The Immune cell Flashcards

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1
Q

How are macrophages activated?

A

Recruited as monocytes from blood
Tissue specific differentiation
Recognise Pattern Recognition Receptors or opsonic receptors

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2
Q

What pattern recognition receptors do macrophages detect?

A

CD36,
mannose receptors
dectin-1

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3
Q

How is opsonisation targetted?

A

Fc portion of antibody detected by clustered receptors
ITAM phosphorylation of Src
Syk kinase acts on Wiskott-Aldrich syndrome protein
Arp2/3 activation causes actin to form pseudopods

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4
Q

What is the process after phagocytosis?

A

Early and late endosome formation
Fusion and maturation with lysosome
Rab5/7 GTPases cause movement to perinuclear position

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5
Q

What anti-microbial properties does the phagolysosome have?

A
lactoferrin  for nutrient deprivation
defensins for permeablisation
hydrolases
ROS/NOS
Acidifcation
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6
Q

How does TB evade phagocytic degradation?

A

Inhibits Rab5
SapM hydrolyses PI3P
PI mannosides prolong endosome fusion

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7
Q

How is TB degradation induced?

A

Interferons cause autophagy

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8
Q

How does Listeria monocytogenes evade degradation?

A

Listeriolysin forms pores to release H+/Ca so no maturation

PLPs digest phagosome to release bacterium into cytosol

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9
Q

What do Cytotoxic T cells recognise?

A

MHC Class 1 molecules presenting antigens

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10
Q

How do cytotoxic T cells cause cell death?

A

Recognise MHC1
Dock with ICAM and Leukocyte Function Associated Antigen 1 which seal immunological synapse
Microtubule organising centre and secretory lysosomes polarise to synpase
SNARE mediated docking
Perforing digests cells wall to release granzymes and hydrolases

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11
Q

What diseases are associated with T killer cells?

A

Familial haemophagocytic lymphohistiocytosis Type 2 and Type 3
Griscelli Syndrome Type 2

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12
Q

What are the causes of FHL2?

A

Mutated perforin

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13
Q

What causes FHL3?

A

Mutated Munc3/4 SNARE

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14
Q

What is Griscelli syndrome?

A

Mutated Rab27a so no trafficking/exocytosis

Partial albinism observed

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