Ishiai M, Sugawara H, Kurosaki M, Kurosaki T
Department of Molecular Genetics, Institute for Liver Research, Kansai Medical University, Moriguchi, Japan.
J Immunol. 1999 Aug 15;163(4):1746-9.
To explore the mechanism(s) by which phospholipase C (PLC)-gamma 2 participates in B cell Ag receptor (BCR) signaling, we have studied the function of PLC-gamma 2 mutants in B cells deficient in PLC-gamma 2. Mutation of the N-terminal Src homology 2 domain [SH2(N)] resulted in the complete loss of inositol 1,4, 5-trisphosphate generation upon BCR engagement. A possible explanation for the SH2(N) requirement was provided by findings that this mutation abrogates the association of PLC-gamma 2 with an adaptor protein BLNK. Moreover, expression of a membrane-associated form (CD16/PLC-gamma 2) with SH2(N) mutation required coligation of BCR and CD16 for inositol 1,4,5-trisphosphate generation. Together, our results suggest a central role for the SH2(N) domain in directing PLC-gamma 2 into the close proximity of BCR signaling complex by its association with BLNK, whereby PLC-gamma 2 becomes tyrosine phosphorylated and thereby activated.
为了探究磷脂酶C(PLC)-γ2参与B细胞抗原受体(BCR)信号传导的机制,我们研究了PLC-γ2突变体在缺乏PLC-γ2的B细胞中的功能。N端Src同源2结构域[SH2(N)]的突变导致BCR激活后肌醇1,4,5-三磷酸生成完全丧失。该SH2(N)需求的一种可能解释来自以下发现:此突变消除了PLC-γ2与衔接蛋白BLNK的结合。此外,具有SH2(N)突变的膜相关形式(CD16/PLC-γ2)的表达需要BCR和CD16共同结合才能生成肌醇1,4,5-三磷酸。总之,我们的结果表明SH2(N)结构域通过与BLNK结合,在将PLC-γ2引导至BCR信号复合物附近发挥核心作用,由此PLC-γ2发生酪氨酸磷酸化并被激活。