Exam 2 Flashcards

1
Q

How do myofibers form?

A

Myoblasts fuse to become myotubes which differentiate into myofibers with satellite cells attached.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the regulatory proteins found on thin filaments?

A

Troponin and tropomyosin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are thin filaments composed of? Thick?

A

Actin. Myosin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What do myosin heads (cross-bridges) contain?

A

Actin, ATP, and ATPase binding sites.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What protein do z-discs contain? What is its function?

A

Actinin. Binds actin on thin filaments.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What determines the length of a sarcomere?

A

Length between neighboring z-discs.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the H-zone? Why is it lighter in pigment than the A band?

A

Portion of the A band that lacks myosin heads and contains no filament overlap - thick filaments only. These are the two reasons it is lighter in color.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the A band? I band?

A

The A band is a dark zone full of thick filaments. At the edges, the A band has filament overlap. The I band is a light zone full of thin filaments only. The I bands flank each z-disc.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the M-line? What moves closer to it during contraction?

A

Line in the middle of the H-zone with proteins that cross-link the thick filaments. Thin filaments move towards the M-line during contraction.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is the M-line? What moves closer to it during contraction?

A

Line in the middle of the H-zone with proteins that cross-link the thick filaments. Thin filaments move towards the M-line during contraction.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What changes occur in the sarcomere during contraction?

A

I-bands shorten, H-zone virtually disappears, and z-discs get closer together, shortening the sarcomere.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Why is there no attachment between thick and thin filaments during relaxation?

A

Regulatory proteins troponin and tropomyosin block actin binding sites.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What causes a conformational change in troponin? What does this conformation do?

A

Binding of calcium ions. The conformational change exposes the actin binding sites so the thin filament can bind to myosin heads.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What does binding of actin to the myosin head increase? Why?

A

Binding increases activity of ATP synthase. This is because actin is a cofactor.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What does the power stroke motion receive its energy from? What happens in this process?

A

Hydrolysis of ATP. Thick filaments anchor and pull the thin filaments towards the M-line. ATP releases the thin filament so the process can be repeated rapidly.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the NMJ?

A

Synapse that occurs between a motor neuron and muscle fiber.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Which neurotransmitter do synaptic vesicles in the NMJ release? How does this bind and what are its immediate affects?

A

Acetylcholine (AcH). Binds to AcH receptors on myofibers and causes a wave of depolarization.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What composes a triad? What are the functions of each component?

A

Composed of a t-tubule with 2 terminal cisternae (flanking SR). The t-tubule invaginates into the sarcolemma to allow for depolarization of inner myofibrils while the SR releases calcium ions that can bind to actin sites on thin filaments for contraction.

19
Q

What are the key features of slow twitch muscles? Fast twitch?

A

Slow twitch have lots of myoglobin (more red) and fatigue slowly while fast twitch are very large and fatigue rapidly.

20
Q

What are the 4 unique features of cardiac muscles in comparison to skeletal?

A
  1. Intercalated discs: allow for synchronous contraction via gap junctions/desmosomes.
  2. Branched.
  3. Uninucleated or binucleated.
  4. Diads: cardiac muscles don’t need as much calcium from the SR so they only need 1 terminal cisternae. In addition, the diads are found over z-discs compared to skeletal where they are found in the I-A region.
21
Q

What are the components of the blood and what percentage do they make up?

A

Plasma (55%), erythrocytes (45%), and buffy coat (leukocyte and platelets - <1%)

22
Q

What are the components of plasma?

A

Water (92%), proteins (albumins, globulens, and fibrinogen - 7%), and small molecules (<1%).

23
Q

What is serum? What are the serum proteins and what are their functions?

A

Plasma without clotting factors. Albumins and globulins maintain osmotic blood pressure and function as transport molecules.

24
Q

What is hematocrit?

A

Volume of packed red blood cells in a sample.

25
Q

What is the function of fibrinogen?

A

Precursor molecule to fibrin which is crucial to clotting. Clotting factors convert prothrombin into thrombin which converts fibrinogen into fibrin.

26
Q

What is the function of blood?

A

Gas carry, transportation, and clotting.

27
Q

What are blood smears?

A

Staining process that allows you to see different cells in a blood sample.

28
Q

Describe the erythrocyte structure. Include shape and size.

A

Biconcave shape that’s basically a sac of hemoglobin with no organelles or nucleus. 7-8 microns.
Hemoglobin is made up of 2 alpha globulin chains, 2 beta globulin chains, and a central heme group with iron.

29
Q

What is the function of red blood cells? How long do they live?

A

Gas transport via Hb which binds reversibly to O2 and CO2. Live for 120 days and are removed by spleen/liver by phagocytosis.

30
Q

What are sickle cell erythrocytes and what do they cause? Why have they not gone away from evolution?

A

Single amino acid mutation in beta chain that deforms the cell and makes it more fragile. These cells often burst (hemolysis) and/or lead to anemia (reduced O2 carrying capacity). Heterozygotes have a reduced risk of contracting malaria.

31
Q

What do all leukocytes contain? What do they stain with? What do presence of secondary granules indicate?

A

Azurophylic (primary granules) that stain light pink with azure. Indicates granulocytes if secondary granules present.

32
Q

What do all leukocytes contain? What do they stain with? What do presence of secondary granules indicate?

A

Azurophylic (primary granules) that stain blue with azure. Indicates granulocytes if secondary granules present.

33
Q

What are the different types of leukocytes and what percentage do they make up?

A

Neutrophils (50-60%), eosinophils (1-5%), basophils (<1%), lymphocytes (20-30%), monocytes (5-10%).

34
Q

Describe the structure of neutrophils and how they stain. What are Barr bodies?

A

Highly lobed nuclei. Secondary granules that stain light pink. Small appendages coming off nucleus which indicate a female.

35
Q

What is the function of neutrophils? Where are they often found?

A

Contains lysozymes, lactoferrin, and myeloperoxidase that all generate reactive O2 species which fight off pathogens and bacteria. Found in wound pus.

36
Q

Describe the structure of eosinophils.

A

Bi-lobed nuclei with secondary granules that stain hot pink and have an inner core and outer region.

37
Q

What is the function of eosinophils?

A

Core of secondary granules contain a protein which is toxic while RNAses and EPs on the outside act as antivirals and reactive O2 species. These cells attack large helmin (worm) parasites and can contribute to inflammation. They can worsen asthma and eosonophilic esophagitis (closing of the esophagus).

38
Q

Describe the structure of basophils.

A

Have abundant metachromatic secondary granules which stain dark blue and/or purple.

39
Q

What is the function of basophils?

A

Granules contain heparin (prevents clotting) and histamine (allergic response). Both basophils and mast cells function in allergic reactions due to their metachromatic granules.

40
Q

Describe the structure of lymphocytes including diameter.

A

Smallest leukocyte (8-9 microns) that have a very large nuclei that takes up most of the cell.

41
Q

Describe the structure, size, and function of monocytes.

A

Largest leukocyte (20-25 microns) with an indented nucleus. They are the precursor to the phagocytic system as they give rise to macrophages.

42
Q

Describe the structure of platelets.

A

No nucleus with many synthetic organelles. Platelets are fragments of megakaryotes and they are metabolically active. They are composed of alpha and delta granules.

43
Q

What is the function of platelets?

A

Crucial in the clotting process.