Cell Physiology AQ Flashcards

1
Q

Why do cells require a large surface area to volume ratio to exist?

A

The large ratio enhances a cells ability to exchange information. The larger this ratio is, the more plasma membrane there is, relative to cytosol volume, to facilitate communication between the interior of the cells and the environment.

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2
Q

Some nerves are a meter long. Do these cells defy this requirement and therefore have a low surface area to volume ratio?

A

Neurons still have a high SA/V ratio. Their large plasma membrane surface area results from their very long length.

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3
Q

Wha’s the difference in resolution between your eye and a typical laboratory compound light microscope?

A

The human eye resolution (200 um) vs. a compound light microscope (0.24 um) = 1000x = 1000 fold = 3 orders of magnitude.

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4
Q

What is the difference in resolution between a light microscope and a TEM?

A

The compound light microscope (0.24 um) vs. a TEM (0.2 nm) = 1000x = 1000 fold = 3 orders of magnitude.

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5
Q

Light micrographs are obtained by directing photons through a specimen. In general, how are TEMs and SEMs obtained?

A

TEMs fire electrons through tissues and SEMs fire electrons at the surface of tissues

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6
Q

What’s the fundamental difference in the images obtained from these two different types of microscopes?

A

The main difference is that TEMs show the ultrastructure of a specimen (for example, the organelles within a cell) whereas SEMs provide a topographical view of the specimen (for example, the surface of a cell).

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7
Q

What’s the name of the cell that can increase blood calcium levels?

A

Osteoclast.

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8
Q

What’s the alternate name for an erythroctye?

A

Red blood cell (RBC).

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9
Q

What’s the name of the cell that contains a brush border?

A

Enterocyte.

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10
Q

What’s the name of the cell that makes connective tissue in your body?

A

Fibroblast.

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11
Q

98% of a plasma membrane is lipid (most of which are phospholipids) and 2% protein. However, 50% of the weight of a plasma membrane is lipid and 50% is protein. What does this latter fact say about proteins in the membrane?

A

Membrane proteins are very large and heavy molecules compared to membrane lipids

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12
Q

How does cholesterol in the membrane affect membrane fluidity?

A

Cholesterol resists phase transitions. It helps to prevent the membrane from becoming too fluid in warm conditions, where phospholipids tend to spread apart, and helps to prevent the membrane from becoming too rigid in cold conditions, where phospholipids tend to pack tightly together.

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13
Q

If cholesterol is so important in maintaining the integrity of membranes, why is it often seen as bad for you?

A

Cholesterol is often erroneously mistaken for lipoproteins such as HDL and LDL, which are merely carriers for cholesterol. Since high levels of LDL are bad for cardiovascular health, it is often assumed that cholesterol is bad too. Too much cholesterol is indeed bad for you, but not enough cholesterol is just as bad.

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14
Q

What is the difference between an integral membrane protein and a peripheral membrane protein?

A

Integral membrane proteins span the entire membrane and have polypeptide segments that are exposed on both the p- and e-faces of the membrane. Peripheral membrane proteins are on either the e- or p- (mostly P) face of the membrane and have polypeptide segments that are partially inserted into the membrane to tether them to the membrane.

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15
Q

How does a carrier protein differ from a channel protein?

A

Carrier proteins bind a solute on one side of the membrane, which triggers a conformational change, allowing them to release the solute to the other side of the membrane. Channel proteins are hydrophilic pores in the membrane that are highly selective for a specific solute or ion.

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16
Q

What are the 3 different ways in which channels are gated in the human body?

A

Ligand-gated channels, voltage-gated channels, and mechanically-gated channels.

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17
Q

How is a plasma membrane, solely constituted of phospholipids, is inherently semipermeable?

A

The plasma membrane is inherently semipermeable due to its hydrophobic interior and hydrophilic surfaces (i.e., p- and e-faces). The plasma membrane is permeable to small, nonpolar substances and gases, but is impermeable to polar/charged molecules/ions.

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18
Q

What two things are required for anything to cross the plasma membrane?

A

: A pathway and an energy source

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19
Q

How do distance, size of solute, steepness of gradient, temperature and electrical forces influence the rate of diffusion?

A

Concentration gradients dissipate (or get less steep) with increasing distance; larger solutes diffuse slower than smaller solutes; the steeper the gradient, the faster the rate of diffusion; higher temperatures increase the rate of diffusion; electrical forces influence the rate of diffusion if the diffusing solute is polar or charged. For example, if Na+ is diffusing into the cell, it has both a chemical gradient (more Na+ on the outside of the cell than the inside) and an electrical gradient (the inside of the cell is negative and Na+ is positive).

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20
Q

What is the primary mechanism by which water crosses the lipid bilayer?

A

Through aquaporins

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21
Q

What are a few good examples of molecules that freely can pass the lipid bilayer?

A

Lipids and gases. In general, small, hydrophobic molecules.

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22
Q

What is the difference between active and passive transport?

A

Active transport utilizes the energy of ATP. Passive transport utilizes the energy of a concentration gradient.

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23
Q

What is the difference between simple diffusion and facilitated diffusion?

A

In simple diffusion, molecules cross the membrane on their own (i.e., the plasma membrane itself is the pathway). In facilitated diffusion, molecules require a transport protein to assist their movement across the bilayer (i.e., the transport protein is the pathway). In both circumstances, a concentration gradient is required as the energy source.

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24
Q

A cell is hypertonic to its environment. Will the cell crenate or swell?

A

: If a cell is hypertonic to its environment, the cell will swell up, and potentially lyse.

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25
Q

Which has a lower osmotic potential, the cytosol of the cell or the interstitial fluid?

A

The cytosol of the cell has lower osmotic potential (i.e., more dissolved solute).

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26
Q

You are a cell and on a diet. Your friend tells you that there’s this new fad diet that really helps you drop the water weight. It’s all about how much solute you eat they say. Is this diet designed for you to eat more or less solute?

A

Less.

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27
Q

You are a cell and on a diet. Your friend tells you that there’s this new fad diet that really helps you drop the water weight. It’s all about how much solute you eat they say. Is the diet designed to make you hypertonic, isotonic, or hypotonic?

A

Having less solute than your surrounding makes you hypotonic to your surrounding. Therefore, water will leave you and you will shrink (i.e., crenate).

28
Q

Where is the osmotic potential higher, around you or inside you?

A

Inside you.

29
Q

Is a glucose transporter (GLUT) a uniporter, symporter, or antiporter?

A

Uniporter, since it only transports a single solute in one direction (i.e., glucose).

30
Q

How does glucose enter your body cells?

A

Glucose transporters (GLUTs)

31
Q

How does glucose enter the cells lining your small intestine?

A

Sodium-glucose transporters (SGLTs).

32
Q

What is the stoichiometry (i.e., numbers and direction of ions transported) of the Na+/K+ pump?

A

3 Na+ out and 2 K+ in

33
Q

Can you provide a detailed explanation of secondary-active transport?

A

Secondary transport occurs due to a chemical gradient that is generated by primary active transport. One example of this is the entrance of glucose into the small intestine. The entrance of glucose into intestinal cells is coupled with the entrance of Na+ ions into the cells. SGLTs are the transporters. So, the concentration gradient of Na+ (created by the actions of the Na+/K+ pump – a primary active transporter) drags glucose into the cell. Since the SGLT does not directly use the energy of ATP, but rather the gradient of Na+ created by Na+/K+ pump, it is considered to be a secondary-active transporter.

34
Q

The pump-leak model is an extraordinarily important process in the human body. Can you explain the pump-leak model and its fundamental utility in the human body?

A

The pump-leak model essentially says that whatever is pumped out of the cell leaks back in. When Na+ leaks back into cells, like muscle cells, they contract. Often, when an ion leaks back in, it drags another solute into the cell against its concentration gradient. This is seen with the SGLT.

35
Q

Explain the process by which cholesterol enters your body cells.

A

Cholesterol enters cells via receptor-mediated endocytosis. During this process, the LDL receptors in the cell membrane will recognize and bind LDL. The plasma membrane will invaginate, forming a vesicle that contains the LDL molecules. Cholesterol will then be released into the cytosol of the cells from the LDL molecules.

36
Q

What is the difference between a resting membrane potential (RMP) and a transmembrane potential (TMP)?

A

An RMP is the transmembrane potential at which the cell is at rest.

37
Q

What is the primary mechanism responsible for a RMP?

A

K+ leak channels are primarily responsible for establishing an RMP

38
Q

What does it mean that a cell is polarized?

A

Polarized cells are more negative on the inside than on the outside.

39
Q

What is autocrine signaling?

A

Cells communicating with themselves. A cell can secrete a hormone or ligand that will bind to its own receptor and affect itself.

40
Q

What is paracrine signaling?

A

Cells communicating with other cells within the same tissue or organ. The communicating molecules (i.e., chemical messengers) are often referred to as paracrine factors.

41
Q

What is the difference between endocrine signaling and neural signaling?

A

Endocrine signaling is long-lived, slower, and has more of a global, or systemic response.
Neural signaling is more localized, rapid, and short-lived

42
Q

What Is direct contact communication?

A

Cells communicating by directly touching each other.

43
Q

What Is an example of direct contact communication?

A

Membrane proteins of a white blood cell (like a natural killer (NK) cell) binding to and interacting with the membrane proteins a tumor in the body.

44
Q

Describe a gap junction.

A

Numerous throughfare channels (i.e., gap junction channels) between adjacent cells allowing rapid communication between the cells of ions and small molecules.

45
Q

What is gap junction communication, and what is an example of this?

A

The rapid movement of ions and small molecules between adjacent cells. Cardiac or smooth muscle cells are both examples of cells that communicate via gap junctions. For example, one chamber of the heart is composed of thousands of individual cells, yet the whole chamber contracts in unison, as if it is merely one large cell.

46
Q

What is the difference between a gap junction and a gap junction channel?

A

One gap junction is made up of numerous gap junction channels. A gap junction channel is made up of two hemichannels which allow the movement of ions and small molecules between cells.

47
Q

What is the difference between connexins and connexons?

A

Connexins are small proteins which combine to form a connexon. There are six connexins that compose one connexon. Another name for a connexon is a hemichannel. Considering two adjacent cells, each cell has a connexon, which combine form a gap junction channel.

48
Q

What is the difference between endogenous and exogenous ligands?

A

In general, hydrophilic ligands bind to cell-surface receptors and hydrophobic ligands bind to intracellular receptors.

49
Q

When a hydrophobic ligand and nuclear receptor combine in the nucleus, what role does this hormone-receptor complex serve in the nucleus?

A

It serves as a transcription factor which alters gene expression of proteins.

50
Q

What is the difference between ionotropic and metabotropic receptors?

A

Ionotropic receptors are ligand-gated ion channels. When a ligand binds to this receptor, it will become a channel permissive to ions. Metabotropic rectors are ligand-gated G protein-coupled receptors. Ligand binding will activate a G protein associated with the receptor and lead to a change in the metabolism of the cell.

51
Q

What is the difference between an agonist and antagonist?

A

An agonist is any ligand that binds to a particular receptor and activates it. An antagonist binds to the same receptor, therefore blocking the agonist from binding, and thereby preventing activation of the receptor.

52
Q

A cell can modulate its response to a ligand by changing its expression of membrane receptors, also known as upregulation and downregulation. If there is a low receptor density in the membrane, and therefore a weak response to ligands, which method of modulation will the cell use?

A

Receptor upregulation.

53
Q

If there is a strong response to ligands on the outside of the cell, which method of modulation can the cell use?

A

Receptor downregulation.

54
Q

Which of these phenomena do you think might explain the tolerance that someone might develop to long-standing treatment with a particular drug, and why?

A

Receptor downregulation. Chronic, or overexposure, to drugs can stimulate cells to remove receptors from their membrane so to reduce their response to the drug.

55
Q

What is signal transduction and what is an example of this phenomenon?

A

The sequence of events linking the binding of a ligand to a receptor and the cell’s response. In other words, once the ligand has activated the receptor, the signal will then be “transduced” from the outside of the cell to the inside of the cell. A good example would be the Gs G protein-coupled pathway. When a ligand binds to the receptor, the Gs G protein activates adenylate cyclase which converts ATP into cAMP. cAMP is the second messenger that then actives the cell’s response. These steps, following the ligand-receptor binding step, are all part of the signal transduction pathway.

56
Q

What are the five major second messengers in cell signaling?

A

Ca2+, cyclic AMP (cAMP), cyclic GMP (cGMP), diacylglycerol (DAG), and inositol triphosphate (IP3).

57
Q

What is the Gs G protein-coupled receptor pathway?

A

It is a stimulatory pathway.

58
Q

What is the Gi G protein-coupled receptor pathway?

A

It is an inhibitory pathway.

59
Q

What is the Gq G protein-coupled receptor pathway?

A

The Gq pathway activates the membrane enzyme phospholipase C. Phospholipase C cleaves a membrane phospholipid into diacylglycerol (DAG) and inositol triphosphate (IP3). DAG activates protein kinase C, which phosphorylates proteins inside the cell and changes the cells function/metabolism. IP3 increase intracellular Ca2+ levels by stimulating the release of Ca2+ from the smooth endoplasmic reticulum.

60
Q

Carvedilol is a medication designed to slow your heart rate and make it easier for your heart to pump blood around your body. It does this by blocking a pathway that solely increases protein kinase A phosphorylation. What type of receptor does this drug block and what protein might have increased activity in this pathway when blocked?

A

Carvedilol blocks the Gs G protein-coupled pathway. As a result, phosphatase activity may be invariably increased.

61
Q

What are the three germ layers of an embryo and which of the four principal tissue types do each give rise to?

A

Ectoderm → external lining of the body (i.e., the skin) and the nervous system; Mesoderm → muscle tissue, connective tissue, the inside lining of blood vessels (endothelium) and body cavity membranes (mesothelium);
Endoderm → internal linings of the body.

62
Q

Why are virtually all cells of the human body within 20 µm of a capillary?

A

Diffusion is distance-limited. The further you get away from the capillary, less will be diffused.

63
Q

What are the three components of a junctional complex?

A

Tight junctions (occluding junctions), adhering junctions (belt junctions), and desmosomes.

64
Q

Which one involves actin filaments and which involves intermediate filaments?

A

Adhering junctions (or belt junctions) are associated with actin filaments, while desmosomes are associated with intermediate filaments.

65
Q

Are gap junctions part of a junctional complex and what is their function?

A

No, gap junctions are pores that let ions and small molecules move between cells. They are not involved in holding cells together, but rather allow them to communicate with one another via small ions/molecules in their cytoplasm.