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在T淋巴细胞发育过程中,前TCRα和TCRα不是TCRβ可互换的伙伴。

Pre-TCRalpha and TCRalpha are not interchangeable partners of TCRbeta during T lymphocyte development.

作者信息

Borowski Christine, Li Xiaoyan, Aifantis Iannis, Gounari Fotini, von Boehmer Harald

机构信息

Department of Pathology, Harvard Medical School, Dana-Farber Cancer Institute, Smith Building, 1 Jimmy Fund Way, Boston, MA 02115, USA.

出版信息

J Exp Med. 2004 Mar 1;199(5):607-15. doi: 10.1084/jem.20031973.

Abstract

In contrast with the alphabeta T cell receptor (TCR), the pre-TCR spontaneously segregates to membrane rafts from where it signals in a cell-autonomous fashion. The disparate behaviors of these two receptors may stem either from differences inherent to the distinct developmental stages during which they are expressed, or from features intrinsic and unique to the receptor components themselves. Here, we express TCRalpha precisely at the pre-TCR checkpoint, at levels resembling those of endogenous pre-TCRalpha (pTalpha), and in the absence of endogenous pTalpha. Both in isolation and more dramatically when in competition with pTalpha, TCRalpha induced defective proliferation, survival, and differentiation of alphabeta T lymphocyte precursors, as well as impaired commitment to the alphabeta T lymphocyte lineage. Substitution of TCRalpha transmembrane and cytoplasmic domains with those of pTalpha generated a hybrid molecule possessing enhanced competitive abilities. We conclude that features intrinsic to the pre-TCR, which are absent in TCRalpha, are essential for its unique function.

摘要

与αβ T细胞受体(TCR)不同,前TCR会自发地聚集到膜筏上,并从那里以细胞自主的方式发出信号。这两种受体的不同行为可能源于它们表达时所处不同发育阶段所固有的差异,或者源于受体组件本身内在且独特的特征。在这里,我们恰好在前TCR检查点表达TCRα,其水平与内源性前TCRα(pTα)相似,且不存在内源性pTα。单独表达时以及与pTα竞争时更显著地,TCRα诱导αβ T淋巴细胞前体的增殖、存活和分化出现缺陷,以及对αβ T淋巴细胞谱系的定向受损。用pTα的跨膜和胞质结构域替换TCRα产生了一种具有增强竞争能力的杂合分子。我们得出结论,前TCR所具有而TCRα所没有的内在特征对于其独特功能至关重要。

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