[W2] WBCs - granulocytes Flashcards

(28 cards)

1
Q

What are the two main myeloid WBC categories?

A

Granulocytes (neutrophils, eosinophils, basophils) and mononuclear phagocytes (monocytes/macrophages).

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2
Q

What are the functions of neutrophils, eosinophils, and basophils?

A

Neutrophils: kill bacteria and fungi.
Eosinophils: attack parasites, mediate allergy.
Basophils: release histamine, mediate allergic responses.

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3
Q

What is the common precursor for granulocytes?

A

CFU-GM (colony-forming unit–granulocyte, monocyte).

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4
Q

What are the stages of granulocyte maturation?

A

Blast → Promyelocyte → Myelocyte → Metamyelocyte → Band form → Mature cell.

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5
Q

How long do neutrophils circulate?

A

~7 hours in blood, then ~20 hours in tissue before apoptosis.

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6
Q

What is the lifespan of eosinophils and basophils?

A

Eosinophils: 8–12h in blood, 8–12d in tissue.
Basophils: 2–3 days in circulation.

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7
Q

Name the 3 types of neutrophil granules and their function.

A

Primary: Microbicidal (e.g. myeloperoxidase).
Secondary: Enzymatic (e.g. lysozyme, collagenase).
Tertiary: Degradative (e.g. gelatinase, cathepsin).

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8
Q

What are the two key neutrophil actions in infection?

A

Chemotaxis and phagocytosis.

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9
Q

What is chemotaxis?

A

Directed neutrophil movement toward infection via gradients (e.g. C5a, LTB4).

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10
Q

What is needed for successful phagocytosis?

A

Opsonisation with IgG/IgM/complement and receptor binding.

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11
Q

What are the two killing mechanisms inside phagosomes?

A

O₂-dependent (e.g. hypochlorous acid from MPO).
O₂-independent (e.g. lysozyme).

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12
Q

What are neutrophil extracellular traps (NETs)?

A

DNA and enzymes extruded to trap/kill microbes outside cells.

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13
Q

What is Chronic Granulomatous Disease?

A

Inherited NADPH oxidase defect causing defective respiratory burst and granuloma formation.

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14
Q

How does myeloperoxidase deficiency affect immunity?

A

Often asymptomatic; fungi are the primary risk.

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15
Q

What is the NBT test used for?

A

Assessing neutrophil oxidative burst (e.g. in CGD).

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16
Q

What methods test neutrophil motility and phagocytosis?

A

Filter membrane assays, microscopy, and flow cytometry.

17
Q

Where are eosinophils usually found?

A

Thymus, GI tract, ovary, uterus, spleen, and lymph nodes.

18
Q

What are eosinophils’ primary functions?

A

Combat parasites and mediate allergic inflammation.

19
Q

What toxic granule contents do eosinophils release?

A

Eosinophil cationic protein, major basic protein, peroxidase, neurotoxin.

20
Q

What is Hypereosinophilic Syndrome?

A

Persistent eosinophilia >6 months, organ infiltration, possibly clonal.

21
Q

How do basophils differ from mast cells?

A

Basophils mature in marrow and circulate; mast cells mature in tissue.

22
Q

What do basophils secrete?

A

Histamine, heparin, IL-3, IL-4, IL-5, IL-13, TNF-α, GM-CSF.

23
Q

What is the Basophil Activation Test (BAT)?

A

Flow cytometry assay for allergy diagnosis (e.g. peanut allergy).

24
Q

What are the main functions of monocytes/macrophages?

A

Phagocytosis, antigen presentation, cytokine production.

25
What cytokines do monocytes produce?
IL-1, IL-6, IL-8, G-CSF, TNF-α.
26
What is the lifespan of monocytes and macrophages?
Monocytes ~24h in blood; macrophages can live months to years.
27
What causes monocytosis?
Chronic infections (e.g. TB), inflammation (e.g. Crohn’s), monocytic leukaemia.
28
What are lipid storage diseases?
Inherited disorders (e.g. Gaucher’s, Niemann-Pick) causing phagocyte accumulation of debris.