W1-L3-red cells Flashcards

1
Q

blood cell origin

A

bone marrow

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2
Q

blood cell derived from

A

multipotent HSC haemapoietic steam cell

differentiate into the myeloid and lymphoid stem cell

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3
Q

process of ,making blood

A

haematopoiesis

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4
Q

haemopoiesis

A

process of making blood

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5
Q

HSC characteristics

A

part of the daughter cells do not differentiate and remain as HSC
stem cells differentiate into a specific function

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6
Q

erythrocytes biconcave shape

A

allows cells to manoeuvre within small openings

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7
Q

erythropoiesis

A

occurs in response to hypoxia or anaemia
release of erythropoietin from the kidney to the bone marrow to stimulate the production of more red blood cells
another source of erythropoietin is the interstitial cells

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8
Q

haemoglobin in adults

A

2 alpha and 2 beta chain globin chains

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9
Q

haemoglobin in foetus

A

2 alpha and 2 gamma globulin chains

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10
Q

structure of haem group

A

consist of a porphyrin ring with a Fe2+ ion in the middle which binds to 1 oxygen molecule

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11
Q

where is iron absorbed?

A

in the duodenum

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12
Q

how is Fe3+ absorbed?

A

requires the use of ascorbic acid or vitamin C

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13
Q

amount iron absorbed per day from diet

A

1-2mg

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14
Q

hepcidin

A

blocks the absorption of iron in the SI and release of iron stores

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15
Q

ferroportin

A

stimulates absorption of iron in the duodenum and breakdown of iron stores

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16
Q

increased hepcidin at inflammation site cause anaemia

A

reduce amount of iron present within the red cells and therefore impair on the development of red blood cells

17
Q

dTTP synthesis

A

dependent on folic acid and vitamin B12

required for the synthesis of thymidine and therefore DNA

18
Q

vitamin B12 absorption

A

stomach: combines with IF-intrinsic factor made in gastric parietal cells
SI: B12-IF binds to receptors in the illeum

19
Q

life cycle of a red cell

A

formation in bone marrow
breakdown by reticuloendothelial macrophages in spleen
iron released from haem group and bound to transferrin, returned to bone marrow which haem group catabolism produce bilirubin excreted as bile
globin group hydrolysed to amino acids and excreted

20
Q

microcytic

A

RBC smaller size than normal

21
Q

normocytic

A

RBC normal size

22
Q

macrocytic

A

RBC larger size than normal

23
Q

macrocytes types

A

round oval and polychromasia

24
Q

hypochromia

A

larger area of central pallor

25
Q

polychromasia

A

increased blue tinge present in the RBC

26
Q

reticulocytosis

A

presence of young RBC seen as a blue colour of the cell and larger size, present as a result of bleeding or anaemia
stained with methylene blue

27
Q

anisocytosis

A

variation in size of the RBC

28
Q

poikilocytosis

A

variation in shape of the RBC

29
Q

target cell

A

presence of accumulation of haemoglobin in the area of central pallor

30
Q

sickle cells

A

presence of a sickle shape RBC, results from HBS presence in the genes
replace glutamic acid with valine and therefore less soluble than HBA

31
Q

reference range

A

carefully defined from a reference population

3 step process : particular characteristics in volunteer, analyse using instruments and techniques and statistical tests

32
Q

deficiency in the B12

A

results of inadequate intake or inadequate secretion or malabsorption

33
Q

vitamin B12 function

A

co-factor for CoA to succinyl CoA conversion to break down aa to enter Krebs cycle
co-factor to regenerate tetrahydrofolate-needed to convert dUMP to dTTP