da Silva A J, Li Z, de Vera C, Canto E, Findell P, Rudd C E
Division of Tumor Immunology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA 02115, USA.
Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7493-8. doi: 10.1073/pnas.94.14.7493.
T cell receptor zeta (TcRzeta)/CD3 ligation initiates a signaling cascade that involves src kinases p56(lck) and zeta-associated protein 70, leading to the phosphorylation of substrates such as TcRzeta, Vav, SH2-domain-containing leukocyte protein 76 (SLP-76), cbl, and p120/130. FYN binding protein (FYB or p120/130) associates with p59(fyn), the TcRzeta/CD3 complex, and becomes tyrosine-phosphorylated in response to receptor ligation. In this study, we report the cDNA cloning of human and murine FYB and show that it is restricted in expression to T cells and myeloid cells and possesses an overall unique hydrophilic sequence with several tyrosine-based motifs, proline-based type I and type II SH3 domain binding motifs, several putative lysine/glutamic acid-rich nuclear localization motifs, and a SH3-like domain. In addition to binding the src kinase p59(fyn), FYB binds specifically to the hematopoietic signaling protein SLP-76, an interaction mediated by the SLP-76 SH2 domain. In keeping with this, expression of FYB augmented interleukin 2 secretion from a T cell hybridoma, DC27.10, in response to TcRzeta/CD3 ligation. FYB is therefore a novel hematopoietic protein that acts as a component of the FYN and SLP-76 signaling cascades in T cells.
T细胞受体ζ链(TcRζ)/CD3连接引发了一个信号级联反应,该反应涉及src激酶p56(lck)和ζ相关蛋白70,导致诸如TcRζ、Vav、含SH2结构域的白细胞蛋白76(SLP-76)、cbl和p120/130等底物的磷酸化。FYN结合蛋白(FYB或p120/130)与p59(fyn)、TcRζ/CD3复合物结合,并在受体连接时发生酪氨酸磷酸化。在本研究中,我们报道了人和小鼠FYB的cDNA克隆,并表明其表达仅限于T细胞和髓样细胞,具有整体独特的亲水序列,带有几个基于酪氨酸的基序、基于脯氨酸的I型和II型SH3结构域结合基序、几个推定的富含赖氨酸/谷氨酸的核定位基序以及一个类SH3结构域。除了结合src激酶p59(fyn)外,FYB还特异性地结合造血信号蛋白SLP-76,这种相互作用由SLP-76的SH2结构域介导。与此一致的是,FYB的表达增强了T细胞杂交瘤DC27.10在TcRζ/CD3连接时白细胞介素2的分泌。因此,FYB是一种新型造血蛋白,在T细胞中作为FYN和SLP-76信号级联反应的一个组成部分发挥作用。