Koonpaew Surapong, Janssen Erin, Zhu Minghua, Zhang Weiguo
Department of Immunology, Duke University Medical Center, Durham, North Carolina 27710, USA.
J Biol Chem. 2004 Mar 19;279(12):11229-35. doi: 10.1074/jbc.M311394200. Epub 2004 Jan 13.
NTAL (non-T cell activation linker)/LAB (linker for activation of B cells) is a LAT (linker for activation of T cells)-like molecule that is expressed in B cells, mast cells, natural killer cells, and monocytes. Upon engagement of the B cell receptor or Fc receptors, it is phosphorylated and interacts with Grb2. LAB is capable of rescuing thymocyte development in LAT(-/-) mice. In this study, we utilized various LAB Tyr to Phe mutants to map the phosphorylation and Grb2-binding sites of LAB. We also examined the function of these mutants by investigating their ability to rescue signaling defects in LAT-deficient Jurkat cells and thymocyte development in LAT(-/-) mice. Our results indicated that human LAB was primarily phosphorylated on three membrane-distal tyrosines, Tyr(136), Tyr(193), and Tyr(233). Mutation of these three tyrosines abolished Grb2 binding and LAB function. Our data suggested that these tyrosines are the most important tyrosines for LAB function.
NTAL(非T细胞激活连接蛋白)/LAB(B细胞激活连接蛋白)是一种类似于LAT(T细胞激活连接蛋白)的分子,在B细胞、肥大细胞、自然杀伤细胞和单核细胞中表达。当B细胞受体或Fc受体被激活时,它会发生磷酸化并与Grb2相互作用。LAB能够挽救LAT基因敲除(-/-)小鼠的胸腺细胞发育。在本研究中,我们利用各种LAB酪氨酸突变为苯丙氨酸的突变体来确定LAB的磷酸化位点和Grb2结合位点。我们还通过研究这些突变体挽救LAT缺陷型Jurkat细胞信号缺陷和LAT基因敲除(-/-)小鼠胸腺细胞发育的能力来检测它们的功能。我们的结果表明,人LAB主要在三个远离细胞膜的酪氨酸位点Tyr(136)、Tyr(193)和Tyr(233)上发生磷酸化。这三个酪氨酸的突变消除了Grb2结合和LAB功能。我们的数据表明,这些酪氨酸是LAB功能最重要的酪氨酸。