Interleukin-7 is necessary to maintain the B cell potential in common lymphoid progenitors

被引:181
作者
Dias, S [1 ]
Silva, H [1 ]
Cumano, A [1 ]
Vieira, P [1 ]
机构
[1] Inst Pasteur, INSERM, U668, Unite Dev Lymphocytes, F-75724 Paris, France
关键词
D O I
10.1084/jem.20042393
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin-7 (IL-7) promotes survival and expansion of lymphoid precursors. We show here that, in addition, IL-7 has a fundamental role, as early as the stage of the multipotent (B/T/NK) common lymphoid progenitor (CLP), in maintaining the B cell differentiation program open. CLPs generated in the absence of IL-7 have normal T/NK differentiation potential, but severely impaired B potential. Accordingly, CLPs from IL-7-deficient mice express lower amounts of early B cell factor (EBF) and Pax5 than wild-type CLPs, but similar amounts of GATA-3. Importantly, induced overexpression of EBF is sufficient to restore the B potential in these cells. These results indicate that IL-7 directs commitment of CLPs by modulating EBF expression. This is the first example of a cytokine influencing lymphoid lineage commitment in multipotent progenitors and highlights the relevance of the expression of a functional IL-7 receptor at the CLP stage.
引用
收藏
页码:971 / 979
页数:9
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