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L8 - B cell development

Jack Rowe I&I. Year 2 Inglés 54 fichas

L8 - B cell development

Fichas del conjunto (54)

  1. 1what is the purpose of the effector section of the antibodyallows interaction with compliment or other molecules
  2. 2clinically why are effecter regions of the B cell useful?we can attach drugs or target things to the effector section of the antibody
  3. 3how do we know that antibodies are a really important aspect of the immune syste,diseases which decrease the number/ effectiveness of antibodies are very severe
  4. 4why are huge deficiencies in antibody numbers very rare?- because this will kill people off v quickly
    - meaning any congenital issue like this would be removed from the gene pool before reproductive age
  5. 5what 2 main receptors are found on B cells which bind to antigen?- the B cell receptor
    - the immunoglobulin itself
  6. 6what 2 cell types can B cells differentiate into?plasma cells and memory B cells
  7. 7what is the purpose of B cells havingMHC2 receptors on their membranes?allows the B cell to activate CD4+ T helper cells which will aid in the B cell maturation
  8. 8give a few important mechanisms used ny antibody which aid the immune syste,- binds to bacterial toxins
    - labelling the surface of pathogens for destruction by macrophages etc
    - compliment activation
  9. 9where are B cells first made and then whre are they made in adults?- first made in foetal livers
    - then made ion Bone marrow
  10. 10where does the majority of B cell development happen?in the bone marrow
  11. 11what are the 3 main types of B cellls (not differentiated cell)- B1 B cells
    - Follicular B cells
    - Marginal Zone antibodies
  12. 12why does B cell activity need to be highly regulated?to prevent autoimmunity and cancer
  13. 13give the life cycle of a B cell- B stem cell in bone marrow proliferates and differentiates into Naive B cell
    - B cell binds to complimentry antigen to activate it
    - differentiates into plasma or memory B cell
  14. 14what is the first step in production of. B cell in the bone marrow?B cell precursor rearranges its immunoglobulin genes randomly to give a random receptor
  15. 15how is autoimmunity prevented in B cell development in the bone marrowq?- negative selection
    - host cell antigens are presented to the B cell receptors, if they bind then the B cell is killed off
  16. 16where does negative selection happen for a B cell?in the bone marrow
  17. 17what chain of the B cell receptor is made first?the heavy chain
  18. 18specifically which receptor genes are rearranged during heavy chain development?D-J and V-DJ genes
  19. 19is the light chain formed by the time the heavy chain is presented on the cell surface?no
    - makes heavy chain which is presented on a surrogate light chain to the surface... then goes to make the light chain
  20. 20specifically which light chain genes are rearranged during receptor developmentV-J genes
  21. 21what happens to the light chain once its been formed?its incorporated into the heavy chain to make a complete BCR
  22. 22what 2 antibodies are present on the first mature B cellIGM and IGD
  23. 23once both heavy and light chains are formed what happens to gene rearangementits stopped
  24. 24what is the success rate of BCR gene rearangement?70% failure rate per chain recombination
  25. 25how does the B cell prevent further gene rearrangement after the BCR is formed?preventing RAG expression and function
    (RAG is gene responsible for rearrangement)
  26. 26are both inherited chromosomes recombined for BCR's?yes but one at a time
  27. 27what is the term for stopping gene rearrangement once the BCR has been formed?allelic exclusion
  28. 28what are the 2 light chains called?kappa and lambda
  29. 29what is the ratio of Kappa : Lambda in humans?2-3:1
  30. 30why does the cell use all potential genes for BCR development?raises chance of making successful BCR
  31. 31what cells in the bone marrow do B cells develop onstromal cells
  32. 32what do stromal cells do to aid B cell devlopment- give contact dependant support
    - release cytokines
  33. 33what are the 2 outcomes if a B ell recognises host cell receptors?apoptosis
    receptor rearrangement
  34. 34in B cells does positive or negative selection happen first?negative selection happens before positive selection
    (remove host targeting cells first)
  35. 35how does the B cell undergo positive selection?- if there is need for the B cell itll be given a survival signal
    - if not itll die
  36. 36which chain is rearranged in a pro B cell and which is rearranged in a pre B cel?pro-B cell = heavy chain rearrangements
    pre-B cell = light chain rearrangements
  37. 37what immunoglobulin is presented by immature B cells?IGM
  38. 38what antibodies do mature B cells present?any of the random ones + IGD
  39. 39give the difference in receptors from resting B cells and plasma cells- resting B cells: lots of MHC 2, surface antigen but not IG secretion
    - plasma cellss: have low surface IG, has no MHC2, has high rate of IG secretion
  40. 40out of resting B cells and plasma cells which can undergo somatic hypermutation and isotype switching?- only the resting B cell
    - this is why the plasma cell loses its MHC2 receptors
  41. 41why does the resting B cell have lots of surface BCR'sto increase chance of detecting pathogen antigen
  42. 42explain "Plasma cells are terminally differentiated"they cant undergo isotope switching or somatic hypermutation, they are finished maturing
  43. 43what are the 2 mechanisms of Bc ell antibody responses- T cell dependant activation
    - T cell independant activation
  44. 44explain T cell independant- no T cell driven maturation
    - some IGM and IGG but little fine tuning of the receptors to the pathogen
  45. 45explain T cell dependant antibody responserecruiting T cells allows cross talk and fine tuning of the antibdoy response
  46. 46which out of the 2 types of B cell antibody responses produced Memory B cellsT cell dependant antibody responses gives memory B cells
  47. 47what is the benefit of T cell dependant antibody responsethe antibodies are much more specific and gives a much more long lived response
  48. 48why are vaccination programs given to young children?because their T independant responses are poor
  49. 49where does T dependant antibody response begin?in germinal centres such as in lymphoid tissue and the spleen
  50. 50what are the 2 sections of germinal centres- the follicle
    - the T zone
  51. 51what are found in the follicles and the T zones of germinal centres?- T zones are just T cells
    - follicles are B cells
  52. 52give the full life cycle of a B cellgive the full life cycle of a B cell
  53. 53another helpful diagramanother helpful diagram
  54. 54—

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Descripción
Year 2 I&I. Fichas sobre L8 - B cell development, creado por Jack Rowe el 21/12/2022.
Creado por
Jack Rowe · dic 2022
Actualizado
21 dic 2022
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