Anatomy Lecture: Cellular Level of Organization (Ch.3)

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Review of cell membrane features

Last updated 3:29 PM on 9/4/26
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28 Terms

1
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What are the 4 Functions of the Cell/Plasma Membrane?

  1. Physical Barrier

  2. Regulates Transport —>Influx, efflux [selective permeability]

  1. Communication —> variety of receptors

  2. Structural Support —> Anchoring point for cytoskeleton; junctions between cells or cell-extracellular matrix


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What are properties of a phospholipid?

  • Major membrane component

  • Amphipathic properties

    • Hydrophilic (polar) head

    • Hydrophobic (non polar) tail



<ul><li><p>Major membrane component</p></li><li><p>Amphipathic properties</p><ul><li><p>Hydrophilic (polar) head</p></li><li><p>Hydrophobic (non polar) tail</p></li></ul></li></ul><p></p><p></p>
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What are the 2 major fluid compartments and what do they contain?

  • Intracellular fluid —> Water within the cell (2/3 of all body water)

  • Extracellular fluid —> Everything outside the cells (1/3 of body water)

    • Interstitial Fluid

    • Plasma (blood)

    • Cerebrospinal Fluid


Contain:

  • Different ionic compositions

  • Same Osmotic Concentrations

  • Exchange between compartments


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Interstitial Fluid is within which fluid compartments and what is it?

  • Within the extracellular fluid compartment

  • Its the water sitting between the cells


<ul><li><p>Within the extracellular fluid compartment</p></li><li><p>Its the water sitting between the cells </p></li></ul><p></p>
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Plasma (blood) Fluid is within which fluid compartments and what is it?

  • Within the extracellular fluid compartment

  • Its the liquid part of the blood


<ul><li><p>Within the extracellular fluid compartment</p></li><li><p>Its the liquid part of the blood</p></li></ul><p></p>
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Cerebrospinal Fluid is within which fluid compartments and what is it?

  • Within the extracellular fluid compartment

  • Its the fluid surrounding the brain and spinal cord


<ul><li><p>Within the extracellular fluid compartment</p></li><li><p>Its the fluid surrounding the brain and spinal cord</p></li></ul><p></p>
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In relation to the fluid compartments in the body, what does different ionic compositions refer to?

  • It means that the two sides (intracellular & extracellular) are chemically opposite.

  • Inside cells, potassium dominates.

  • Outside, sodium and chloride dominate.

    • Cells spend energy constantly pumping sodium out and potassium in to keep it that way, and those gradients are what let nerves and muscles fire


<ul><li><p>It means that the two sides (intracellular &amp; extracellular) are chemically opposite. </p></li><li><p>Inside cells, potassium dominates. </p></li><li><p>Outside, sodium and chloride dominate. </p><ul><li><p>Cells spend energy constantly pumping sodium out and potassium in to keep it that way, and those gradients are what let nerves and muscles fire</p></li></ul></li></ul><p></p>
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In relation to the fluid compartments in the body, what does same osmotic concentration refer to?

  • It means that even though the ions differ, the total number of dissolved particles is the same everywhere, around 290 mOsm/kg.

  • Water crosses cell membranes so easily that any imbalance gets evened out almost immediately by water shifting to the more concentrated side.


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In relation to the fluid compartments in the body, what does exchange between compartments refer to?

  • It means that the compartments aren't sealed off.

  • Water and solutes move between them constantly: across cell membranes by osmosis and transport proteins, and across capillary walls by pressure.

    • This is why a change in one compartment shows up in the others. It's also why fluid can pool where it shouldn't and cause swelling.


<ul><li><p>It means that the compartments aren't sealed off. </p></li><li><p>Water and solutes move between them constantly: across cell membranes by osmosis and transport proteins, and across capillary walls by pressure. </p><ul><li><p>This is why a change in one compartment shows up in the others. It's also why fluid can pool where it shouldn't and cause swelling.</p></li></ul></li></ul><p></p>
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What are the 3 Cell-Cell Junctions?

  1. Tight Junctions

  2. Desmosomes

  3. Gap Junctions


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What is the function of Tight Junctions?

  • Prevents passage between cells (permeability barrier)


<ul><li><p>Prevents passage between cells (permeability barrier)</p></li></ul><p></p>
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What is the function of Desmosomes?

  • Anchoring Junction

    • Prevents cells from being torn apart ('“zipper”)


<ul><li><p>Anchoring Junction</p><ul><li><p>Prevents cells from being torn apart ('“zipper”)</p></li></ul></li></ul><p></p>
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What is the function of Gap Junctions?

  • Allows for communication between adjacent cells (intracellular communication)

  • Interlocking membrane proteins


<ul><li><p>Allows for communication between adjacent cells (intracellular communication)</p></li><li><p>Interlocking membrane proteins</p></li></ul><p></p>
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Function of Cell-Matrix Junctions?

  • Anchoring of cells to underlying tissues —> attaches to the matrix beneath it

  • Hemidesmosome —> name means "half a desmosome"

    • cytoskeleton fibers link to matrix proteins

    • it passes from the matrix, through the integrin, into the cell's internal skeleton. That's why an epithelium can resist shearing forces instead of tearing.


<ul><li><p>Anchoring of cells to underlying tissues —&gt; attaches to the matrix beneath it</p></li><li><p>Hemidesmosome —&gt; name means "half a desmosome"</p><ul><li><p>cytoskeleton fibers link to matrix proteins</p></li><li><p>it passes from the matrix, through the integrin, into the cell's internal skeleton. That's why an epithelium can resist shearing forces instead of tearing.</p></li></ul></li></ul><p></p>
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What are the 2 types of Membrane Transport Mechanisms?

  1. Passive

  2. Active


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What is Passive Transport and provide examples of Passive Transport?

Passive transport does not use ATP. Things move down their gradient, from high to low concentration.

  • Diffusion

    • small, nonpolar molecules (O₂, CO₂, steroids) slip straight through the lipid bilayer

  • Facilitated Diffusion —> Protein channels and carriers

    • molecule needs help crossing → Channels are pores that open and let ions through fast → Carriers bind the molecule and change shape to pass it across (slower, and they can saturate). Ex: Glucose

  • Osmosis

    • water moves toward the side with more solute, usually through aquaporins


<p>Passive transport does not use ATP. Things move down their gradient, from high to low concentration.</p><ul><li><p>Diffusion</p><ul><li><p>small, nonpolar molecules (O₂, CO₂, steroids) slip straight through the lipid bilayer</p></li></ul></li><li><p>Facilitated Diffusion —&gt; Protein channels and carriers</p><ul><li><p>molecule needs help crossing → <u>Channels</u> are pores that open and let ions through fast → <u>Carriers</u> bind the molecule and change shape to pass it across (slower, and they can saturate). Ex: Glucose</p></li></ul></li><li><p>Osmosis</p><ul><li><p>water moves toward the side with more solute, usually through aquaporins</p></li></ul></li></ul><p></p>
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What is Active Transport and provide examples of Active Transport?

Active Transport requires the use of ATP and moves things against their gradient

  • Primary

    • pump itself hydrolyzes ATP. Ex: Na⁺/K⁺-ATPase

  • Secondary → Antiporters, Symporters

    • no direct ATP use, it borrows the gradient a primary pump already built. Sodium rushing back into the cell drags another molecule along. Symporters carry both in the same direction (Na⁺ plus glucose in the gut) → antiporters swap them in opposite directions (Na⁺ in, Ca²⁺ out)

  • Vesicular —> for cargo too large for any protein: the membrane itself wraps around it

    • Endocystosis → brings material in

    • Exocytosis → a vesicle fuses with the membrane and dumps contents out

    • Transcytosis → take something in one side of the cell and release it out the other, ferrying it across an entire cell layer


<p>Active Transport requires the use of ATP and moves things against their gradient</p><ul><li><p>Primary </p><ul><li><p>pump itself hydrolyzes ATP.   Ex: Na⁺/K⁺-ATPase</p></li></ul></li><li><p>Secondary → Antiporters, Symporters</p><ul><li><p>no direct ATP use, it borrows the gradient a primary pump already built. Sodium rushing back into the cell drags another molecule along. <u>Symporters</u> carry both in the same direction (Na⁺ plus glucose in the gut) → <u>antiporters </u>swap them in opposite directions (Na⁺ in, Ca²⁺ out)</p></li></ul></li><li><p>Vesicular —&gt; for cargo too large for any protein: the membrane itself wraps around it</p><ul><li><p>Endocystosis → brings material in</p></li><li><p>Exocytosis → a vesicle fuses with the membrane and dumps contents out</p></li><li><p>Transcytosis → take something in one side of the cell and release it out the other, ferrying it across an entire cell layer</p></li></ul></li></ul><p></p>
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What are the 4 Membrane Receptors?

  1. Endocytosis

  2. Chemical (ligand)-gated ion channel

  3. Enzymes

  4. Linked to G proteins (2nd messengers)


<ol><li><p>Endocytosis</p></li><li><p>Chemical (ligand)-gated ion channel</p></li><li><p>Enzymes</p></li><li><p>Linked to G proteins (2nd messengers) </p></li></ol><p></p>
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What is Receptor-Mediated Endocytosis?

Receptor grabs its ligand and the membrane pulls the whole complex inside as a vesicle


<p>Receptor grabs its ligand and the membrane pulls the whole complex inside as a vesicle</p><p></p>
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What is Chemical (ligand) - Gated Ion Channels?

Binding pops it open and ions flood through


<p>Binding pops it open and ions flood through</p><p></p>
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What are Enzyme Receptors?

Receptor spans the membrane with a binding site outside and an enzyme domain inside. Ligand binding switches the enzyme on, and it starts modifying proteins in the cytoplasm

<p>Receptor spans the membrane with a binding site outside and an enzyme domain inside. Ligand binding switches the enzyme on, and it starts modifying proteins in the cytoplasm</p>
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What are G-Protein Coupled Membrane Receptors?

Binding activates a G protein sitting on the inner surface, which in turn triggers an enzyme that produces a second messenger (cAMP, IP₃, calcium). That messenger then spreads through the cell and activates many enzymes at once

<p>Binding activates a G protein sitting on the inner surface, which in turn triggers an enzyme that produces a second messenger (cAMP, IP₃, calcium). That messenger then spreads through the cell and activates many enzymes at once</p>
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3 Types of Ion Channels:

  1. Leakage (passive) Channels —> always open

  2. Chemical (ligand)-gated Channels —> Requires chemical binding to open/close

  3. Voltage-gated Channels —> Requires membrane voltage change to open/close

When ions move, the membrane potential changes and serves as a signal to change cell function

<ol><li><p>Leakage (passive) Channels —&gt; always open</p></li><li><p>Chemical (ligand)-gated Channels —&gt; Requires chemical binding to open/close</p></li><li><p>Voltage-gated Channels —&gt; Requires membrane voltage change to open/close</p></li></ol><p>When ions move, the membrane potential changes and serves as a signal to change cell function</p>
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What type of cell-cell junctions allows communication between cells?

Gap Junctions

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What type of cell-cell junction might be found in a tissue that has force applied to it (like the external surface of the skin) and why?

Desmosomes. This is because they are the strongest lateral anchoring junction and so stretching or shearing force gets distributed rather than concentrated on individual membranes

<p>Desmosomes. This is because they are the strongest lateral anchoring junction and so stretching or shearing force gets distributed rather than concentrated on individual membranes</p>
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What would be the advantage of receptor-mediated endocytosis over pinocytosis?

Selectivity and concentration.

  • Pinocytosis is nonspecific the cell just sips extracellular fluid and takes in whatever happens to be dissolved in it, so a rare molecule gets brought in only in trace amounts.

  • Receptor-mediated endocytosis uses receptors that bind one specific ligand, so the target gets concentrated on the membrane surface before the vesicle forms.

  • The cell can take up large amounts of a substance present at very low outside concentrations, and control uptake by adjusting how many receptors it displays.


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Why are membrane channels required for ions to enter/exit cells?

Because the interior of the membrane is hydrophobic. Ions are charged and stay surrounded by a shell of water molecules, so crossing the lipid core would mean stripping off that hydration shell and forcing a charged particle into a fatty, nonpolar environment

  • Channels provide a water-lined pore that lets the ion pass, avoiding contact with the lipid.

  • Channels also add selectivity and control: a given channel admits only certain ions and can be gated open or closed


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What effect does movement of a cation or anion have on the membrane potential?  (Note: You should be able to provide the specific electrical term for a membrane potential that is more positive or negative then it was at rest/before the ion movement occurred.)

The terms are depolarization (membrane becomes more positive than resting) and hyperpolarization (more negative than resting). Returning toward resting after depolarization is repolarization.

The effect depends on charge and direction:

  • Cation into the cell (Na⁺, Ca²⁺) adds positive charge inside → depolarization

  • Cation out of the cell (K⁺ leaving) removes positive charge → hyperpolarization

  • Anion into the cell (Cl⁻ entering) adds negative charge → hyperpolarization

  • Anion out of the cell removes negative charge → depolarization

So the rule is just: whatever makes the inside less negative depolarizes, whatever makes it more negative hyperpolarizes.