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T细胞受体(TCR)通过两种不同机制诱导未成熟CD4+CD8+胸腺细胞死亡,这两种机制对CD28共刺激的需求不同:对胸腺中阴性选择的影响

T cell receptor (TCR)-induced death of immature CD4+CD8+ thymocytes by two distinct mechanisms differing in their requirement for CD28 costimulation: implications for negative selection in the thymus.

作者信息

Punt J A, Havran W, Abe R, Sarin A, Singer A

机构信息

Experimental Immunology Branch, National Cancer Institute, Bethesda, Maryland 20892, USA.

出版信息

J Exp Med. 1997 Dec 1;186(11):1911-22. doi: 10.1084/jem.186.11.1911.

Abstract

Negative selection is the process by which the developing lymphocyte receptor repertoire rids itself of autoreactive specificities. One mechanism of negative selection in developing T cells is the induction of apoptosis in immature CD4+CD8+ (DP) thymocytes, referred to as clonal deletion. Clonal deletion is necessarily T cell receptor (TCR) specific, but TCR signals alone are not lethal to purified DP thymocytes. Here, we identify two distinct mechanisms by which TCR-specific death of DP thymocytes can be induced. One mechanism requires simultaneous TCR and costimulatory signals initiated by CD28. The other mechanism is initiated by TCR signals in the absence of simultaneous costimulatory signals and is mediated by subsequent interaction with antigen-presenting cells. We propose that these mechanisms represent two distinct clonal deletion strategies that are differentially implemented during development depending on whether immature thymocytes encounter antigen in the thymic cortex or thymic medulla.

摘要

阴性选择是发育中的淋巴细胞受体库去除自身自身反应性特异性的过程。发育中T细胞阴性选择的一种机制是在未成熟的CD4+CD8+(双阳性,DP)胸腺细胞中诱导凋亡,这被称为克隆清除。克隆清除必然是T细胞受体(TCR)特异性的,但仅TCR信号对纯化的DP胸腺细胞并不致命。在此,我们确定了两种可诱导DP胸腺细胞TCR特异性死亡的不同机制。一种机制需要由CD28启动的同时存在的TCR和共刺激信号。另一种机制在没有同时存在的共刺激信号的情况下由TCR信号启动,并由随后与抗原呈递细胞的相互作用介导。我们提出,这些机制代表了两种不同的克隆清除策略,在发育过程中根据未成熟胸腺细胞是在胸腺皮质还是胸腺髓质中遇到抗原而有差异地实施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc26/2199155/76182f969d48/JEM.971308f1a.jpg

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