Ch. 2 Cells of the Immune System Flashcards

1
Q

What type of stem cell differentiates into all the blood cells needed by the body?

A

Hematopoietic stem cells

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2
Q

Multipotent

A

multiple+ able; develop into multiple types of cells

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3
Q

Hematopoiesis

A

blood+making

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4
Q

what are the two types of common progenitor cells?

A
  • Common myeloid progenitor

- common lymphoid progenitor

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5
Q

What types of cells stem from the common myeloid progenitor cells?

A
  • RBCs, platelets, granulocytes, monocytes, macrophages, dendritic cells
  • makes the most different types of cells
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6
Q

What types of cells stem from the common lymphoid progenitor cells?

A

gives rise to all B cells, T cells, NK cells, dendritic cells

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7
Q

What are the three primary ways blood cells are distinguished?

A
  • appearance and behavior
  • flow cytometry
  • fluorescence microscopy
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8
Q

Neutrophils

A
  • most common
  • nuclei stain deep purple
  • granules/cytoplasm stain lilac
  • highly motile and extremely phagocytic
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9
Q

During infection, numbers of ______ increase significantly and are recruited to the site of infection by damage cues (chemokines).

A

neutrophils

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10
Q

Eosinophils

A
  • minority (1-4%)
  • nuclei stain deep purple
  • granule contents are basic, making them attractive to eosin staining them more pink
  • motile and phagocytic
  • significant role in response to large, multicellular pathogens like parasitic worms
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11
Q

Basophils

A
  • very small minority
  • nonphagocytic and contain large cytoplasmic granules filled with acidic contents
  • stain very well with basic hematoxylin (deep purple)
  • in response to infection, they release their granules, which are filled with histamine
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12
Q

Mast cells

A
  • undifferentiated cells
  • released from the bone marrow as undifferentiated cells
  • only mature after leaving the blood and taking up residence in tissues
  • full of histamine
  • responsible for allergies; inflammation
  • phagocytose
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13
Q

Where are mast cells located?

A

in skin, CT, and mucosal epithelia in respiratory, genitourinary, and digestive tracts

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14
Q

Why is leukocytosis a sign of infection?

A

It is an increase in circulating neutrophils, which will only increase if there is infection.

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15
Q

What is the primary cell type found in pus?

A

neutrophils

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16
Q

What are NETs?

A

self sacrifice and project strands of their own DNA to ensnare pathogens

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17
Q

What is NETosis?

A

form of cell death (apoptosis of neutrophils)

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18
Q

What effects does histamine release have on the body?

A

histamine induces inflammation

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19
Q

What granulocyte is primarily responsible for allergies?

A

mast cells

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20
Q

What is the purpose of antigen-presenting cells?

A

a group of cells that function as cellular bridges between innate and adaptive immune systems

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21
Q

During antigen presentation, if a T cell is presented its _____ _____, it will activate and begin adaptive immune responses.

A

cognate antigen

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22
Q

Monocytes

A

o Make up 4-8% of leukocytes (WBC)
o Circulate in blood, but can migrate into tissues in response to infection signals
o In tissues, can further differentiate into macrophages or dendritic cells
o Large nuclei compared to other, agranulocyte

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23
Q

Macrophages

A

o Pathogens marked with soluble antibody are said to be opsonized (make tasty)
o Can very efficiently engulf opsonized pathogens
o This means that once adaptive immunity is fully activated and B cells are making antibody against a pathogen, macrophages are crazy effective and finding and destroying
o (a monocyte that has navigated to tissue)

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24
Q

Dendritic Cells

A

o Critical initiators of immune responses as a key bridge between innate and adaptive immunity
o Capture antigen just like other APCs, but their long dendritic extensions make their surface area large
 Can interact with many T cells at once, making them super activators of the adaptive immune response
 AKA: THE most important APCs
 are the most potent APC for activating naïve T cells
• Take in antigen by phagocytosis, endocytosis, and pinocytosis

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25
What cell type is responsible for forming platelets that are a necessary aspect of blood clot formation?
megakaryocytes
26
What cells are part of the lymphoid lineage?
B lymphocytes T lymphocytes NK cells
27
Where do B cells develop?
bone marrow
28
What do activated B cells do?
* Act as APC (phagocytic and can present to T cells) * Express costimulatory receptors to activate T cells * Develop into plasma cell
29
Where do T cells develop?
thymus
30
Is an NK cell an adaptive lymphocyte or an innate lymphocyte?
innate lymphocyte
31
How does an NK cell decide which cells too kill?
attacks abnormal cells that lack MHC expression
32
Where does the majority of hematopoiesis occur in a developing fetus during the first trimester?
yolk sac
33
Where does the majority of hematopoiesis occur in a developing fetus during the second trimester?
liver
34
Where does the majority of hematopoiesis occur in a developing fetus during the third trimester?
bone marrow
35
As humans age, we lose some of the areas where hematopoiesis occurs. Compare the areas that serve as hematopoiesis zones in a 10 year old, 25 year old, and a 50 year old.
10: vertebral and pelvis, tibial, sternum, ribs 25: vertebral and pelvis, sternum, ribs 50: vertebral and pelvis, sternum, ribs
36
What type of cells are present in the bone microenvironment?
HSCs reside in specialized microenvironments, or stem cell niches. Lined with supportive cells that regulate survival, proliferation, differentiation, and trafficking. • Osteoblasts  generate bone and control HSC differentiation • Endothelial cells  line blood vessels and regulate HSC differentiation • Sympathetic neurons  control release of cells from bone marrow • HSCs and progenitor development are controlled with a stream of cytokines and growth factors
37
Why does bone get less and less able to perform hematopoiesis as we age?
as we age, bone marrow is slowly converted to adipose tissue; approaches 50% and decreases hematopoiesis
38
Where do T cells develop?
T cell progenitors develop initially in the bone marrow, but then migrate to the thymus where they achieve full maturity.
39
What is negative selection of T cells?
if bind too tightly or recognize self-peptides (Kills every cell that recognizes self-molecules and will not attack body)
40
What is positive selection of T cells?
if bind “just right” ensuring they will recognize MHC. (Kills every cell that doesn’t match MHC)
41
What are the three primary secondary lymphoid organs?
- lymph nodes - spleen - X-associated lymphoid tissue
42
What do all secondary lymphoid organs have, despite their different overall anatomies?
- anatomically distinct regions of T cell and B cell activity - lymphoid follicles
43
How are SLOs connected?
via the blood and lymphatic circulatory systems
44
How much lymph fluid is returned to the circulatory system each day?
~2.9 L a day
45
What can occur when lymph is not efficiently returned to the circulatory system?
lymphedema results and effects on immune reaction are evident
46
Where do T cells enter a lymph node?
o Naïve T lymphocytes enter via the high endothelial venules of the blood stream to enter the cortex.
47
Where do B cells enter a lymph node?
through high endothelial venules (like T cells)
48
Where are T cells found when they are searching for antigen?
o They browse APCs in the paracortex (takes 16-24 hours to browse the APCs in a single lymph node)  APCs on a network of fibers created by fibroblastic reticular cells known as the fibroblastic reticular cell conduit system. • This system serves as a highway where T cells are guided by adhesion molecules and chemokines
49
Where do nonactivated lymphocytes exit?
o If they do not find their MHC peptide match, they leave via the efferent lymphatics (T cells)
50
Effector memory cells
continue to circulate among all tissues
51
Central memory cells
take up residence in secondary lymphoid organs
52
Resident memory cells
settle in nonlymphoid tissue
53
What occurs in germinal centers?
facilitate the generation of B cells with increased receptor affinity through somatic hypermutation
54
What dictates which B cells live to become effector plasma cells?
- activated b cells fight for antigen in these centers - once done, the surviving cells make even better antibodies and move to the medulla to secrete antibodies into the bloodstream - germinal centers take 4-7 days to establish and last about 3 weeks
55
Where do antigens/APCs enter the spleen?
via splenic artery
56
Where are T cells found when they are searching for antigens in the spleen?
browse APCs in PALS
57
Where are B cells found when they are searching for antigens in the spleen?
encounter antigen in follicles, find TH match, and then create germinal centers in follicles
58
Where do nonactivated lymphocytes exit the spleen?
splenic artery
59
What does NET stand for?
Neutrophil Extracellular Trap
60
How do CD4+ cells recognize antigens?
- professional APCs use MHC II to present | - browse surfaces of APCs with TCRs looking for matching antigen (if found become subset of T cells)
61
How do CD8+ cells recognize antigens?
-somatic cells use MHC I to present -browse surfaces of APCs with TCRs looking for match -if found, activate and become effector cytotoxic T cells (great for virus-infected cells, tumor cells)
62
Once activated, Helper T cells produce cytokines to activate:
B cells, Cytotoxic T cells, macrophages, etc. | -changes behavior and response of immune system
63
Antigen Presenting Cells include:
- monocytes - macrophages - dendritic cells
64
Cluster of Differentiation
defined subset of cellular surface receptors that ID cell type and stage of differentiation, and which are recognized by antibodies
65
What is the difference between the activation of NK cells and CD8+ cells?
- CD8+ cells browse APCs for antigen to match their antigen receptors - NK cells attack cells that do not display MHC I receptors. Do NOT have antigen-specific receptors
66
Function of Osteoblasts
generate bone and control HSC differentiation
67
Function of Endothelial cells
line blood vessels and regulate HSC differentiation
68
Function of sympathetic neurons
control release of cells from bone marrow
69
Where does entry of naive double negative thymocytes occur?
CMJ
70
Where do double negative thymocytes proliferate and generate TCRs, CD4, and CD8?
subscapular cortex
71
Where are double positive thymocytes tested for their ability to bind MHC complexes via cTECs? (Positive selection)
cortex
72
Double positive thymocytes are tested for their ability to bind MHC cocmplexes via
cTECs
73
Single positive thymoctyes are tested for their ability to bind proteins found in other organ types via mTECs in the
medulla
74
Single positive thymocytes are tested for their ability to bind proteins found in other organ types via
mTECs
75
Lymphoid follicles
organized microenvironments that are responsible for the development and selection of B cells that produce high-affinity antibodies
76
In a lymph node, where are B cells located?
cortex
77
In a lymph node, where are T cells located?
paracortex
78
In a lymph node, where do lymphocytes exit and plasma cells make antibodies to enter circulation?
medulla