The Journal of Experimental Medicine · 2005 · 181 citations · 38 references
Life SciencesCell BiologyImmunologyCell ProliferationDevelopmental Cell BiologyDevelopmental ImmunologyB Cell BiologyB Cell DevelopmentHumoral ImmunityImmune Cell Lineage CommitmentLymphocyte ActivationLymphocyte DevelopmentB Lymphocyte DevelopmentEarly B Cell DevelopmentFollicular B CellsMarginal Zone B Cell DevelopmentMarginal Zone B CellsPeripheral Immune Cell MaturationSteady-state Kinetics
Selection of recently formed B cells into the follicular or marginal zone (MZ) compartments is proposed to occur by way of proliferative intermediates expressing high levels of CD21/35 and CD23. However, we show that CD21/35(high) CD23(+) splenocytes are not enriched for proliferative cells, and do not contribute substantially to the generation of follicular B cells. Instead, ontogenic relationships, steady-state labeling kinetics, and adoptive transfer experiments suggest that CD21/35(high) CD23(+) splenocytes serve primarily as precursors for MZ B cells, although their developmental potential seems to be broader and is influenced by environmental cues that are associated with lymphopenia. Furthermore, CD21/35(high) CD23(+) splenocytes share several key functional characteristics with MZ B cells, including their capacity to trap T-independent antigen and a heightened proliferative response to LPS. These observations challenge previous models of peripheral B cell maturation, and suggest that MZ B cells develop by way of CD21/35(high) CD23(+) intermediates.
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By Florienne Loder, Bettina Mutschler, Robert J. Ray et al. · The Journal of Experimental Medicine · 1999 · 843 citations · Full text
Defective B cell development and function in Btk-deficient mice
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