Red cells Flashcards

1
Q

where do all blood cells originate from

A

bone marrow derived from a cell → multipotent haemopoietic stem cell (HSCs)

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2
Q

recall which cells are then derived from multipotent haemopoetic stem cells

A
  • lymphoid stem cells

- myeloid stem cells (→ RBCs, platelets, granulocytes + monocytes)

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3
Q

define “haemopoisis”

A
  • production of blood cells

- occurs in the bone marrow

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4
Q

haemopoisis of erythrocytes

A

multipotent lymphoid-myeloid stem cell (HSC) → myeloid stem cell → erythrocyte
-same with granulocytes, monocytes -> macrophages, megakaryocyte

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5
Q

haemopoisis of B cells, T cells + NK cells

A

multipotent lymphoid-myeloid stem cell (HSC) → lymphoid stem cell → B, T, NK cells

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6
Q

two characteristics of HSCs

A

1) they can self renew (HSCs not depleted)

2) differentiate to mature progeny (not undifferentiated but can differentiate further?)

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7
Q

define “erythropoiesis”

A

development of erythrocytes

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8
Q

stages of erythropoiesis

A

myeloid stem cell → precursor cell (erythroblasts) → erythrocytes
-gradually loses its ribosome so loses its blue colour (Stain)

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9
Q

which growth factor is needed for erythropoiesis?

A
  • erythropoietin (GP synthesised in the kidney)

- stimulated by hypoxia/anaemia → stimulates BM to produce more RBCs (haemostasis)

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10
Q

where is erythropoietin synthesised?

A

1) 90% in juxatubular interstitial cell (kidney)

2) 10% hepatocytes + interstitial cells

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11
Q

how do RBCs structure help it transport oxygen?

A
  • haemoglobin → 2-alpha + 2-beta chains
  • each chain has a haem group held in a chain porphyrin → Fe2+ can bind to 1 O2
  • 300 million Hb in each RBC
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12
Q

why is it important to have these two different chains

A

-interactions between the globing chains for the delivery of O2 to the tissues

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13
Q

what type of haemoglobin in feotuses?

A

fetal haemoglobin - 2alpha + 2 gamma chains

-facilitates transfer of O2 between mother and foetus

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14
Q

where is iron absorbed?

A

duodenum

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15
Q

what is non-haem iron?

A

Fe3+ needs action of reduction substances form absorption ie. vit C

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16
Q

why is iron homeostasis important?

A

1) excessive iron taxi to liver + heart

2) no mech to excrete iron must be kept 1-2 mg per day

17
Q

which mechanisms reduce iron levels?

A

1) bone marrow → RBC recycled
2) liver storage
3) enzymes + myoglobin production

18
Q

proteins that block release of iron for the stores?

19
Q

how does hepcidin work?

A

1) released from liver (hep)

2) targets duodenum + macrophages (ferroportin degraded as hepcidin binds)

20
Q

which two vitamins are key to produce DNA?

A

1) vitamin B12

2) folate (folic acid)

21
Q

what does a deficiency of vitamins B12 and folate affect?

A

affects all rapidly dividing cells i.e. bone marrow, epithelial surfaces, gonads

-too large cells (can’t divide as not enough DNA + anaemia)

22
Q

how is vitamin B12 absorbed?

A

1) combines with intrinsic factor (IF) in stomach

2) B12-IF binds to ileum receptors

23
Q

reasons for B12 deficiency?

A
  • intake
  • IF recreation ie autoimmune disease
  • malabsoption
24
Q

how are RBCs destroyed?

A
  • in reticuloendothelial system
  • storage form of iron in macrophages
  • transferrin transports Fe in the plasma
25
term to describe a SMALLER than normal rbc
microcyte (microcytic) e.g. polychromatic microcyte (young RBC still synthesising heamoglobin)
26
term to describe a LARGER than normal rbc
macrocyte
27
three types of macrocytes
- ovbal - round - polychromatic
28
term to describe rbcs with a larger area of central pallor
hypochromic (ie. low Hb levels) -goes with microcytosis often
29
term to describe rbcs with a blue tint when stained
polychromasia (ie. higher Hb levels such as young rbcs) -goes with macrocytosis often
30
what stain colour are reticulocytes?
- blue as higher RNA content so stains with methylene blue | - immature rbc
31
term to describe variation in rbc size
anisocytosis
32
term to describe variation in rbc shape
poikilocytosis
33
examples of poikilocytes?
sickle cell, target cells
34
how do target cells arise?
- accumulation of Hb in the central area | - due to ie liver disease, spleen removal, jaundice
35
what is the difference between symptoms and signs?
- symptoms → what patient is feeling - signs → physical finding -rbc morphology must been interpreted in relation to a patients symptoms + full blood count
36
what factors affect 'normal'?
-age, gender, ethnicity, altitude...
37
how is a reference range determined?
derived from a reference population - sample using same techniques - ie free of infection, not access alcohol, age range
38
what to look out for on a blood film?
-anaemia?/ blood count? -clinical history? blood film: -size, shape, age(polychromasia)