Xu S, Tan J E, Wong E P, Manickam A, Ponniah S, Lam K P
Institute of Molecular and Cell Biology, National University of Singapore, 30 Medical Drive, Singapore 117609, Republic of Singapore.
Int Immunol. 2000 Mar;12(3):397-404. doi: 10.1093/intimm/12.3.397.
Engagement of the B cell receptor (BCR) leads to the activation of tyrosine kinases and other signaling molecules that ultimately determine the type and magnitude of the B lymphocyte's cellular response. The adaptor protein BLNK/SLP-65 plays a pivotal role in BCR signal transduction by coupling Syk activation to downstream elements such as Grb2, phospholipase C-gamma, Vav and Nck. We have generated BLNK(-/-) mice to determine the physiological role of this protein in B cell development and activation. BLNK(-/-) mice exhibit an incomplete block in B cell development with a severe inhibition of pro-B to pre-B cell differentiation. BLNK(-/-) sIgM(+) cells can develop, seed the peripheral lymphoid tissues and accumulate in numbers overtime. However, these mutant B cells failed to mature and are non-responsive to BCR cross-linking in terms of proliferation and up-regulation of activation markers such as CD69 and CD86 (B7-2). In addition, the CD5(+) subset of B cells is absent. The immune response to T cell-independent antigen but not T cell-dependent antigen is also impaired. Overall, the phenotype of BLNK(-/-) mice bears a striking resemblance to that of xid mice which is the murine model of human XLA that has a mutation in Bruton's tyrosine kinase. This raises the interesting possibility that mutation in BLNK/SLP-65 may be responsible for certain human immunodeficiencies.
B细胞受体(BCR)的激活会导致酪氨酸激酶和其他信号分子的活化,这些分子最终决定B淋巴细胞细胞反应的类型和强度。衔接蛋白BLNK/SLP-65在BCR信号转导中起着关键作用,它将Syk的激活与下游元件如Grb2、磷脂酶C-γ、Vav和Nck偶联起来。我们构建了BLNK基因敲除(-/-)小鼠,以确定该蛋白在B细胞发育和激活中的生理作用。BLNK基因敲除小鼠在B细胞发育过程中表现出不完全阻断,前B细胞向pre-B细胞的分化受到严重抑制。BLNK基因敲除的表面免疫球蛋白M(sIgM)阳性细胞能够发育,定植于外周淋巴组织,并随时间积累增多。然而,这些突变的B细胞未能成熟,在增殖以及激活标志物如CD69和CD86(B7-2)上调方面对BCR交联无反应。此外,B细胞的CD5阳性亚群缺失。对非T细胞依赖性抗原而非T细胞依赖性抗原的免疫反应也受损。总体而言,BLNK基因敲除小鼠的表型与xid小鼠极为相似,xid小鼠是人类X连锁无丙种球蛋白血症(XLA)的小鼠模型,其布鲁顿酪氨酸激酶存在突变。这就引发了一个有趣的可能性,即BLNK/SLP-65的突变可能导致某些人类免疫缺陷。