Hemostasis Introduction Part I Flashcards

1
Q

What is the converging factor between the 2 pathways?

A

factor X

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2
Q

Why is it called the extrinsic pathway?

A

requires tissue factor to function

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3
Q

Why is it called the intrinsic pathway?

A

the components are contained w/I the plasma

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4
Q

How is the extrinsic pathway initiated?

A

tissue factor binds to factor VIIa

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5
Q

How is the intrinsic pathway initiated?

A

contact factors activate factor XI

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6
Q

What are the contact factors?

A

factor XII, prekallikrein, HMWK

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7
Q

What is the common pathway?

A

events after activation of factor X (the convergence)

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8
Q

Extrinsic pathway steps?

A

tissue factor binds to factor VIIa, which activates factor X, Xa with cofactor Va activates factor II to IIa, which then converts fibrinogen to fibrin

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9
Q

Intrinsic pathway steps?

A

activation of contact factors, leading to activation of factor XI, then with cofactor VIIIa, activation of factor X, then with cofactor Va, activate factor II, converting fibrinogen to fibrin, then activate factor X

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10
Q

Where are the proteins of the coagulation cascade synthesized?

A

in the liver

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11
Q

What is bleeding diathesis?

A

bleeding tendency or predisposition

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12
Q

What are the exceptions to liver production of coagulation cascade proteins?

A
  1. tissue factor (surface of many cells)

2. VWF (endothelial cells and megakaryocytes)

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13
Q

Where is tissue factor synthesized?

A

on the surface of many cells

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14
Q

Where is VWF synthesized?

A

endothelial cells and megakaryocytes

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15
Q

Where is factor VIII produced?

A

the liver, spleen, lung, kidney

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16
Q

What does the suffix “a” indicate?

A

the activated form

17
Q

Which factor has the shortest half life? Why is this important?

A

factor VII; it’s one of the first factor to deplete in disease

18
Q

Almost all of the enzymes in the coagulation cascade are _____.

A

serine proteases

19
Q

Inactive precursor proteins are called ____.

A

zymogens

20
Q

Zymogens that become active serine proteases include ____ (7).

A
  1. factor XII (12)
  2. prekallikrein
  3. factor XI (11)
  4. factor IX (9)
  5. factor X (10)
  6. factor VII (7)
  7. factor II (2- prothrombin)
21
Q

Which are the vitamin-K dependent factors? (6)

A
  1. factor II (2)
  2. factor VII (7)
  3. factor IX (9)
  4. factor X (10)
  5. anticoagulant protein C
  6. protein S
22
Q

What to the vitamin-K dependent factors have in common?

A

Gla domains that bind Ca++ to cause conformational change of protein into active form

23
Q

Why is factor XIII (13) unique? What does it do?

A

enzyme that is not a serine protease- it’s a transglutaminase; covalently links fibrin molecules together to form a stable clot

24
Q

Why are cofactors important in the coagulation cascade?

A

they initiate and accelerate enzymatic rxns by bringing components together and orienting them correctly

25
Q

Name the cofactors in the coag. cascade. (4)

A
  1. tissue factor
  2. factor VIII (8)
  3. factor V (5)
  4. HMWK
26
Q

What protein makes the actual clot?

A

fibrinogen

27
Q

What does VWF stand for?

A

von Willebrand Factor

28
Q

What does VWF do?

A

it’s the carrier protein for factor VIII (8) in the plasma

29
Q

Where is VWF produced and stored?

A

Weibel-Palade bodies in endothelial cells and in alpha-granules of platelets

30
Q

Why does VWF bind to factor VIII (8)?

A

to protect it (prolong its half life)

31
Q

What happens in VWF-deficient pts?

A

low levels of circulating factor VIII (8), leading to a bleeding disorder similar to hemophilia A

32
Q

What do enzyme complexes consist of?

A

protease + cofactor + phospholipid surface + Ca++