chapter 9 Flashcards

1
Q

The α and γ chain are similar in structure to the antibody ____________

A

light chain

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2
Q

The β and δ chain are similar in structure to the antibody ________________

A

heavy chain

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3
Q

What mechanisms also control whether the cell produces membrane-bound or secreted IgM?

A

mRNA splicing

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4
Q

Why does blood cell development change locations?

A

bone marrow isn’t formed right at fertilization

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5
Q

Hematopoiesis stages are defined by:

A

cell-surface markers, transcription factor expression, and Ig gene rearrangements

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6
Q

_________________in the bone marrow provide support and growth factors to developing cells

A

stromal cells

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7
Q

Describe the pre-B-cell receptor:

A

-expressed in early pre-B stage
-heavy-chain rearrangement is finalized
-Ig heavy chain complexed with VpreB and λ5 (SLC)

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8
Q

Late pre-B stage is marked by:

A

initiation of light-chain gene rearrangement, then completion

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9
Q

IgM receptor is expressed on the cell surface, transitioning the
cell into_______________

A

immature B-cell stage

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10
Q

Immature B cells in the bone marrow are exquisitely sensitive to _______________ induction.

A

tolerance

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11
Q

Immature B cells bear membrane ___________________

A

IgM, B220, CD25, IL-7R, and CD19

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12
Q

What are the three possible outcomes after surface receptors are tested against self-antigens?

A

-clonal deletion of strongly autoreactive cells
-receptor editing
-anergy

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13
Q

how does clonal deletion of strongly autoreactive cells occur?

A

-through apoptosis
-termed central tolerance as it occurs in bone marrow

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14
Q

what is receptor editing?

A

reactivation of recombination machinery

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15
Q

what is anergy?

A

induction of nonresponsiveness to further stimuli
(even self-antigen stimuli)

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16
Q

What happens to the self-reactive B cells that don’t undergo deletion?

A

Some are released to the periphery and subject to
further round of selection

17
Q

What are the two subsets of immature B cells?

A

Transitional B cells— T1 and T2

18
Q

Transitional B cells differ in gene expression as they progress through the ________________ for further maturation.

A

spleen

19
Q

The T1 subset is still undergoing screening, possessing the possibility of a ____________________ event.

A

negative selection

20
Q

Mature, primary _________B cells migrate to the lymphoid follicles.

A

B-2

21
Q

What antibodies are expressed on the surface of B-2 B cells?

A

IgM and IgD

22
Q

Describe B-2 B cells:

A

– Recirculate between blood and lymphoid organs
– Help to respond to antigens with T-cell help by
producing antibodies
– Half-life of approximately 4.5 months in periphery

23
Q

Where do B-1 B cells develop from?

A

fetal liver to protect fetus from common microbial antigens

24
Q

B-1 B cells constitute 30%-50% of B cells in what cavities of mice?

A

pleural and peritoneal

25
Q

Describe B-1 B cell receptors:

A

-tend to bind microbial carbohydrate antigens
-bind with relatively low affinity
-similar to PRRs of innate immunity

26
Q

B-1 B cells undergo apoptosis unless they interact with _______________

A

self-antigens

27
Q

where are marginal zone cells found?

A

white pulp outer regions of the spleen

28
Q

describe marginal zone cells:

A

-Appear to be specialized for blood-borne Ag recognition
-Recognize protein and carbohydrate antigens—similar to B-1
cells; Some may be able to do so without T-cell help
-Characterized by low levels of IgD and Fc receptor
-Seem to be derived from T2 cells with strong self-Ag signaling through BCR and binding of Notch ligands

29
Q

What are the characteristics shared by B and T cell developmental pathways?

A

– Rearrangement of gene segments
– Screening processes to avoid self-reactivity
– Production of small subsets with discrete functions
– Production of larger “general purpose” subsets

30
Q

What are the differences between B and T cell developmental pathways?

A

– Location of maturation and screening
– Screening processes used
* Positive and negative in T cells
* Negative in B cells
– Specific arrangements and identities of gene segments
recombined together
– Eventual outcomes of antigen receptor stimulation
* T cells require presentation and differentiate into helper or
killer subsets
* B cells require T-cell help and secrete antibodies