Lec 16: B cell DADM Flashcards

1
Q

VDJ recombhination

A

process by which T cells and B cells randomly assemble different gene segements
variable V, diversity D, and joining J regions

generates unqiue receptors (known as antigen receptors) that can collectively recognize many different types of molecuels

requries the activity of RAG1/2 compelx

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2
Q

consider VDJ recombination of light and heavy chains

A

bruh idk

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3
Q

multiple gene segements

A

VDJ segment recombination provides extensive combinatoral diveristy

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4
Q

P nucleotide addition

A

adds a short palindromic sequence at the join

allows for the coding of more peptides

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5
Q

Exonuclease trimming

A

loss of nucleotides at the joints

loss of aa = end up with a different sequence

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6
Q

non-tempalte N nucleotide additon

A

facilitated by TdT enzyme, up to 20 extra nuclotides can be added at the joints of heavby chain genes

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7
Q

combinatoral diversity

A

same heavy chain can combine with different light chains and vise versa

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8
Q

somatic hyper mutation

A

through the activity of an enzyme called activation induced (cytidine) deaminse (AID) and DNA repair process, the variable regions of IG-BcR locus ar emutated

lots leads to frameshift mutations, and thus the loss of a functional BcR

However can lead to new affinity/ a higher affinity for something you otherwise couldn’t code for

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9
Q

Class-switch recombination

A

CSR

process by which immunoglobulin heaavy chain locus contant region is changed, but the variable region remains the same (this is also called isotype swithing)

  • > does not alter antigen specificity
  • > central to the maturation of the antibody resposne
  • > crucially requires cyidine deaminase AID
  • > is an irreverible process
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10
Q

B cell development and clonal selection

A

clonal selection hypthesis:

each B cell bears a singal type fo BcR

*Upon stimulation, each cell will create a clone of cells bearing the same Ag receptor as the original

activated B cells can become antibody secreting plasma cells or memoty B cells

memory cells retain thier BcR, howver plasma lose them and secrete them instead

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11
Q

B cell antigen recognition

bcr clustering induces internalization and antigen presentation by b cell

A

Inital interactions induce a clustering of bcr and ther cognate antigens

  • > antigen binding induces conformational change in cu4domain -> oligomerization of antigen-bound igM moleucles
  • > antigen ahbound bcr moved into lipid rafts of the membrane -> allows for association of bcr signalling molecules -acitvation signal

bcell membrane rapidly spreads over the target membrane before contracting back
-> the entire process takes only minutes to comples

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12
Q

bcr causes smac formaiton

A

coordinated cell signalling and antigen extraction

b cells can capture membrane bound antigens from other APCs

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13
Q

T cell-depended B cell responses

classical Bcell activaion

A

B-cell bind antigen via bcr

within secondary lymphoid organs, inteaction with Th cells provides co-stimulation and cytokines for differentiation and memory cell production

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14
Q

T cell-depended B cell responses

B-cell bind antigen via bcr

A

antigen recognition by mature B cells provides a survival signal

if B cell doesn’t encounter its cogante Ag, it will die by apoptosis within moths after emerging from the bone marrow. ( tonic Bcr singlalling generaties a survival response)

inital activationa nd proliferation events

some antigen is internalised, processed and presented on MHCII
-> exogenous antigen (needs to be internalized and processes)***

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15
Q

T cell-depended B cell responses

within secondary lymphoid organs, inteaction with Th cells provides co-stimulation and cytokines for differentiation and memory cell production

A

B celles express CCR7 after antigen processing

B cells move into T cell rich zone until they encounter and interact with theri counterpart antigen-specific T cell

Bcells then down-regulate CCR7, leave Tcell areas and enter follicles
->innitial for mation of a GC
-> internalization and prossecing of antigen
=many different peptides
=many Th cells could activate the Bcells
=many novel peptides processed and presented on MHCII
-> many different T cells could recognize

BcR and TcR dont recognize the same thing

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16
Q

B cell differentation and memory

A

plasma cells are Ig producting machines

  • > found within the first 5-6 days of immune responses in lymph
  • > some stay in GCs and lymph nodes, others home back to the bonemarrow

Class-switched memory B cells have primarily a plasma cell fate

Other activated B cells (IgM+IdG+) move into the follicles and initatite a GC response

17
Q

activated B cells (IgM+IdG+) move into the follicles and initatite a GC response

A

CD40/CD40L costimulation between B/T cells and cytokines form FDCs and Tfh cells stimulate proliferation further

follidle dark zone = densly pakced with proligerating B cells

Follicle light zone = B cells intersparesed within the FDC network

18
Q

Collapse of antigen-specific B cell population

A

most B cells are lost at the ends of the primary immune response
-> lack of antigen means reduciton in survival signals-> apoptosis mechanism via Fas-FasL

Remaing memory cells

  • > respond to lower concentration of antigens
  • > faster response to antigen stimulation
  • > higher-affinity ig receptors
  • > class switched IgD-
  • > longer lived cells
19
Q

T-depended responses require help from T cells

TD

A

TD-1: Recognition of protein Ag+ Tfh helo

TD-2: Tecognition of lipid Ag+ NKTfh helo

convential T cell dependent B cell responses are optimal for producing memory plasma cells
-> long term immunity

20
Q

T-independent responses do not require T-cell help

TI

A

TI-1: Ag binds B cells via PRRs and BcR

TI-2: Elicited by distinct Ag types whihc cross-link large numbers of BcRs

TI-3: B cells receive help from bone-marrow derived myeloid cells

21
Q

Two subclasses of B cells mediate the response to T-independent antigens

A

B-1 and marginal zone B cells

22
Q

B-1 cells

A

Polyspecific antibodies (broad and low affinity)= innate and adaptive

  • > often recognize polysaccharides antigens
  • > clustering of antigen (in large immune complexes) facillitaes antigen internalizationa and prevention of microbial disseminaiton

CD5+, and 5% of Bcell population, primarily produce IgM

self-renewing in the periphery, moslty in the peritoneal and pleural cavities

do not develop into memory cells

like gd T cells, functional niche bridges innate and adaptive immunity

23
Q

Marginal zone B cells

A

Must receive low-level signals through bcR for Survival

self-renewing in the periphery

specilized to respond to blood-borne antigen entering the spleen

24
Q

High-affinity requires T cells

A

Dual BcR and TLR engagement also generates high-affinity and class-swithced B cells

class switch recombination can occur independent of T cell help however, somatic hypermutation requires T cell help

25
Q

What is the function of RAG1/2

A

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26
Q

What is the funciton of TdT

A

Terminal deoxynucleotidyl transferase (TdT), also known as DNA nucleotidylexotransferase (DNTT) or terminal transferase, is a specialized DNA polymerase expressed in immature, pre-B, pre-T lymphoid cells, and acute lymphoblastic leukemia/lymphoma cells. TdT adds N-nucleotides to the V, D, and J exons of the TCR and BCR genes during antibody gene recombination,

27
Q

What is the function of AID

A

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28
Q

What is VDJ recombination and how doe sit impact formation of the bcr

A

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29
Q

What is class switch recombination and how does it impact antbody production

A

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30
Q

List the steps of GC formation

A

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31
Q

Compare and contrast T cell dependent and T cell independent B cell activation

A

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