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10.1371/journal.pone.0174661

http://scihub22266oqcxt.onion/10.1371/journal.pone.0174661
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C5367813!5367813!28346517
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suck abstract from ncbi


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pmid28346517      PLoS+One 2017 ; 12 (3): ä
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  • CD22 is required for formation of memory B cell precursors within germinal centers #MMPMID28346517
  • Chappell CP; Draves KE; Clark EA
  • PLoS One 2017[]; 12 (3): ä PMID28346517show ga
  • CD22 is a BCR co-receptor that regulates B cell signaling, proliferation and survival and is required for T cell-independent Ab responses. To investigate the role of CD22 during T cell-dependent (TD) Ab responses and memory B cell formation, we analyzed Ag-specific B cell responses generated by wild-type (WT) or CD22-/- B cells following immunization with a TD Ag. CD22-/- B cells mounted normal early Ab responses yet failed to generate either memory B cells or long-lived plasma cells, whereas WT B cells formed both populations. Surprisingly, B cell expansion and germinal center (GC) differentiation were comparable between WT and CD22-/- B cells. CD22-/- B cells, however, were significantly less capable of generating a population of CXCR4hiCD38hi GC B cells, which we propose represent memory B cell precursors within GCs. These results demonstrate a novel role for CD22 during TD humoral responses evident during primary GC formation and underscore that CD22 functions not only during B cell maturation but also during responses to both TD and T cell-independent antigens.
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