Lecture 4 Flashcards

1
Q
A
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2
Q

Name the 3 pathways of complement activation

A

Classical pathway

Lectin pathway

Alternative pathway

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3
Q

What is the end product common to all 3 complement pathways?

A

Membrane attack complex (MAC).

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4
Q

True or False: IgM is more efficient at initiating the classical pathway than IgG.

A

TRUE.

Because IgM is a pentamer, it does not require multiple antibodies to activate C1.

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5
Q

Which complement protein is highest in concentration in the blood?

A

C3.

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6
Q

What is the consequence of an unregulated complement system?

A

Death.

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7
Q

What is the function of the membrane attack complex (MAC)?

A

Creates a pore in a cellular membrane, leading to cellular lysis.

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8
Q

Name two mechanisms by which the complement system is regulated.

A

Substrate modulation

  • a complement protein cannot be cleaved by a protease until it first binds to another protein. Prevents unnecesary cleavage.

Fragment binding

  • complement molecules are cleaved into two parts. One part (b component) usually quickly covalently binds to a nearby surface. If it does not bind, it is quickly degraded. Limits enzyme cascades to site of infection.
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9
Q

Which complement activation pathway is reliant on the adaptive immune system?

A

Classical pathway

Requires antibodies for C1 binding.

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10
Q

True or False: The lectin and alternative pathways can be activated without the presence of antibodies.

A

TRUE

These pathways are considered as part of innate immunity.

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11
Q

True or False: Mannose is commonly found in mammalian cells.

A

FALSE.

Mannose is typically found in bacteria, fungi, and other pathogenic microbes.

The presence of mannose on a microbe initiates the lectin pathway of complement activation.

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12
Q

How many IgG molecules are required to fix complement?

A

At least 2, and they must be spaced closely together.

For this reason, approximately 10,000 IgG molecules must be bound to a cell before the complement cascade normally starts.

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13
Q

Can C1 bind to free-floating antibodies in the blood stream?

A

No.

C1 can only bind to antibodies that have been bound to an antigen.

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14
Q

What is the function of C3 convertase in the complement cascade?

A

Splits C3 into C3a and C3b.

C3a - causes increased vascular permeability and is chemotactic.

C3b - opsonization. Also binds with C3 convertase to create C5 convertase.

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15
Q

Which complement molecule is responsible for opsonization of pathogens for later recognition by phagocytic cells?

A

C3b

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16
Q

What is the general effect of complement activation on nearby vasculature?

A

Vasodilation

Increased vascular permeability

17
Q

What is the effect of calcium chelation on the complement system?

A

Inactivation.

C1 is a large complex of proteins held together by calcium. Chelating calcium effectively inactivates C1.

18
Q

What is the effect of Heparin on the complement system?

A

No effect.

Heparin is a thrombin antagonist. If added to serum, it will inactivate clotting factors, but will not affect complement.

19
Q

How might one inactivate complement in serum?

A

Calcium chelation (ex: EDTA)

-inactivates complement and clotting factors.

Heat to 56 degrees Celcius for 30 minutes

-inactivates complement but preserves antibodies.

20
Q

Describe the process occuring here.

A

Two IgG molecules are bound to a membrane. C1 has cross-linked the two IgGs, causing a conformational change in C1 to expose its active site.

21
Q

C5 convertase cleaves C5 into C5a and C5b. What are the major functions of C5a?

A

Phagocyte chemotaxis

Mast cell degranulation

Neutrophil activation

22
Q

What is the function of mannose-binding lectin (MBL)?

A

Binds to mannose molecules present on pathogen surfaces.

Functionally similary to C1. Initiates the lectin pathway of complement activation.

23
Q

What is meant by the term “terminal pathway” in terms of the complement cascade?

A

The end pathway common to all 3 complement activation pathways that results in formation of the MAC.

Once C5 is cleaved, the terminal pathway is initiated.

24
Q

What molecule is pictured here?

A

Membrane attack complex (MAC).

25
Q

How is the alternative pathway activated?

A

C3 in the plasma slowly degrades into C3a and C3b on a regular basis. If C3b binds to a microbial surface, Factor B will bind, creating a C3 convertase (different molecule, but same action as in the other 2 pathways).

This results in more C3 cleavage and activation of the complement system.

26
Q

How is the alternative pathway regulated?

A

C3 in the plasma slowly degrades into C3a and C3b on a regular basis.

Mammalian cells contain sialic acid, which binds factor H. If C3b binds to a mammalian cell, it is quickly destroyed by factors H and I.

Bacterial cells lack sialic acid. If C3b binds, the complement system is quickly activated.

27
Q

In general, what are the four biological consequences of complement activation?

A

Cell lysis

Vasodilation / Increased vascular permeability

Chemotaxis

Opsonization

28
Q

What process is pictured here?

A

C1 binding to IgM.

Note that only 1 IgM molecule is needed for C1 to bind.

29
Q

Where are complement molecules produced?

A

Liver