Chapter 2: Cells Participate in Inflammation Flashcards

1
Q

what is luekocyte emigration?

A

large outpouring of WBC’s from the blood

proceess takes about 10 minutes

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2
Q

during inflammation, where does the emmigration occcur?

A

post cappillary venules

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3
Q

what is diapedesis?

A

passive escape of RBC’s that move outside the vessel

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4
Q

where are WBC’s located in normal laminar bllod flow?

A

in the center

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5
Q

what happens to the distribution of cells upon injury?

A

RBC’s become larger and move to center and WBC’s move to the periphy

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6
Q

what is pavementing?

A

WBC’s adherence to the endothelial cells surfaces

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7
Q

where does leukocyte emigration take place?

A

only in the post capillary venules

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8
Q

what are the 5 polymorphonuclear cells?

A

Basophil
eosinophil
neutraphil

monocytes
lyphocytes

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9
Q

What is the most common WBC?

A

neutraphil 55-60%

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10
Q

what is the life span of the neutraphil?

A

8 hrs -3 days

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11
Q

how many lobes does a neutraphil have?

A

2-5 lobes

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12
Q

which cell releases histamine?

A

basophil cell with mast cells

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13
Q

what is phagocytosis?

A

in the process of exudate, engulfment of the bacteria

exocytosis

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14
Q

which cells are professional presenting cells?

A

macrophage
monocytes
basophils
neutraphils

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15
Q

what is oxygen independent enzymes of macrophaes?

A

lysozyme
lactoferin
defensin
elastase

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16
Q

what is the fuhction of lactoferin?

A

reduces free iron necessary for mitosis in mnay bacteria

17
Q

what/where is defensins produced?

A

anitbody like substance produced in lysosomes of neutraphils

18
Q

what is the fx of elasetase?

A

degrades callogen and elastin; removes intracellualr debris

19
Q

what is oxygen dependent killing?

A

production of oxygen free radicals; hydrogen peroxide, superoxide, hydroxial radicals so called “single-oxygen”

20
Q

what is chronic granulomatous?

A

rare gentic disoer in phagocytic killing that is due to the impairment of oxygen free radicals

NADPH deficiency

x-linked plasma membrane defect

21
Q

what is chediak-Higashi syndrome?

A

defect in both motlity and degranulation

cannot go to site of inflmmation on time

cannot degranulate

22
Q

How and where is histamine released?

A

at the site of inflammation and release by mast/basophils cells in response to physical injury

Type I hypersensivity reaction

23
Q

what is the function of histamine?

A

vasodilation
increased permeability
brochospasm
increase mucous secretion

24
Q

what is the fx of anaphylotoxins?

A

3Ca and 5Ca causes degranualtion

25
Q

what is the fx of serotonine?

A

fx is similar to histamine

released after exposed to callogen in the basement membrane, ADP, thrombin

26
Q

what is the function of substance P neuropeptide

A

transmission of pain signals

regulation of blood pressure

powerful mediator of increased vascular permeability

27
Q

where is substance P produced?

A

periphal nervous and CNS

lungs and gastro-intestinal nervous tissue

28
Q

what could trigger degranulation of a mast cell?

A

cold, heat, trauma, encounter with foreign substances

29
Q

what receptor does histamine bind to?

A

H1 receptor

30
Q

who/what releases serotonin?

A

platelets when they encounter collagen in the basement membrane