Iritani B M, Alberola-Ila J, Forbush K A, Perimutter R M
Department of Immunology, Howard Hughes Medical Institute, University of Washington, Seattle 98195, USA.
Immunity. 1999 Jun;10(6):713-22. doi: 10.1016/s1074-7613(00)80070-9.
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 TCRbeta 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.
淋巴细胞祖细胞中免疫球蛋白重链基因或T细胞抗原受体(TCR)β链基因成功进行框内重排会导致前B细胞受体(pre-BCR)和前T细胞受体(pre-TCR)复合物的形成。这些复合物向祖细胞发出信号,使其成熟、细胞数量扩增,并抑制免疫球蛋白重链或TCRβ链基因座处的进一步重排,从而确保等位基因排斥。我们利用组成型活性形式的c-Raf-1(Raf-CAAX)的转基因表达来证明,即使在没有pre-TCR或pre-BCR形成的情况下,丝裂原活化蛋白激酶(Map)途径的激活也能刺激B淋巴细胞和T淋巴细胞的成熟与扩增。然而,相同的Raf信号并未介导等位基因排斥。我们得出结论,淋巴细胞祖细胞的成熟和等位基因排斥需要不同的信号。