Blood Flashcards

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1
Q

List the three sites of hemopoiesis in the body, in the order in which they occur during development.

A

1)yolk sac, 2)liver, 3)red marrow

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2
Q

What determines whether a hematopoietic stem cell develops via the lymphoid or myeloid pathway?

A

the action of lymphokines or growth factors that bind to receptors in the cell membrane of the HSC

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3
Q

Indicate whether each of the following develops via the lymphoid or myeloid pathways. a) erythrocytes

b) thrombocytes
c) neutrophils
d) monocytes e) basophils
f) eosinophils g) lymphocytes

A

a) erythrocytes (M)
b) thrombocytes (M)
c) neutrophils (M)
d) monocytes (M)
e) basophils (M)
f) eosinophils (M)
g) lymphocytes (L)

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4
Q

A typical RBC last for about ______ (time).

A

120 days

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5
Q

5) Describe the mechanism by which erythropoiesis is regulated (2 marks).

A

· the kidneys produce the hormone erythropoietin in response to low blood O2
· EPO stimulates development of erythrocytes from hematopoietic stem cells

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6
Q

Describe three cellular events that occur during erythropoiesis.

A

1) hemoglobin synthesis
2) ejection of nucleus
3) loss of organelles including mitochondria (no oxidative phosphorylation)

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7
Q

erythropoiesis is completed in about ________(time).

A

7-8 days

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8
Q

List three substances that are required in the diet for synthesis of hemoglobin.

A

1) Iron
2) Vitamin B12
3) Folic acid

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9
Q

Describe the roles of each of the following (1 mark each):

a) gastroferritin
b) transferrin
c) ferritin

A

a) a protein produced by the stomach that binds to dietary iron and assists its absorption from the small intestine
b) a blood protein that absorbs iron (mainly absorbed from intestine) and transfers it to other tissues (mainly the red bone marrow and liver)
c) a protein in the liver that binds to iron and allows it to be stored in hepatocytes until needed

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10
Q

Describe how (and where) erythrocytes are degraded (3 marks).

A
  • ageing erythrocytes are engulfed by macrophages in the spleen
  • globin is digested to form amino acids( re-used)
  • iron of heme is bound to transferrin and stored in spleen and liver
  • porphyrin of heme is converted to bilirubin and transported to liver
  • bilirubin is combined with sugars (conjugated) and released into bile
  • bilirubin is converted to yellow compounds and excreted in urine
  • or to brown compounds in the digestive tract by the action of bacteria
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11
Q

List the three main stages of hemostasis.

A
  • vascular spasm
  • formation of platelet plug
  • coagulation
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12
Q

List two chemical vasoconstrictors that are released during hemostasis and the structures
that releases them (2 marks).

A
  • thromboxanes (prostaglandins) and serotonin from platelets and
  • endothelin from damaged endothelial cells
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13
Q

Describe what platelet activation is, what causes it, and its effect (3 marks).

A
  • platelets are activated by contact with collagen
  • activation results in release of substances that cause platelets to adhere to each other and to collagen and fibrin (ADP and thromboxanes (prostaglandins)
  • a platelet plug blocks the flow of blood from a damaged vessel and forms the form for attachment of fibrin and cells (thrombus)
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14
Q

The final stage of coagulation involves the conversion of _______ to ________; a reaction
that is catalyzed by _____________.

A

a) fibrinogen
b) fibrin
c) thrombin

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15
Q

Outline the two main ways in which coagulation can be initiated (2 marks).

A
  • the release of tissue factor (III) from damaged cells

- the release of factor XII from platelets that are activated by contact with collagen

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16
Q

List four sources of coagulation factors (2 marks).

A

1) secreted into the blood by the liver
2) released into the blood by activated platelets
3) released by damaged tissues
4) calcium from diet

17
Q

Describe the roles of calcium in coagulation.

A

calcium is needed for activation of factors in both the extrinsic and intrinsic pathways; therefore it is required for coagulation to occur

18
Q

Why is factor X sometimes called the “common factor?”

A

factor X is activated by either the intrinsic or extrinsic mechanism

19
Q

Explain what clot retraction is, what causes it and the role it plays in hemostasis.

A
  • the decrease in volume of the clot due to gradual contraction of actin and myosin within platelets
  • results in edges of wound being pulled together and serum being squeezed out of clot
20
Q

Name two anticoagulants produced by the body and where they are produced.

A

antithrombin: produced by liver, slowly inactivates thrombin
heparin: produced by basophils and endothelial cells

21
Q

Outline the process of fibrinolysis, the molecules involved, how they are activated and the
general role of fibinolysis (3 marks).

A
  • fibrinolysis is the enzyme-catalyzed conversion of fibrin strands to soluble fibrin
  • it is catalyzed by the enzyme called plasmin
  • plasmin is formed from the plasma protein plasminogen by the action of tPA (tissue plasminogen activator)
  • tPA is released from cells of damaged tissue