Week 11 - Blood Flashcards

1
Q

What percent of body mass is the blood?

A

8% - 4-6 Litres

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2
Q

What are the main proteins in plasma and their percentage?

A
  • Albumin 58%
  • Globulins 38%
  • Fibrinogen 4%
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3
Q

How big is a red blood cell?

A

8 Microns

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4
Q

Give the order of WBC and their percentage within the blood from highest to lowest

A
Neutrophils - 50-70%
Lymphocytes - 20 - 30%
Monocytes - 2 - 8%
Eosinophils - 2 - 4%
Basophils - < 1%
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5
Q

What percent RBC do men and women have?

A

Men - 40-54%

Women - 38-46%

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6
Q

What is polycythemia ?

A

Too many RBC which increases blood viscosity

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7
Q

What BC are derived from the myeloid stem?

A

Myeloblast - Basophil, neutrophil, eosinophil and Monocyte - macrophage and dendritic cells
Megakaryocyte - Thromboyles
Erythrocytes
Mast cells

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8
Q

What BC are derived from the lymphoid stem?

A

Natural Killer cells

Small Lymphocytes - T-lymphocytes, B lymphocytes- Plasma cells

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9
Q

Describe progenitor and precursor cells

A

Progenitor - won’t undergo further division

Precursor - Undergo more differentiation - not mitosis

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10
Q

What are erythropoietin and thrombopoetin associated with?

A
Erythropoeitin = RBC - Kidney
Thrombopoetin = Platelets - Liver - Increases clotting for chemotherapy patients
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11
Q

What are granulocytes used for as supplement?

A

Increases WBC formation after chemotherapy to support the immune system

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12
Q

What does iron overload lead to?

A

Tissue damage - all tissues - Fe2+ and Fe3+ binds to cells and damages them

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13
Q

Describe the globin from RBC death

A

Globin - amino acids which are reused for protein synthesis

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14
Q

Describe heme from RBC death and its metabolism in relation to iron

A

Fe3+ transferrin - Ferrin stored in the liver- then to the bone marrow via endocytosis and globin and b12 and erythropoietin - erythropoiesis to form new RBC

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15
Q

Describe heme from RBC death and its metabolism in relation to bilirubin

A

Heme - biliverdin - bilirubin in the liver - to the bile duct - bilirubin and bacteria in the small intestine -
Urobillogen to kidneys
Sterobilin to faces

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16
Q

Describe erythropoiesis

A

Pre-cursor cell type - pro erythroblast produce cells to make haemoglobin then -
Reticulocytes which eject nuclei and pass into the blood and from RBC

17
Q

What WBC type is activated by IgE ?

A

Basophils

18
Q

Describe WBC uses

A

Mast cell - dilates blood vessels + induces inflammation
Macrophage - phagocytic cell - from blood vessel to tissue
Monocyte - differentiates to macrophages- stored in the spleen and moved to infected area
Neutrophil - first responders
Basophil - Defence against parasites and allergic reaction response
Eosinophil - Release toxins to kill bacteria - cause tissue damage

19
Q

Describe neutrophil migration

A
Chemotaxis 
Rolling 
L-selection 
Shed and bind to E-selection
Adhesion 
Diapedis
20
Q

Describe the complete blood count and what high / low levels indicate

A
Neutrophils - 
High - infection 
Low - radiation exposure/ lupus 
Lymphocyte -
High - viral incfection, some leukaemia 
Low - Prolonged illness and immunosuppression 
Monocyte -
High - Viral/fungal infection, TB
Low - Bone marrow suppression 
Eosinophils - 
High - allergic reactions, parasites 
Low - drug toxicity and stress
Basophils - 
High - allergic reactions and leukaemia 
Low - Pregnancy, ovulation and stress
21
Q

Describe platelet formation

A

Controlled by thrombopoetin

Haemopoetic stem cells - megakaryoblasts - megakaryocytes - platelets

22
Q

What are the three steps for platelet formation?

A

Activation
Adhesion
Aggregation

23
Q

What is haemostasis?

A

Vascular spasm
Platelet plug formation
Blood Clotting

24
Q

Describe platelet use and formation of a blood clot upon damage

A
  • Damage to endothelial cells
  • Sub epithelial scaffolding occurs
  • Collagen and von willeband factor causes platelets to bind and starts activation process
  • Secretion by platelets - dense granules, serotonin and ADP - causes morphological changes needed for aggregation and creates cascade so increased activation of platelets
  • Fibrinogen helps activation
  • Thrombus forms involving thrombin - protease to activate fibrin
  • Forms a functional blood clot
25
Q

What are two platelet disorders?

A
  • Bernard- soulier a gene abnormality - Ib/v/IX

- GI anzmann thrombasthenia - IIb/IIIa

26
Q

Describe the intrinsic coagulation cascade

A
Damage 
- Factor 12 - 12a 
- Factor 12a initiates Factor 11 to 11a 
- Factor 11a initiates Factor 9 to 9a 
- Factor 9a initiates Factor10 to 10a
Common - 10a activates prothrombin to thrombin which activates fibrinogen to fibrin to the blood clot formation
27
Q

Describe the extrinsic coagulation cascade

A

Damage
Tissue thromboplastin activates factor 10
Common - 10a activates prothrombin to thrombin which activates fibrinogen to fibrin to the blood clot formation

28
Q

Describe vitamin K importance

A

Important in RBC production and also in cascade involved in activation in factor 10

29
Q

Describe how clots heal damage to tissue

A
  • Fibrin threads attached to the damaged surface of blood vessel contracts as platelets pull on them
  • fibrinolysis dissolves clots and disco;ved clots as sites repair
  • Inactive plasminogen is incorporated into the clot
  • Activated into plasmin by thrombin and + PA
  • Plasmin digests fibrin threads and inactivates fibrinogen, prothrombinand FV and FXII
30
Q

Describe the 4 main leukaemia types

A

Acute lymphoblastic - short onset - lymphoid stem cells found in mainly children
Acute myelogenous leukaemia - all ages
Chronic lymphoblastic leukaemia - adults age 55+
Chronic myelogenous leukaemia - prolonged onset, myeloid stem cells in mostly adults