Innate Immunity Flashcards

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1
Q

What are the two outcomes of a ligand binding to its receptor on a cell’s surface?

A
  1. A response is triggered in the cell, initiating some change.
  2. The internal portion of the receptor becomes modified.
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2
Q

Identify three structures detected by NOD-like receptors.

A
  1. Peptidoglycan
  2. Flagellin
  3. Bacterial secretions
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3
Q

Compounds recognized by TLRs anchored in the cytoplasmic membrane and facing the outside of the cell normally include which of the following?

A
  1. Lipoproteins
  2. Flagellin
  3. Peptidoglycan
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4
Q

When a cell’s cytoplasmic PRRs detect viral RNA, the cell responds by synthesizing and secreting a(n) ________.

A

Interferon

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5
Q

PRRs in a cell’s cytoplasm enable the cell to monitor ______ for signs of invasion.

A

its own internal contents

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6
Q

Why are RIG-like receptors (RLRs) located inside most cell types?

A

They represent an important early-warning system for virally infected cells, which can alert neighboring cells a virus is present.

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7
Q

NOD-like receptors (NLRs) are cytoplasmic proteins that detect microbial components. Why would a cell need detectors on the inside, rather than the outside?

A

Such detectors could alert the cell when its borders have been breached.

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8
Q

How is the lectin pathway of the complement system activated?

A

Mannose-binding lectin (MBL), which binds to certain arrangements of mannose, a monosaccharide commonly found on the surface of bacteria and fungi. Once MBL binds, it interacts to create C3 convertase, triggering the cascade.

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9
Q

How is the classical pathway of the complement system triggered?

A

When multiple antibodies bind to an antigen (creating an antigen-antibody complex), they interact with the same components involved in the lectin pathway forming a C3 convertase and triggering the cascade.

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10
Q

How is the alternative pathway of the complement system triggered?

A

C3b binds to foreign cell surfaces; other host proteins then bind to that C3b, eventually forming a C3 convertase, thereby triggering the cascade.

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11
Q

In general, a complement system protein gets activated when it ______.

A

splits into two smaller fragments

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12
Q

A cell enters an antiviral state after detecting interferons by producing inactive antiviral proteins (iAVPs). What triggers these iAVPs to become active and cause apoptosis?

A

viral dsRNA

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13
Q

Where do most cells have pattern recognition receptors (PRRs)?

A

In the cytoplasm

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14
Q

What kind of PRR monitors a cell’s surroundings?

A

TLR (toll-like receptors)

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15
Q

RIG-like receptors (RLRs) detect what specific features of dsRNA?

A
  1. Viral RNA will often form double-stranded areas, whereas eukaryotic RNA does not.
  2. Viral RNA isn’t capped at the 5’ end (as eukaryotic RNA is)–it has 5’ phosphate groups exposed instead.
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16
Q

What does MAC stand for?

A

Membrane Attack Complex

17
Q

Is C3 convertase a part of the MAC?

A

No, MACs are formed from C5b, C6, C7, C8, and C9.

18
Q

What are the 3 major protective outcomes from the complement system?

A
  1. Opsonization
  2. Inflammatory Response
  3. Lysis of foreign cells (MACs)
19
Q

What pathogens are the most susceptible to complement lysis by MACs?

A

Gram-negative bacteria

20
Q

Macrophages with increased killing power are called what?

A

activated macrophages

21
Q

Does apoptosis trigger an inflammatory response?

A

No

22
Q
A