Distinct signals mediate maturation and allelic exclusion in lymphocyte progenitors

被引:80
作者
Iritani, BM
Alberola-Ila, J
Forbush, KA
Perlmutter, RM [1 ]
机构
[1] Univ Washington, Howard Hughes Med Inst, Dept Immunol, Seattle, WA 98195 USA
[2] Univ Washington, Howard Hughes Med Inst, Dept Biochem, Seattle, WA 98195 USA
[3] Univ Washington, Howard Hughes Med Inst, Dept Med Med Genet, Seattle, WA 98195 USA
[4] Univ Washington, Howard Hughes Med Inst, Dept Comparat Med, Seattle, WA 98195 USA
[5] CALTECH, Div Biol, Pasadena, CA 92115 USA
[6] Merck Res Labs, Rahway, NJ 07065 USA
关键词
D O I
10.1016/S1074-7613(00)80070-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Successful in-frame rearrangement of immunoglobulin heavy chain genes or T cell antigen receptor (TCR) beta chain genes in lymphocyte progenitors results in formation of pre-BCR and pre-TCR complexes. These complexes signal progenitor cells to mature, expand in cell number, and suppress further rearrangements at the immunoglobulin heavy chain or TCR beta chain loci, thereby ensuring allelic exclusion. We used transgenic expression of a constitutively active form of c-Raf-1 (Raf-CAAX) to demonstrate that activation of the Map kinase pathway can stimulate both maturation and expansion of B and T lymphocytes, even in the absence of pre-TCR or pre-BCR formation. However, the same Raf signal did not mediate allelic exclusion. We conclude that maturation of lymphocyte progenitors and allelic exclusion require distinct signals.
引用
收藏
页码:713 / 722
页数:10
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