Rodriguez Rosie, Matsuda Miho, Storey Amy, Katan Matilda
Cancer Research UK Centre for Cell and Molecular Biology, Chester Beatty Laboratories, The Institute of Cancer Research, Fulham Road, London SW3 6JB, UK.
Biochem J. 2003 Aug 15;374(Pt 1):269-80. doi: 10.1042/BJ20021778.
Studies of PLCgamma (phospholipase Cgamma) have identified a number of regulatory components required for signalling; however, molecular mechanisms and the relationship between events leading to translocation and an increase of substrate hydrolysis have not been well defined. The addition of a membrane-targeting tag to many signal transducers results in constitutive activation, suggesting that these processes could be closely linked and difficult to dissect. The present study of PLCgamma2 regulation by cross-linking of the BCR (B-cell antigen receptor) or H2O2 stress in DT40 B-cells, demonstrated that the membrane targeting is a separate step from further changes that result in enzyme activation and substrate hydrolysis. Furthermore, we have defined the roles of different domains of PLCgamma2 and, using a panel of cell lines deficient in components linked to PLCgamma2 regulation, the involvement of signalling molecules with respect to each of the steps. We have found that only the lipid-raft-targeted Lyn-PLCgamma2 construct, unlike non-specific membrane targeting, overcame the requirement for the adapter protein BLNK (B-cell linker). The stable expression of Lyn-PLCgamma2 was not accompanied by an increase in substrate hydrolysis in resting cells, which followed stimulation and specifically required the presence and/or activation of Syk, Btk, phosphoinositide 3-kinase but not BLNK, as established using deficient cell lines or specific inhibitors. Based on mutational analysis of the specific tyrosine residues [Tyr753-->Phe (Y753F)/Y759F] and SH2 (Src homology 2) domains (R564A/R672A) in the context of Lyn-PLCgamma2, we found that Tyr753/Tyr759 were essential, whereas the PLCgamma2 SH2 domains did not have an important role in the transient activation of Lyn-PLCgamma2 but may serve to stabilize an activated form in sustained activation.
对磷脂酶Cγ(PLCγ)的研究已确定了信号传导所需的多种调节成分;然而,分子机制以及导致转位和底物水解增加的事件之间的关系尚未明确界定。在许多信号转导器上添加膜靶向标签会导致组成型激活,这表明这些过程可能紧密相连且难以剖析。本研究通过在DT40 B细胞中交联B细胞抗原受体(BCR)或施加H2O2应激来研究PLCγ2的调节,结果表明膜靶向是一个与导致酶激活和底物水解的进一步变化分开的步骤。此外,我们确定了PLCγ2不同结构域的作用,并利用一组缺乏与PLCγ2调节相关成分的细胞系,研究了信号分子在每个步骤中的参与情况。我们发现,与非特异性膜靶向不同,只有脂质筏靶向的Lyn-PLCγ2构建体克服了对接蛋白BLNK(B细胞连接蛋白)的需求。Lyn-PLCγ2的稳定表达在静息细胞中并未伴随底物水解增加,静息细胞在受到刺激后,底物水解增加特别需要Syk、Btk、磷酸肌醇3激酶的存在和/或激活,但不需要BLNK,这是通过使用缺陷细胞系或特异性抑制剂确定的。基于在Lyn-PLCγ2背景下对特定酪氨酸残基[Tyr753→Phe(Y753F)/Y759F]和Src同源2(SH2)结构域(R564A/R672A)的突变分析,我们发现Tyr753/Tyr759至关重要,而PLCγ2的SH2结构域在Lyn-PLCγ2的瞬时激活中没有重要作用,但可能在持续激活中起到稳定激活形式的作用。