Block 3 Complement TOKA Flashcards

1
Q

What is the key site for activation of the complement system?

A

On the surface of pathogens

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2
Q

What are the 3 pathways of the complement system?

A

Classical, Lectin, and Alternative

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3
Q

What are the end results of complement activation?

A

Recruit other cells

Opsonize pathogens

Kill pathogens (MAC)

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4
Q

What effector components do all 3 complement pathways generate?

A

C3 which turns into C3a and C3b

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5
Q

How does the 1st pathway work to recruit inflammatory cells?

A

Some complements act as CHEMOATTRACTANTS to recruit phagocytic cells to sites of complement activation (chemotaxis)

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6
Q

What is the second way of protection in the complement system?

A

complement proteins bind to pathogens and opsonize them for phagocytosis

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7
Q

What is the 3rd way of protection in the complement system?

A

Killing of pathogens by creating pores in the membrane

osmotic burst (MAC)

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8
Q

How does the complement system work to activate the adaptive immune system?

A
  1. Opsonization by complements alerts APCs to target microbes
  2. B cells with complement receptors allow them to enhance response to microbes
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9
Q

Which one has the enzymatic activity? C3a or C3b

A

C3a

this is an exception, usually the b is the one w enzymatic activity

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10
Q

How are complement components of the alternative pathway designated?

A

by Factors

Ex: Factor B

Bb is the one w enzymatic activity

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11
Q

How is the classical pathway inititated?

A

By binding of C1q

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12
Q

C1q functions?

A

The first protein in the classical pathway cascade

C1q binds to the surface of a pathogen by

  1. binding directing to bacteria (Lipoteichoic acid)
  2. Binding to C reactive proteins that bind to phosphocholine on bacteria
  3. Binding to antigen-antibody complex (MOST EFFECTIVE)
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13
Q

How is the lectin pathway initiated?

A

By binding of carbohydrate-binding proteins to carbs on pathogens

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14
Q

What are the carbohydrate-binding proteins involved in the lectin pathway?

A
  1. Mannose binding lectin (MBL) (binds to mannose containing carbs on microbes)
  2. Ficolins (binds NAG on surface of microbes)
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15
Q

How is the alternative pathway initiated?

A

By binding of spontaneously derived C3b to pathogen

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16
Q

All 3 pathways lead to generation of?

A

C3 convertase

17
Q

C3 convertase functions?

A

binds to pathogen

cleaves C3 to C3b and C3a

18
Q

C3b

A

the MAIN effector molecule of the complement system

produced by C3 convertase cleaving C3 to yield C3b

acts as a OPSONIN to target pathogen for destruction

can also bind to C3 convertase to yield C5 convertase which converts C5 to C5a and C5b

19
Q

C3a

A

a mediator of inflammation

produced by C3 convertase which cleaves C3 to yield C3a and C3b

20
Q

How is C5b produced?

A

C3b binds to C3 convertase to make C5 convertase

C5 convertase then cleaves C5 to C5a and C5b

21
Q

C5b

A

initiates the last event in complement activation

made by C3b binding to C3 convertase to make C5 convertase which cleaves C5 to C5a and C5b

22
Q

What are potent activators of the classical complement pathway?

A

IgM and IgG

they bind to the antigen and allow the Fc region to be open

C1qrs binds to the Fc region

23
Q

C1q

A

binds to the Fc region on IgM and IgG on the pathogen of the classical pathway

C1q has 6 globular heads

tails of C1q have C1r and C1s

24
Q

How is C1 activated?

A

when 2 heads of C1q bind to the Fc regions of antibodies bound to the antigen

25
Q

C4b

A

attaches to the surface of the microbe or to the Ag-Ab complex

26
Q

C1s

A

cleaves C2 into C2b and C2a

C2a has the enzymatic activity (exception)