25
Chapter 39
09:27
Chapter 40
09:58
Chapter 41
10:00
Chapter 42
11:26
Chapter 43
12:05
Chapter 44
12:07
Chapter 45
12:08
Chapter 46
12:11
Chapter 47
12:20
Chapter 48
12:44
Chapter 49
12:45
Chapter 50
13:41
Chapter 51
13:44
Chapter 52
14:40
Chapter 53
14:42
Chapter 54
14:45
Chapter 55
14:47
Chapter 56
Audio Transcript
Auto-generated
00:01 - 00:06
All right. So this is my chapter three student lecture video
00:07 - 00:09
and let's get started.
00:12 - 00:16
First, we have intracellular and extracellular fluids.
00:17 - 00:20
Extracellular is going to be outside of the cell.
00:20 - 00:23
The cells are submersed in this fluid and it includes interstitial fluid,
00:23 - 00:28
blood plasma cerebrospinal fluid and the extracellular matrix.
00:28 - 00:32
The sodium concentration is high and the potassium concentration is low.
00:35 - 00:38
Then we have intracellular which is inside of the cell.
00:38 - 00:41
The intracellular fluid is made of cytosol.
00:41 - 00:45
The sodium concentration is low and the potassium concentration is high
00:51 - 00:55
following that. Um let's talk about the plasma membrane.
00:55 - 00:57
So the plasma membrane is an active
00:57 - 01:01
barrier that separates intracellular and extracellular fluid
01:01 - 01:05
and it determines what can enter and leave the cell.
01:07 - 01:11
So the plasma membrane is uh made of like a lipid bilayer
01:12 - 01:15
with a water loving phosphate head
01:16 - 01:17
which would be
01:17 - 01:18
hydrophilic
01:19 - 01:23
and water hating fatty acid tails which would be hydrophobic.
01:23 - 01:27
There are also membrane proteins, lipids and carbohydrates.
01:27 - 01:30
Um The possible membrane is semi permeable which
01:30 - 01:32
means only certain things can pass through.
01:35 - 01:38
So what can pass through the membrane?
01:38 - 01:42
Only certain substances can easily pass through the plasma membrane,
01:42 - 01:46
nonpolar substances uncharged and small
01:46 - 01:49
um substances are the ones that can go through easily.
01:50 - 01:53
But proteins can help determine whether or not a substance can enter the cell.
01:59 - 02:01
So membrane proteins,
02:01 - 02:03
there are two types of membrane proteins that
02:03 - 02:06
can help determine what enters the cell.
02:06 - 02:07
Many or
02:07 - 02:10
membrane proteins have many functions.
02:12 - 02:16
Integral proteins are embedded into the cell membrane
02:16 - 02:19
and they have both hydrophobic and hydrophilic regions.
02:19 - 02:22
They function as transport proteins, enzymes and receptors.
02:22 - 02:25
But their most important function is transport.
02:28 - 02:33
Then we have peripheral proteins which are loosely attached to integral proteins.
02:33 - 02:37
And they include um filaments on the intracellular surface for
02:38 - 02:39
membrane support
02:39 - 02:41
and they function as enzymes and motor
02:42 - 02:42
proteins.
02:44 - 02:47
So functions of membrane proteins,
02:48 - 02:50
they have many functions.
02:50 - 02:54
So there's transport receptors for signal transduction, enzymatic activity,
02:54 - 02:56
cell to cell joining
02:56 - 02:57
cell to cell recognition
02:58 - 02:59
and attachment to cyto
02:59 - 03:01
skeleton and extracellular matrix.
03:03 - 03:04
First transport
03:05 - 03:07
proteins that span the membrane can create a hydrophilic
03:07 - 03:10
channel that is selective for a particular solute.
03:11 - 03:15
Some proteins break apart a TP with water that's called hydrolyzing
03:16 - 03:18
and use it as energy to pump sub
03:18 - 03:22
substances across the membrane. Like you can see on the picture to the right
03:22 - 03:28
using a TP to get substances across the membrane is like an energetic currency.
03:28 - 03:32
You kind of have to pay with a TP for something to be able to cross through.
03:36 - 03:40
Then we have um receptors for signal transduction,
03:40 - 03:43
a membrane protein on the outside of the cell may have
03:43 - 03:46
a binding site that fits the shape of a chemical messenger.
03:46 - 03:48
When connected
03:48 - 03:51
the chemical may cause a change in the shape of the protein
03:51 - 03:54
which can lead to a chain of chemical reactions within the cell.
03:54 - 03:59
Only a certain type of molecule can attach and it has to be the correct shape.
04:01 - 04:03
You can see to
04:03 - 04:04
the right here
04:05 - 04:08
that that little triangle fits perfectly within there.
04:10 - 04:11
So that would be
04:12 - 04:13
a binding site.
04:16 - 04:17
Um
04:17 - 04:22
Membrane receptor proteins serve as binding sites for chemical signals
04:22 - 04:25
and they can contact signaling cells that
04:26 - 04:28
they recognize on the cell surface.
04:31 - 04:34
Some cells binding triggers enzyme activation.
04:35 - 04:40
So maybe that little triangle going into that blue rectangle can
04:40 - 04:42
signal activation
04:51 - 04:51
lips.
04:54 - 04:56
All right enzymatic activity.
04:56 - 04:59
A membrane protein may be an enzyme with its
04:59 - 05:02
active active site exposed in the adjacent solution.
05:02 - 05:06
Several enzymes in a membrane can help catalyze steps.
05:06 - 05:10
Enzymes are specific to what chemical reaction it wants to do.
05:10 - 05:13
Each enzyme will complete a different chemical reaction.
05:15 - 05:21
So, digestive enzymes will catalyze the hydrolysis of bonds and food molecules.
05:21 - 05:25
So, since it is a digestive enzyme, that is its purpose, that is its function.
05:29 - 05:31
All right cell to cell joining.
05:31 - 05:32
So
05:32 - 05:37
there are different kinds of ways that membrane proteins can
05:37 - 05:42
connect. So there is tight junctions, desmosome and gap junctions.
05:43 - 05:45
So we have gap junction
05:45 - 05:47
off to the left of this photo. Here
05:48 - 05:49
we have desma
05:49 - 05:49
zone
05:50 - 05:50
in the middle
05:51 - 05:54
and we have tight junctions all the way to the right.
06:03 - 06:04
So for tight junctions,
06:04 - 06:08
the integral proteins on nearby cells will
06:08 - 06:11
fuse and form an impermeable junction that
06:13 - 06:14
uh
06:14 - 06:15
encircles the whole cell.
06:16 - 06:18
And it prevents most molecules from moving between cells.
06:19 - 06:25
Desmosome are rivet like cell junctions formed with when linker proteins or C
06:25 - 06:26
herons,
06:26 - 06:28
um interlock like a zipper.
06:29 - 06:32
The protein is anchored to the cell with a button like
06:32 - 06:35
area on the inside of the plasma membrane called a plaque.
06:36 - 06:40
And keratin filaments connect the plaques in intercellular
06:40 - 06:41
for strength
06:42 - 06:46
desmosome are give a little bit more, they are able to move more.
06:46 - 06:49
So it reduces the possibility of tearing.
06:50 - 06:51
Then gap junctions
06:52 - 06:54
um have transmembrane proteins
06:55 - 06:59
that form tunnels and they allow small molecules to pass from cell to cell
07:10 - 07:11
cell to cell recognition.
07:12 - 07:14
There are some glycoproteins that serve as name
07:14 - 07:18
tags that are recognized by other cells.
07:18 - 07:23
Um and proteins can tell which cells they are by this glycoprotein name tag
07:23 - 07:26
and you can tell whether or not they're foreign
07:26 - 07:28
or if they are supposed to be there.
07:33 - 07:37
Lastly. Attachment to the cytoskeleton and extracellular matrix,
07:37 - 07:40
the cytoskeleton and extracellular matrix will anchor to
07:40 - 07:43
membrane proteins and this helps maintain cell shape
07:43 - 07:47
and it fixes the location of membrane proteins and plays a role in cell movement.
07:56 - 07:59
Next, we have diffusion and osmosis.
08:00 - 08:03
So since the plasma membrane is semi permeable,
08:03 - 08:06
only certain substances can pass through
08:07 - 08:11
um substances can pass through using diffusion and osmosis
08:11 - 08:15
diffusion and osmosis both fall under the category of passive transport,
08:15 - 08:18
which means there is no energy used.
08:20 - 08:21
Diffusion
08:21 - 08:24
is the natural movement of molecules from areas
08:24 - 08:27
of high concentration to areas of low concentration.
08:28 - 08:29
There is passive transport,
08:30 - 08:33
no energy and active transport uses energy.
08:36 - 08:40
So this is an example of passive transport.
08:45 - 08:52
As you can see in any of these photos, there is not um or any of the examples to the left,
08:52 - 08:54
there is not being any A TP used,
08:55 - 08:58
which would be our energetic currency like I talked about before.
08:58 - 09:00
So there is simple diffusion where
09:01 - 09:03
the molecules just pass through from
09:04 - 09:07
uh one side to the other, no energy used.
09:08 - 09:09
Then there is this channel
09:10 - 09:11
that
09:11 - 09:15
uh molecules are passing through no energy used.
09:15 - 09:18
And then lastly, there's a carrier protein and there's not energy used.
09:18 - 09:20
On the other side of the image,
09:20 - 09:24
there is a TP being used in order for molecules to come through
09:28 - 09:30
what affects diffusion.
09:30 - 09:32
So concentration,
09:33 - 09:36
the greater the difference of concentration between two areas,
09:36 - 09:38
the faster a diffusion occurs
09:39 - 09:43
molecule size. So smaller molecules diffuse faster
09:44 - 09:45
and then temperature,
09:45 - 09:48
higher temperatures can increase kinetic energy
09:48 - 09:50
which results in faster diffusion.
09:50 - 09:54
Molecules can move closer together when the heat is increased.
10:02 - 10:03
All right. So
10:04 - 10:06
facilitated diffusion.
10:06 - 10:10
If something is preventing a molecule from crossing the
10:10 - 10:12
membrane like being too large or too polar,
10:12 - 10:15
it can use a protein or a channel to help it get through.
10:15 - 10:19
Um facilitated, basically means that it needs assistance
10:20 - 10:21
in order to pass through the membrane.
10:22 - 10:23
And with that,
10:23 - 10:28
um besides the carrier protein, there are also different types of channels
10:32 - 10:33
that go along with that.
10:34 - 10:38
So when using a protein, there's no energy use like I said before.
10:38 - 10:40
But um
10:40 - 10:42
certain hydrophobic molecules,
10:42 - 10:43
for example,
10:43 - 10:45
glucose amino acids and ions are
10:45 - 10:49
transported possibly down their concentration gradient
10:49 - 10:52
by carrier mediated facilitated diffusion.
10:53 - 10:56
The molecule will attach to a protein and it will change
10:56 - 10:59
its shape in order to help it move through the membrane
11:02 - 11:05
binding of the molecule causes the carrier to envelop it
11:05 - 11:07
like in this image down here to the right.
11:08 - 11:08
And
11:09 - 11:09
um
11:10 - 11:12
it changes shape that allows the molecule to pass through.
11:13 - 11:17
So, binding is also limited depending on how many carriers are present.
11:18 - 11:20
Then we have channel mediated dis
11:21 - 11:22
facilitated diffusion
11:24 - 11:27
and that's what we'll move to. So there's different types of channels.
11:30 - 11:31
So we have
11:36 - 11:39
three different types of channels which are
11:39 - 11:39
ligand
11:39 - 11:43
gated channels which are closed at rest and open
11:43 - 11:46
in response to binding of a specific chemical or
11:46 - 11:47
ligand
11:47 - 11:49
to a specific receptor.
11:49 - 11:52
Then we have voltage gated channels that are closed at
11:52 - 11:55
rest and respond to changes in voltage across the membrane.
11:56 - 11:59
And then we have mechanically gated channels that are open
12:00 - 12:02
and closed in response to mechanical stimulation
12:02 - 12:04
such as pressure stretch or vibration.
12:10 - 12:12
Next is osmosis.
12:13 - 12:18
So osmosis is the movement of a solvent, usually water not molecules,
12:21 - 12:25
osmolarity measures the concentration and of the total
12:25 - 12:27
number of salute particles in a solvent.
12:28 - 12:32
When salute concentration goes up, water concentration goes down and that
12:33 - 12:34
is vice versa.
12:34 - 12:37
Water moves by osmosis from areas of low
12:37 - 12:39
salute concentration
12:39 - 12:41
to high salute
12:41 - 12:42
concentration.
12:47 - 12:48
All right. So we have
12:50 - 12:53
different types of pressures. So we have hydrostatic pressure,
12:53 - 12:57
which is the outward pressure exerted on the cell side
12:57 - 12:58
of the membrane
12:58 - 13:00
caused by increases
13:00 - 13:02
in volume of the cell due to osmosis
13:02 - 13:03
osmosis.
13:03 - 13:05
Then we have osmotic pressure
13:06 - 13:08
which is inward pressure due to the tendency of water
13:08 - 13:12
to be pulled into the cell with higher osmolarity.
13:12 - 13:13
So more solvent in there.
13:16 - 13:20
So back to hydrostatic, it's the pressure of water, water building up.
13:22 - 13:26
Since the water wants to go from high concentration to low concentration
13:26 - 13:28
for osmotic,
13:28 - 13:32
um the more solutes inside the cell, the bigger pull on water to enter,
13:32 - 13:36
resulting in a higher osmotic pressure inside the cell.
13:36 - 13:39
Since the solvents want to go from high to low.
13:46 - 13:48
All right, for tonicity.
13:48 - 13:49
So,
13:49 - 13:53
tonicity is the ability of a solution to change shape
13:53 - 13:56
or tone of cells by altering the cells,
13:56 - 13:58
internal water volume.
13:58 - 14:03
So first we have an isotonic solution which is to the right of the image
14:03 - 14:06
and it has the same osmolarity as the inside of the cell.
14:06 - 14:09
The volume is not changed at all whatsoever.
14:11 - 14:14
Then we have a hypertonic solution which is to the left of the image
14:14 - 14:17
and it has a higher osmolarity than inside the cell.
14:17 - 14:20
So water flows out of the cell resulting in shrinking
14:21 - 14:22
or crenation.
14:23 - 14:24
As you can see in the image,
14:25 - 14:26
then we have
14:26 - 14:30
a hypotonic solution that has a lower osmolarity than inside of the cell.
14:30 - 14:32
So the water flows into the cell
14:32 - 14:35
which causes the cell to swell
14:35 - 14:37
and that could
14:37 - 14:38
lead to cell bursting
14:38 - 14:39
or lying.
14:50 - 14:52
All right. So now on to active transport,
14:53 - 14:55
there are two types of active transport.
14:56 - 14:59
So there's active transport and vesicular transport. Both require a.
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