Huang Guo N, Huso David L, Bouyain Samuel, Tu Jianchen, McCorkell Kelly A, May Michael J, Zhu Yuwen, Lutz Michael, Collins Samuel, Dehoff Marlin, Kang Shin, Whartenby Katharine, Powell Jonathan, Leahy Daniel, Worley Paul F
Program in Biochemistry, Cellular and Molecular Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Science. 2008 Jan 25;319(5862):476-81. doi: 10.1126/science.1151227.
T cell receptor (TCR) and costimulatory receptor (CD28) signals cooperate in activating T cells, although understanding of how these pathways are themselves regulated is incomplete. We found that Homer2 and Homer3, members of the Homer family of cytoplasmic scaffolding proteins, are negative regulators of T cell activation. This is achieved through binding of nuclear factor of activated T cells (NFAT) and by competing with calcineurin. Homer-NFAT binding was also antagonized by active serine-threonine kinase AKT, thereby enhancing TCR signaling via calcineurin-dependent dephosphorylation of NFAT. This corresponded with changes in cytokine expression and an increase in effector-memory T cell populations in Homer-deficient mice, which also developed autoimmune-like pathology. These results demonstrate a further means by which costimulatory signals are regulated to control self-reactivity.
T细胞受体(TCR)和共刺激受体(CD28)信号协同激活T细胞,尽管对这些信号通路自身如何被调控的理解还不完整。我们发现,Homer家族的细胞质支架蛋白成员Homer2和Homer3是T细胞激活的负调控因子。这是通过结合活化T细胞核因子(NFAT)并与钙调磷酸酶竞争来实现的。活性丝氨酸 - 苏氨酸激酶AKT也拮抗Homer - NFAT结合,从而通过NFAT的钙调磷酸酶依赖性去磷酸化增强TCR信号传导。这与细胞因子表达的变化以及Homer缺陷小鼠中效应记忆T细胞群体的增加相对应,这些小鼠还出现了自身免疫样病理。这些结果证明了一种进一步调控共刺激信号以控制自身反应性的方式。