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趋化因子RANTES对双T细胞信号通路的激活作用。

Activation of dual T cell signaling pathways by the chemokine RANTES.

作者信息

Bacon K B, Premack B A, Gardner P, Schall T J

机构信息

Department of Immunology, DNAX Research Institute of Molecular and Cellular Biology, Palo Alto, CA 94304, USA.

出版信息

Science. 1995 Sep 22;269(5231):1727-30. doi: 10.1126/science.7569902.

Abstract

The chemokine RANTES induced biphasic mobilization of Ca2+ in T cells. The initial peak, a transient increase in cytosolic Ca2+ mediated by a heterotrimeric guanine nucleotide-binding protein (G protein)--coupled pathway, was associated predominantly with chemotaxis. The second peak, Ca2+ release and sustained influx dependent on protein tyrosine kinases, was associated with a spectrum of cellular responses--Ca2+ channel opening, interleukin-2 receptor expression, cytokine release, and T cell proliferation--characteristic of T cell receptor activation. Other chemokines did not produce these responses. Thus, in addition to inducing chemotaxis, RANTES can act as an antigen-independent activator of T cells in vitro.

摘要

趋化因子RANTES可诱导T细胞内Ca2+发生双相性动员。最初的峰值,即由异三聚体鸟嘌呤核苷酸结合蛋白(G蛋白)偶联途径介导的胞质Ca2+的短暂升高,主要与趋化作用相关。第二个峰值,即依赖蛋白酪氨酸激酶的Ca2+释放和持续内流,与一系列细胞反应相关——Ca2+通道开放、白细胞介素-2受体表达、细胞因子释放以及T细胞增殖——这些都是T细胞受体激活的特征。其他趋化因子不会产生这些反应。因此,除了诱导趋化作用外,RANTES在体外还可作为T细胞的抗原非依赖性激活剂。

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