Blood Cells Flashcards

1
Q

what constitutes the cellular component of blood?

A

red blood cells, white blood cells, platelets

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2
Q

what constitutes the fluid component of blood?

A

plasma

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3
Q

what is normal haematocrit?

A

(volume of RBC in blood) 0.45

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4
Q

what is the production of blood cells and platelets throughout life called?

A

haemopoiesis

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5
Q

what are the lifespans of RBC, WBC and platelets?

A

RBC: 120 days
WBC: 6 hours
platelets: 7 - 10 days

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6
Q

where is the bone marrow in adults, children and in utero?

A

adults: skull/ribs/spine/pelvis/long bones
children: all bones
in utero: yolk sac, liver, spleen

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7
Q

what does it mean if precursor cells are found in blood?

A

the patient has leukaemia

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8
Q

what are the hormonal growth factors that stimulate proliferation and differentiation of precursors into RBC, WBC and platelets?

A

RBC: epo (erythroprotein) [produced in kidneys]
WBC: GCSF (granulocyte colony stimulating factor)
platelets: TPO

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9
Q

what is the effect of a decrease in pH on the oxygen dissociaiton curve?

A

fall in pH –> increase in concentration of H+ ions –> deoxyhaemoglobin is stabilised in T state –> less affinity for O2 –> increase in rate of O2 dissociation

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10
Q

what is the effect of an increase in temperature on the oxygen dissociation curve?

A

increase in temperature –> bond between O2 and Fe2+ is denatured –> increase in rate of O2 dissociation

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11
Q

what are the components of RBC?

A
  1. haemoglobin
  2. enzymes for glycolysis
  3. membrane to enclose haemoglobin
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12
Q

what does haemoglobin transfer O2 to when it reaches tissues?

A

myoglobin

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13
Q

what is the dominance of A,B and O antigens?

A

A and B: co-dominant

O: recessive

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14
Q

what does ‘Rhesus positive’ indicate?

A

D antigen is present

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15
Q

what is anaemia?

A

a decrease in Hb level in blood

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16
Q

what is the normal Hb level?

A

12.5 - 15.5 g/dl

17
Q

what is the condition when Hb levels are higher than normal?

A

polycythaemia

18
Q

what are causes of anaemia?

A
  1. Fe deficiency
  2. B12/folate deficiency
  3. chronic disorder
  4. haemolysis
  5. bone marrow failure/infiltration
19
Q

how is RBC size measured and what is normal size?

A

MCV = mean cell volume

normal MCV = 82 - 96 fl

20
Q

what is RBC size and quantity in Fe deficiency anaemia?

A

MCV = < 80

quantity: low Hb levels

21
Q

what are the causes of Fe deficiency anaemia?

A
  1. bleeding [occult gastrointestinal bleeding/menorrhagia]

2. dietary

22
Q

what happens to RBC in B12/folate deficiency anaemia?

A

MCV > 100 fl (macrocytic anaemia)

23
Q

how does B12 deficiency occur? how does it lead to anaemia?

A

cause 1: B12 absorption occurs at terminal ileum. For this to occur, the gastric parietal cells in the stomach must produce the intrinsic factor, as B12 must bind to intrinsic factor to be absorbed. Hence, stomach damage –> lower B12 absorption.

cause 2: autoimmune disease called pernicious anaemia –> causes antibodies to be made against gastric parietal cells (slow onset as liver has vast store of B12)

B12/folate are needed for DNA synthesis, so without B12, RBC cannot be produced

24
Q

how does folate deficiency occur?

A
  • dietary (as folate is found in fruits/vegetables)
  • malabsorption due to celiac disease
  • increased ‘demand’ for folate (due to haemolysis/anything that leads to increased cell division)
25
Q

what is haemolysis?

A

normal or increased RBC production with decreased lifespan ( < 30 days)

26
Q

what are congenital causes of haemolysis?

A
  1. membrane issues (spherocytosis)
  2. enzyme issues (pyruvate kinase/G6Pd deficiency –> RBC not stabilised)
  3. haemoglobin issues (sickle-cell disease/ thalassaemia)
27
Q

what are acquired causes of haemolysis?

A
  1. autoimmune (can be triggered by blood transfusion)
  2. mechanical (fragmentation of RBC by mechanical heart valve/intravascular thrombosis in disseminate vascular coagulation)
  3. pregnancy (Rhesus disease which HDFN)
28
Q

what are the two main types of WBC?

A

neutrophils and lymphocytes

29
Q

what do neutrophils release?

A

chemotaxins and cytokines

30
Q

what are B cells named after? What do they do?

A

bone marrow

differentiate into plasma cells that produce immunoglobins and antigen-presenting cells (APCs)

31
Q

what are T cells named after? What do they do?

A

thymus

helper T cells: help B-cells in antibody generation, recruit more cytotoxic T cells

cytotoxic T cells: kill infected cells by releasing perforins and granzymes

32
Q

what are WBC conditions?

A
  1. acute leukaemia: proliferation of precursor cells w/o differentiation –> replaces normal blood marrow cells –> anaemia, neutropenia and thrombocytopenia
  2. acute myeloblastic leukaemia (AML): malignant proliferation of myeloblasts (adults)
  3. acute lymphocytic leukaemia (ALL): malignant proliferation of the lymphoblast precursors (children)
  4. high grade lymphoma: lymphocytes in lymph nodes –> malignant –> hodgkins/non-hodgkins lymphoma –> disease of the lymph nodes that spreads to liver, spleen, bone marrow, blood
33
Q

what do platelets determine?

A

bleeding time (PT: prothrombin time)

34
Q

what cells are platelets made from?

A

megakaryocytes

35
Q

normal number of platelets?

A

140 - 400 x 10^9 / L

36
Q

what is it called when there’s fewer platelets than normal + what are the risks?

A

thrombocytopenia

cranial bleeding (increased/spontaneous)

37
Q

what is it called when there’s more platelets than normal + what are the risks?

A

thrombocytosis

arterial/venous thrombosis –> increased risk of heart attack/stroke