Blood Clotting and Immune Function Flashcards

(27 cards)

1
Q

What are granulocytes

A

Type of white blood cell that has granules in them

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2
Q

Where do granulocytes mature

A

Bone marrow

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3
Q

Name the 3 granulocytes

A

Neutrophil, Eosinophil, Basophil

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4
Q

What’s the role of neutrophil, eosinophil, basophil

A

Neutrophil - Phagocytosis
Eosinophil - parasitic infections
Basophil - Inflammation, allergic reaction

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5
Q

What are the types of macrophage

A

Tissue and stationary macrophage

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6
Q

What are tissue macrophage + examples

A

Big increase in size in tissue
Alveolar macrophage, dendritic cells

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7
Q

Examples of stationary macrophage

A

Kupffer cell -liver
Osteoclasts

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8
Q

Meaning of haemostasis

A

Stoppage of bleeding/haemorrhage

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9
Q

What are the 3 components of haemostasis

A

Contraction of injured blood vessel
Formation of platelets plug
Clot formation

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10
Q

What is released by the endothelial cells/platelets when injured

A

Endothelin

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11
Q

What is exposed when injured

A

Collogen fibre

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12
Q

What attaches to the exposed collogen during formation of platelet plug

A

Von Willebrand’s Factor

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13
Q

What activates clotting factors

A

Lipids on the surface of platelets

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14
Q

Where are clotting factors produced and what do they require in particular

A

Liver, vitamin K

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15
Q

How do clotting factors normally circulate the blood

A

As zymogens

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16
Q

What forms when fibrinogen is converted to fibrin

17
Q

What kind of reaction is clotting factors involved in

A

Cascade reaction

18
Q

What is fibrinogen

A

Plasma protein

19
Q

What converts fibrinogen into fibrin

20
Q

What’s the zymogen of thrombin

21
Q

What’s haemophilia

A

Rare, inherited bleeding disorder where blood doesn’t clot properly - lack of clotting factors

22
Q

What does haemophilia A lack and causes it

A

Lack of factors VIII - sex linked

23
Q

What does haemophilia B lack and causes it

A

X linked, lack clotting factor IX

24
Q

What’s the most common hereditary haemostatic disorder in humans and dogs

A

Von Willebrand Disease Factor VIII

25
What's crosslinking in blood clotting
When fibrin join together by chemical bonds to strengthen clot
26
What mediates crosslinking in blood clotting and what's it triggered by
Factor XIII, thrombin
27
What binds to Von Willebrand's factor during formation of platelet plug
Glycoproteins on platelets