General Flashcards

(42 cards)

1
Q

What cells give rise to platelets, erythrocytes and monocytes?

A

Haematopoietic stem cells

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

Where is the main site of haematopoiesis in a foetus?

A

Liver

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

What are the main growth factors that regulate haematopoiesis?

A

Interleukins 1-3
Stem cell factor
Erythropoietin

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

How many oxygen molecules can each haemoglobin molecule carry?

A

4

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

What are the 4 components of an erythrocytes membrane?

A

Spectrin-forms scaffold maintaining shape and integrity
Ankrytin-anchors ion channels to spectrum skeleton
Band 4.1 protein-regulates membrane stability by stabilising spectrin-actin cytoskeleton
Band 3 protein-exchanges chloride and bicarbonate ions across the membrane

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

Where are damaged erythrocytes removed from the blood?

A

The spleen

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

What class of antigens determine the blood type of a person?

A

ABO

Split into a and b antigens

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

What antibodies target non-present ABO antigens?

A

IgM

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

What is haematocrit? What are normal levels?

A

Percentage volume of erythrocytes in the blood
Women-40%
Men-45%

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

What are platelets derived from?

A

Megakarocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What regulates platelet production?

A

Thrombopoietin

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

What is the primary function of platelets?

A

Aggregation at site of wound repair to stop bleeding

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

What clotting components are required for platelet aggregation?

A

vWF

Fibrogen

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

What are the 3 types of granules found in platelets?

A

Dense-stimulate aggregation. Contain ATP calcium and 5-HT
Lambda-contain hydrolytic enzymes
Alpha-contain coagulation factors

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

What are the 4 types of phagocyte?

A

Neutrophils
Eosinophils
Basophils
Monocytes

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

What do neutrophils induce?

A

Inflammatory response

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What indicated iron deficiency anaemia?

18
Q

What is thalassemia?

A

Genetic condition

Deficient synthesis of Hb

19
Q

What is aplastic anaemia?

A

Anaemia caused by damage to bone marrow

20
Q

What is the normal structure of haemoglobin?

A

Globin in ring of 4 polypeptide chains- 2 alpha,2 beta

Haem ring with Fe2+ ion in centre

21
Q

What is different about foetal haemoglobin?

A

2 gamma chains instead of beta

22
Q

What is indicated by a rise in HbA2

A

Sickle-cell anaemia

23
Q

What are the 3 main forms of beta thalassemia?

A

Minor-mild or absent anaemia
Intermedia-moderate anaemia
Major-severe anaemia requiring regular transfusions

24
Q

What is the precursor for erythrocytes?

A

Reticulocytes

25
What do proerythroblasts divide into?
Haemoglobin synthesising cells
26
What is polycythemia?
Excess of rbcs Absolute-overproduction of rbcs - primary: due to factors increasing production - secondary: due to other conditions increasing RBC production e.g. Hypoxia Relative-apparent rise in rbcs but actually due to reduction in blood plasma
27
Clinical signs of polycythaemia
``` Breathing difficulties Dizziness Excessive bleeding Splenomegaly Headache ```
28
What is essential thrombocythaemia?
Overproduction of platelets by megakaryocytes
29
What is thrombocytopenia?
Decrease in platelet levels
30
What blood disorders are associated with mutations in the JAK2 gene?
Polycythemia Vera | Essential thrombocythaemia
31
What causes primary immunodeficiency?
Chronic granulomatous diseases
32
What causes secondary immunodeficiency?
Viral e.g. HIV/AIDs
33
Define auto inflammation
Prolonged, unwanted innate immunity
34
What is autoimmunity?
Loss or failure of self recognition
35
What is the principle site of haematopoiesis in adults?
Long bones
36
What are primary lymphoid tissues?
Sites where lymphocytes differentiate to express antigen receptors E.g. Thymus (t lymphocytes) and bone marrow (b lymphocytes)
37
What Are secondary lymphoid tissues?
Specialised sites for turning on the acquired immune response E.g. Lymph nodes, spleen, mucosal associated lymphoid tissue (MALT)
38
What do superficial lymphatics follow?
Superficial veins
39
What do deep lymphatics follow?
Main vessels e.g. Aorta
40
Where does 3/4 of lymph from the body drain into?
Left brachiocephalic vein via thoracic duct
41
Where does lymph from the upper right quadrant drain into?
Right brachiocephalic vein
42
List the main immunity cells
``` Neutrophils Monocytes Natural killer cells Mast cells Basophils Eosinophils ```