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抗原受体介导的早期信号转导,而无需进入T细胞活化阶段。

Early signal transduction by the antigen receptor without commitment to T cell activation.

作者信息

Goldsmith M A, Weiss A

机构信息

Department of Medicine, University of California, San Francisco.

出版信息

Science. 1988 May 20;240(4855):1029-31. doi: 10.1126/science.3259335.

Abstract

The T lymphocyte antigen-receptor complex mediates antigen-specific cell activation, at least in part, through the production of inositolphospholipid-derived second messengers. Little is known about how second messenger events, typically measured within minutes of ligand binding, eventually lead to distal biologic responses such as expression of lymphokine genes. Several monoclonal antibodies directed against the receptor complex were tested for their ability to elicit transmembrane signaling in the parental Jurkat line and in a somatic mutant (J.CaM1) with a deficient receptor function. One antibody elicited substantial early Ca2+ mobilization responses in both cells but was unable to promote expression of the interleukin-2 gene in J.CaM1. In J.CaM1 there was a diminished production of phosphatidylinositol second messengers, and the elevation in intracellular free Ca2+ was transient. Thus, short-term Ca2+ mobilization does not always indicate complete signal transmission and lead to a full cellular response.

摘要

T淋巴细胞抗原受体复合物至少部分地通过产生肌醇磷脂衍生的第二信使来介导抗原特异性细胞活化。关于第二信使事件(通常在配体结合后几分钟内测量)最终如何导致诸如淋巴因子基因表达等远端生物学反应,人们了解甚少。测试了几种针对受体复合物的单克隆抗体在亲本Jurkat细胞系和受体功能缺陷的体细胞突变体(J.CaM1)中引发跨膜信号传导的能力。一种抗体在两种细胞中均引发了大量的早期Ca2+动员反应,但无法促进J.CaM1中白细胞介素-2基因的表达。在J.CaM1中,磷脂酰肌醇第二信使的产生减少,细胞内游离Ca2+的升高是短暂的。因此,短期的Ca2+动员并不总是表明信号完全传递并导致完整的细胞反应。

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