Hematopoiesis and Cell Morphology Flashcards

1
Q

Where is hematopoiesis in a fetus

A

the yolk sac, liver and spleen

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2
Q

Where is hematopoiesis in after birth

A

the bone marrow

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3
Q

What are hematopoietic tissues

A

bone marrow, lymph nodes, spleen, liver, thymus

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4
Q

What is red marrow

A

contain hematopoietic progenitors and developing cells

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5
Q

What is yellow marrow

A

inactive, mostly fat cells, macrophages and mesenchymal cells

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6
Q

What are the stromal cells in the marrow

A

endothelial, adipocytes, macrophages, lymphocytes, osteoblasts, osteoclasts

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7
Q

What is EPO

A

secreted in hypoxic states by the interstitial cells of the kidney to promote RBC production in the marrow

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8
Q

What is thrombopoietin

A

secreted by the liver and kidneys to develop megakaryocytes into platelets

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9
Q

What are cytokines

A

trigger differentiation/maturation

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10
Q

What does estrogen do in erythropoeisis

A

promotes erythropoiesis

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11
Q

What do androgens do in erythropoeisis

A

promote erythropoiesis by promoting EPO production

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12
Q

What do thyroid hormones do in erthropoiesis

A

promote erythropoiesis through increased HGB production

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13
Q

What are hematopoitic stem cells

A

cells that can self-renew to produce more HSC, mature into pluripotent or precursor cells that give rise to WBCs, RBCs and PLTs

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14
Q

What are the intrinsic factors that cause HSC differentiation

A

genes and genetic composition of the cell

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15
Q

What are the extrinsic factors that cause HSC differentiation

A

cytokines, growth hormones, hormones

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16
Q

What cells are in the stem cell pool

A

hematopoitetic stem cells

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17
Q

What cells are in the proliferation pool

A

common myeloid pregenitor, granulocyte macrophage progenitor cells, myelocytes

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18
Q

What cells are in the maturation pool

A

cells read for release into the peripheral blood (metamyeloctes, bands and segmented)

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19
Q

What are marginating cells

A

loosely lovalized to the walls of capillaries in tissues such as the liver, spleen and lung

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20
Q

What are physiological causes of leukocytosis

A

strenuous exercise, emotional stress, labour, increased epinephrine

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21
Q

What are pathological causes of leukocytosis

A

bacterial infection, neoplasms, acute hemorrhage, tissue damage, drugs and toxins, inflammatory disorders

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22
Q

What are primary lymph tissues

A

thymus, bone marrow, antigen independent maturation

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23
Q

What are secondary lymph tissues

A

spleen, lymph nodes, tonsils, mucosal lymph tissues, antigen dependent

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24
Q

Where are T cells made

A

thymus

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25
Where are B cells made
bone marrow
26
What are the CD markers for B lymphocytes
34, 45, 19, 20, 22, 24, kappa, lambda
27
What is the purpose of B lymphocytes
produce antibodies and memory cells as well as cytokines for T-cell regulation
28
What are the CD markers for T lymphocytes
34, 45, 1, 2, 3, 4, 5, 7, 8, 25
29
Where do platelets originate from
the myeloid cell line
30
What are the requirements for erythropoiesis
iron, B6, B12, folate, EPO
31
How long do RBC survive in circulation
120 days
32
What are the steps of erythropoiesis
1. begins in the bone marrow 2. reticulocytes are released into blood stream where they mature and circulate for ~120 days 3. old and damaged erythrocytes are phagocytized by macrophages in the bone marrow, liver and spleen 4. the globin is metabolized into amino acids and the cellular components are recycled 5. the heme portion is broken down into biliverdin for transport and iron binds to transferrin for transport 6. unused heme groups can be recycled or converted into bilirubin and used to make bile in the liver. Iron can be reused or transferred to ferritin for storage in the liver
33
What are transmembrane proteins of RBCs used for
transport and adhesion sites vertical membrane support signal receptors anchor bilayer to cytoskeleton
34
What are peripheral proteins of RBCs used for
lateral membrane stability and blood group proteins
35
What is cholesterol used for in RBCs
tensile strength, deformability at low temperatures, stability, anchoring proteins
36
What are phospholipids used for in RBCs
fluidity and elasticity
37
How does the RBC produce energy
the embden-meyerhoff pathway
38
What is the hexose monophosphate shunt
it prevents oxidative damage to the cell by keeping proteins and membranes functional. It also keeps iron in the ferrous state
39
What are the steps of the hexose monophosphate shunt
1. G6P is reduces NADP to NADPH using G6P dehydrogenase 2. NADPH converts glutathione to reduced glutathione 3. reduced glutathione reduces and breaks down hydrogen peroxide to water and carbon dioxide
40
What is the methemoglobin reductase pathway
maintains hemoglobin iron in the ferrous state for effective oxygen transport
41
How can ferric heme iron be treated
infusing patients with saturated oxygen or 1% methylene blue
42
What are the steps of the methemoglobin reductase pathway
1. G3P is converted to 1-3 biphosphoglycerate 2. G3P dehydrogenase reduces NADP to NADPH 3. Methemoglobin reductase uses NADH to reduce methemoglobin to hemoglobin
43
What is the Rapoport-Leubering Pathway
produces 2,3 biphosphoglycerate which competes with oxygen for the heme iron and allows oxygen to dissociate
44
What does effective hemoglobin production require
protoporphyrins, globin chains, iron
45
What are required for protoporphyrin production
glycine, succinyl CoA, vitamin B6, ALA synthase
46
Where are alpha chains used
all hemoglobin
47
Where are beta chains used
normal adult hemoglobin
48
Where are gamma chains used
embryonic, fetal and neonatal hemoglobin
49
Where are delta chains used
variant adut hemoglobin (A2)
50
Where are epsilon chains used
embryonic hemoglobin
51
Where are Zeta chains used
embryonic hemoglobin
52
What are the hemoglobin quantities at birth
60-90% HGB F 10-40% HGB A
53
What are the hemoglobin quantities from 6months - adulthood
1-2% HGB F >95% HGB A <3.5% HGB A2
54
Where is iron absorbed
the duodenum
55
In what form is iron absorbed
the ferrous form
56
How is iron usage regulated
Copper, Zinc, Transporters (hepcidine)
57
What is hemolysis
premature destruction of RBCs
58
What can cause hemolysis
defect in RBCs defect in environment
59
What are clinical features of hemolysis
pallor, lethargy, jaundice, splenomegaly, gall stones, dark urine, bone deformity, leg ulcers
60
What are lab findings of hemolysis
increased serum bilirubin increased urine urobilinogen increased fecal stercobilinogen absent serum haptoglobins increased lactate dehydrogenase reticulocytes bone marrow erythroid hyperplasia schistocytes
61
What is intravascular hemolysis
breakdown of red blood cells in circulation
62
What is extravascular hemolysis
excessive removal of red cells by the RE system in the spleen and liver