BTLA公司
蛋白质酪氨酸磷酸酶
细胞毒性T细胞
T淋巴细胞
抗原
酪氨酸磷酸化
免疫学
抗体
受体
免疫系统
生物
分子生物学
生物化学
体外
作者
Norihiko Watanabe,Maya Gavrieli,John R. Šedý,Jianfei Yang,Francesca Fallarino,Susan K. Loftin,Michelle A. Hurchla,Natalie Zimmerman,Julia Sim,Xingxing Zang,Theresa L. Murphy,John H. Russell,James P. Allison,Kenneth M. Murphy
摘要
During activation, T cells express receptors for receiving positive and negative costimulatory signals. Here we identify the B and T lymphocyte attenuator (BTLA), an immunoglobulin domain-containing glycoprotein with two immunoreceptor tyrosine-based inhibitory motifs. BTLA is not expressed by naive T cells, but it is induced during activation and remains expressed on T helper type 1 (T(H)1) but not T(H)2 cells. Crosslinking BTLA with antigen receptors induces its tyrosine phosphorylation and association with the Src homology domain 2 (SH2)-containing protein tyrosine phosphatases SHP-1 and SHP-2, and attenuates production of interleukin 2 (IL-2). BTLA-deficient T cells show increased proliferation, and BTLA-deficient mice have increased specific antibody responses and enhanced sensitivity to experimental autoimmune encephalomyelitis. B7x, a peripheral homolog of B7, is a ligand of BTLA. Thus, BTLA is a third inhibitory receptor on T lymphocytes with similarities to cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) and programmed death 1 (PD-1).
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