lecture 32 Flashcards

1
Q

what cell types secrete interleukin 1

A

the phagocytic cells

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2
Q

inflammatory process starts with

A

the physical barrier is broken by something. Microorganisms can thus enter the body. In response to the sudden presence of these microorganisms the resident macrophages in the tissue release chemical signals which attract more cells to the infection site.

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3
Q

what is the second part of the inflammatory response

A

the neutrophils enter the blood stream from the bone marrow. move very quickly through the blood

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4
Q

whats part three of inlflammatory response

A

the neutrophils slow themselves down, so that they can enter the damaged tissue, by clinging to the capillary wall

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5
Q

as well as attracting neutrophils what do the chemical signals from tissue-resident cells do

A

these chemicals dilate the blood vessel making the capillary leakier, which makes it easier for neutrophils to pass through

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6
Q

what does vasodilation do to the inflammed area

A

the vasodilation causes an increased blood flow to that area. this increased blood flow makes the area both hotter and more red

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7
Q

whats step four of immune inflammatory response

A

the neutrophils can now squeeze through the leaky capillary walls and follow the chemical trail to the injury response.

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8
Q

what does the moving of the neutrophils to the tissue cause

A

causes the inflammation symptoms. redness, swelling and all that.

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9
Q

once the neutrophils gets to the inflammation site what do they do

A

phagocytosis

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10
Q

step one of phagocytosis by the neutrophils

A

the phagocyte adheres to the pathogen or debris.

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11
Q

whats step two of the phagocytosis by the neutrophils

A

the phagocyte forms a pseudopod that eventually engulfs the particles becoming a phagosome

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12
Q

whats step three of the phagocytosis by the neutrophils

A

the phagosome fuses with a lysosome to form a phagolysosome

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13
Q

are all myeloid cells phagocytic

A

not all of them no

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14
Q

whats step four of the phagocytosis by the neutrophils

A

toxic compunds and lysosomal enzymes destroy the pathogens in the phagosome.

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15
Q

step 5 of the phagocytosis process if it occurs

A

this doesn’t always occur, but the products of breaking down the pathogen may be exocytosis, removing the indigestible and residual materials.

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16
Q

whats in the lysosome that causes the phagocytosis response

A

There’s a low PH environment,
reactive oxygen and nitrogen intermediates. Like H2O2 and N2O2,
There are also several different hydrolytic enzymes like proteases, which break down proteins in the pathogen. Lipases which break down fats and nucleases which break down nucleic acids

17
Q

what enzymes are in a lyosome, what do they do

A

proteases- which break down proteins
lipases- things that break down fats
nucleases which break down nucleic acid

18
Q

whats complement

A

9 major proteins/protein complexes
(C1-9) which act in sequence to clear pathogens from blood and tissues

19
Q

complement enzymes are usually inactive y/n

A

yes, only when activated do they divide into the cascades

20
Q

what does the complement cascade do

A

labels pathogens for the phagocytes (opsonisation)
recruits phagocytes by chemical messengers
destroy the pathogens (lysis) punches hole in pathogen

21
Q

what are the 3 ways to trigger the complement pathway

A

classical, alternative and lectin

22
Q

describe the classical pathway

A

an antibody binds to the pathogen, which binds to the complement causing the enzyme C3 to start the amplify cascade.

23
Q

describe the alternate pathway

A

pathogen binds complement to its surface or another part of the pathogen, this triggers the amplifaction through C3

24
Q

describe the lectin pathway

A

where carbohydrate components of microbes bind to complement triggering C3 and the rest of the cascade

25
Q

what two pathways dont need the adaptive immune response

A

the alternative and the lectin, they dont need it as they dont use T cells.

26
Q

complement pathways develop what

A

c3 convertase

27
Q

C3 convertase goes onto what outcomes

A

opsonisation, destroy and recruitment

28
Q

what complement is used for opsonisation

A

C3b

29
Q

what complement is used for making MAC

A

C9

30
Q

what complement is used for recruitment processes

A

C3a and C5a

31
Q

complement is most useful against what

A

bacterial pathogens