assays for hemostasis Flashcards

1
Q

megakaryoctyes

A

develop from hemopoietic stem cells that reside in bone morrow

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

Meg-CFC (megokaryocyte colony simulating factor) then begin ____ in which the DNA replication continues but neither the nucleus nor the cell undergoes division this produces a ________ cell

A

endomitosis; polyploid

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

C-Mpl

A

TPO receptor on megokaryocytes and platelets; when TPO binds it increase platelet synthesis

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

TPO

A

thrombopoietin; stimulates platelet synthesis, made in the liver; static

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

phospholipid scaffold is important for

A

secondary coagulation factors

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

alpha2beta1

A

GP2GP3

binds collagen

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

alpha2bbeta3

A

GPIIbGPIIIa

binds fibrinogen

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

GP Ib- IX-V

A

binds von willebrand

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

GP VI

A

activates platelets by binding collagen

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

platelet plug formation (4)

A
  1. Adhesion
  2. Activation
  3. Aggregation
  4. Secretion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

adhesion

A

GP Ib- IX-V binding to VWF

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

activation

A

platelets become activated and secrete GP IIB-IIIA

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

aggregation

A

GP IIb IIIa activates fibrinogen

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

secretion

A

platelets release granular contents and potentiate clotting

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

qualitative platelet disorders can be

A

congenital or acquired

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

acquired platelet disroders

A
  1. NSAIDS and aspirin
  2. herbs
  3. myeloproliferative disease
  4. uremia
17
Q

congenital

A
  1. Bernards- GP Ib IX-V deficiency- lack of platelet adhesion
  2. Glanzmanns thrombaesthenia- GP IIb-IIIa deficiency- lack of aggregation
18
Q

platelet dysfunction symptoms

A
  • mucocutaneous bleeding

- same as primary hemostasis- epistaxis, gum bleeding, bruising, heavy menses, petechiae

19
Q

how to quantify platelet disorders

A

PFA platelet function analyzer 100; bleeding time

20
Q

what keeps platelets from sticking to normal endothelium?

A
  • NO
  • Prostacyclin
  • ecto-ADPase- chews up ADP to prevent platelet activation
21
Q

collagen

A

GP Ib IX-V

GP VI

22
Q

thrombin

A
  • most potent platelet agonist

- PAR-1 receptor bind thrombin

23
Q

thromboxane

A

COX 1 activation leads to production of thromboxane

- thromboxane receptor is GPCR

24
Q

ADP

A
  • secreted by lysed RBC and activated platelets
  • PY12 and PY1 receptors
  • GPCR
25
Q

when the spleen gets enlarged platelets like to go there to hang out instead of being in the circulation. The platelet count drops. What happens to TPO levels?

A

remain constant because spleen is technically still in the spleen

26
Q

proplatelets

A

long branching process extended by mature megokaryocytes into the sinusoidal blood vessels of the bone marrow

27
Q

vitamin K is a water/fat soluble vitamin

A

fat

28
Q

vitamin K is used to make zymogens/cofactor coagulation factors

A

zymogen

29
Q

vitamin K pro- coagulation factors

A

2, 7, 9, 10

30
Q

vitamin K anticoagulation factors

A

protein C and S

31
Q

what four effects could cause prolonged PT?

A
  1. vitamin K deficiency- lack of green leafy vegetables
  2. vitamin K inhibitors- warfarin
  3. liver disease
  4. all factors that cause prolonged TT
  5. DIC