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Publication : Mimicry of pre-B cell receptor signaling by activation of the tyrosine kinase Blk.

First Author  Tretter T Year  2003
Journal  J Exp Med Volume  198
Issue  12 Pages  1863-73
PubMed ID  14662906 Mgi Jnum  J:87194
Mgi Id  MGI:2683860 Doi  10.1084/jem.20030729
Citation  Tretter T, et al. (2003) Mimicry of pre-B cell receptor signaling by activation of the tyrosine kinase Blk. J Exp Med 198(12):1863-73
abstractText  During B lymphoid ontogeny, assembly of the pre-B cell receptor (BCR) is a principal developmental checkpoint at which several Src-related kinases may play redundant roles. Here the Src-related kinase Blk is shown to effect functions associated with the pre-BCR. B lymphoid expression of an active Blk mutant caused proliferation of B progenitor cells and enhanced responsiveness of these cells to interleukin 7. In mice lacking a functional pre-BCR, active Blk supported maturation beyond the pro-B cell stage, suppressed VH to DJH rearrangement, relieved selection for productive heavy chain rearrangement, and stimulated kappa rearrangement. These alterations were accompanied by tyrosine phosphorylation of immunoglobulin beta and Syk, as well as changes in gene expression consistent with developmental maturation. Thus, sustained activation of Blk induces responses normally associated with the pre-BCR.
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