Platelets Flashcards

1
Q

what is the function of platelets?

A

haemostasis

- formation of blood clots

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2
Q

what is the lifespan of platelets?

A

7-10 days

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3
Q

where are platelets located?

A

70% bloodstream

30% spleen

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4
Q

what do platelets originate from?

A

megakaryocytes (bone marrow)

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5
Q

why are platelets not true cells?

A
  • no nucleus

- no nuclear DNA

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6
Q

what are the types of granules in platelets?

A

alpha-granules

dense granules

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7
Q

which type of granules in platelets have a high molecular weight?

A

alpha-granules

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8
Q

what types of surface receptors do platelets have?

A
  • agaonist

- adhesion

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9
Q

what is the function of agonist receptors?

A

stimulatory molecules

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10
Q

what is the function of adhesion receptors?

A

adhesion of platelets to:

  • other platelets
  • vessel walls
  • leucocytes
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11
Q

what are the main stages of formation of blood clots?

A
  1. adhesion
  2. activation
  3. aggregation
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12
Q

Describe adhesion of platelets

A
  1. Injury to blood vessel wall exposes underlying endothelium and collagen fibres
  2. Damaged endothelium releases vWF
  3. vWF binds to collagen
  4. vWF and collagen bind to receptors on platelets
  5. Collagen triggers clotting cascade
  6. Tissue factors in blood generate thrombin
  7. Thrombin converts fibrinogen to insoluble fibrin
  8. Fibrin net captures platelets to form platelet plug
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13
Q

Describe activation of platelets

A
  1. Platelet binds to collagen
  2. Glycoprotein IIb/IIIa pathway activated
  3. ADP and thromboxane A2 produced
  4. Activates other platelets
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14
Q

What does platelet activation result in?

A

morphological change on membrane surface

  • increases SA
  • prepares for aggregation
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15
Q

describe aggregation of platelets

A
  1. once activated, platelets express GP IIb/IIIa receptor
  2. receptor binds with vWF / fibrinogen
  3. fibrinogen facilitates formation of crosslinks between platelets
  4. aids platelet aggregation to form platelet plug
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16
Q

what is the function of fibrinolysis?

A

prevents excess and inappropriate clot formation

17
Q

describe the process of fibrinolysis

A
  1. Factors XIa and XIIa activate plasminogen to form plasmin

2. plasmin breaks down fibrin into fibrin-degradation products (D-dimers)

18
Q

where is plasminogen produced?

A

liver

19
Q

what do dense granules contain?

A
  • ADP

- thromboxane A2