Red Blood cells Flashcards

1
Q

Where do blood cells originate

A

bone marrow

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2
Q

What are blood cells derived from

A

haemopoietic stem cells (HSC)

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3
Q

Why are HSC described as “self-renewing”

A

some daughter cells remain as HSCs so the pool is not depleted

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4
Q

What are the sites of haemopoiesis in foetus

A

Yolk sac (1-3wks) Liver (4-8wks) Bone marrow (8-adulthood)

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5
Q

Where are progenitor and HSC distributed

A

Within the bone marrow amongst mesenchymal cells, endothelial cells and the vasculature

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6
Q

What is haemopoiesis regulated by

A

genes, transcription factors, growth factors and the microenvironment

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7
Q

What happens if haemopoiesis is not regulated

A

disturb balance between proliferation and differentiation

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8
Q

What are irons main functions

A

oxygen transport in haemoglobin and mitochondrial proteins

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9
Q

What does erythrocyte function depend on

A

Integrity of membrane, haemoglobin structure and function and cellular metabolism

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10
Q

What is the red cell membrane made up of

A

made up of lipid bilayer supported by protein cytoskeleton and contains transmembrane proteins

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11
Q

Why is the red cell membrane important

A

maintains the integrity, shape and elasticity of red cell

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12
Q

What does disruption in the vertical links of red cell membrane cause

A

Hereditary spherocytosis

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13
Q

What are spherocytes

A

cells that are spherical in shape and lack central pallor

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14
Q

What causes spherocytes

A

loss of cell membrane without the loss of an equivalent amount of cytoplasm. This makes them less flexible and removed prematurely by the spleen (haemolysis)

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15
Q

What does disruption in the horizontal links of red cell membrane cause

A

Hereditary elliptocytosis

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16
Q

What is glucose-6-phosphate dehydrogenase

A

Important enzyme in the hexose monophosphate shunt which is couple to the Glutathione metabolism which protect red cells from oxidant damage

17
Q

What is 2,3-diphosphoglycerate and what does it do

A

allosteric effector produced by the Rapaport-Luebering shuttle. It binds to beta-globin chains in haemoglobin

18
Q

What are the effects of G6DP deficiency

A

Intravascular haemolysis associated with irregularly contracted cells

19
Q

What do irregularly contracted cells look like

A

Irregular in outline, smaller and lack central pallor. Contain denatured haemoglobin forming round inclusions called Heinz bodies

20
Q

What are the causes of mircocytosis

A

Defect in haem synthesis (iron deficiency). Defect in global synthesis called thalassaemia

21
Q

Types of macrocytosis

A

round, oval and polychromatic (young and immature)

22
Q

Causes of macrocytosis

A

Lack of vitamin B12 or folic acid, liver disease, haemolysis or pregnancy

23
Q

What is increased number of reticulocytes called

A

Reticulocytosis

24
Q

Why might reticulocytosis occur

A

response to bleeding or red cell destruction (body can’t keep up so produced immature cells)

25
Q

When might target cells occur

A

obstructive jaundice, liver disease, haemoglobinpathies or hyposplenism

26
Q

What do sickle cells result from

A

polymerisation of haemoglobin s which in the deoxygenation form is much less soluble than haemoglobin

27
Q

What are schistocytes

A

small fragments of red cells

28
Q

What does schistocytosis occur from

A

Shearing process caused by platelet Ruch blood clots in blood vessels