Other Flashcards

1
Q

Function of neutrophils

A

Ingest and digest bacteria, releases ROS and enzymes

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2
Q

Function of eosinophils

A

Attacks helminths, release peroxidase, ribonuclease, deoxyribonucleases, lipase, plasminogen and major basic protein

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3
Q

Function of basophils

A

Releases heparin for anticoagulation, histamine for vasodilation

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4
Q

Function of monocytes

A

Phagocytosis, APC, cytokine production

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5
Q

Lifespan of neutrophils?

A

3-6 hour lifespan

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6
Q

Neutrophils differentiate from _____ in bone marrow (same as RBCs).

A

Myeloid precursors, takes 7-10 days

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7
Q

How long does it take until myeloid precursors differentiate into neutrophils?

A

7-10 days

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8
Q

Myeloblast

A

Minimally granulated, scant cytoplasm, prominent nucleolus (correlates with ribosomal RNA pumping out tRNA, more primitive)

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9
Q

Promyelocyte

A

Abundant primary granules

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10
Q

Myelocyte

A

Secondary or “specific” granules (for specific pathogens)

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11
Q

List stage progressions of cells maturing.

A

1) Myeloblast
2) Promyelocyte
3) Myelocyte
4) Matured non-dividing cells

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12
Q

IL-3 function/effects

A

IL-3 affects many marrow tissues and provides proliferative and survival signals.

Also stimulates the growth of multiple myeloid cell types, involved in delay type hypersensitivity.

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13
Q

GM-CSF (Granulocyte macrophage-colony stimulating factor) function

A

GM-CSF promotes proliferation and differentiation of myeloid progenitors and monocytes

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14
Q

G-CSF (Granulocyte-colony stimulating factor) function

A

G-CSF stimulates growth of neutrophilic progenitors, acts in synergy with IL-3 on primitive myeloid cells and activates mature neutrophils.

Directs negative feedback regulation.

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15
Q

Clinical use of G-CSF and GM-CSF?

A

Raises neutrophil count and reduce the incidence of sepsis

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16
Q

T and B cells histological appearance?

A

Small (slightly bigger than RBC), mononuclear cells.

Unable to distinguish T cells from B cells by morphology

17
Q

NK and CD8+ T cells histological appearance?

A

Large granular lymphocytes

18
Q

Function of platelets in thrombus formation

A

Form a haemostatic plug and initiate thrombus formation

19
Q

Thrombocytopoiesis

A

Thrombus formation

20
Q

Describe formation of hemostatic plug

A

Collagen receptor on platelets bind to collagen, release substances that attract other platelets, which release clotting agents

21
Q

How do platelets repair microscopic vascular damage that occurs daily?

A

Via VEGF, PDGF and TGF-beta release at sites of vascular injury.

22
Q

Platelets are derived from?

A

Megakaryocyte-erythryoid progenitor (MEP)

23
Q

Endomitosis

A

Keeps dividing and not separating so it becomes large (up to 128N compared to the normal 2N, huge amount of DNA)

24
Q

Platelets also bind to the ____ receptor.

A

TPO receptor (c-Mpl)

25
TPO is produced in the?
Produced in the liver and kidney - secreted constitutively
26
Once platelet is bound to the TPO receptor, what happens?
Conformational change in the homodimeric receptor stimulates the cytoplasmic tyrosine kinase JAK2 which activates the STAT-5 pathway which stimulates proliferation and differentiation of haemopoietic stem cells and megakaryocytic/platelet progenitors
27
Tyrosine kinase JAK2 activates?
Activates the STAT-5 pathway
28
Activation of STAT5 pathway stimulates?
Proliferation and differentiation of haemopoetic stem cells and megakaryotic/platelet progenitors
29
Platelets bind free TPO and degrade it, but when platelet count is low?
Less TPO removed, so more is available to stimulate megakaryocyte production
30
Composition of plasma
Mostly water (90%) and soluble clotting factors (fibrinogen; factor 13, von Willebrand factor, factor 8; vitamin K-dependent coagulation factors 2, 7, 9 and 10)
31
Plasma can last how long in storage?
1 year at -18 degrees
32
What can plasma test indicate?
- Multiple acquired coagulation factor deficiency - Inherited single plasma factor deficiency for which no coagulation factor concentrate exists - Liver failure - Massive transfusion - Thrombotic microangiopathies, diffuse alveolar haemorrhage and catastrophic anti-phospholipid syndrome
33
Group AB plasma is?
Universally compatible with all patients
34
Group O plasma is only compatible with?
Patients with group O RBCs
35
Cryoprecipitate?
This is a distilled version of the plasma clotting factors
36
RH intravenous immunoglobulin is for?
Prevention of D antigen alloimmunization
37
Therapeutic effect of RH intravenous immunoglobulin?
Therapeutic effect is thought to be caused by antibody feedback with T-cell suppression of the B-cell clone responsible for the formation of anti-D antibody