首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Lymphocyte inhibitor of TRAIL (TNF-related apoptosis-inducing ligand): a new receptor protecting lymphocytes from the death ligand TRAIL.
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Lymphocyte inhibitor of TRAIL (TNF-related apoptosis-inducing ligand): a new receptor protecting lymphocytes from the death ligand TRAIL.

机译:TRAIL的淋巴细胞抑制剂(TNF相关的凋亡诱导配体):一种保护淋巴细胞免受死亡配体TRAIL影响的新受体。

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摘要

Apoptosis can be triggered by the engagement of cell surface receptors by their ligands. A growing number of receptors belonging to the TNF receptor family have been identified that contain a conserved cytoplasmic death domain. These include Fas, TNF-R1, lymphocyte-associated receptor of death (LARD), DR4, and TNF-related apoptosis-inducing ligand receptor inducer of cell killing-2 (TRICK2). The latter two are receptors for the cytotoxic ligand TNF-related apoptosis-inducing ligand (TRAIL), and one of the paradoxes raised by the cloning of these molecules was why do most cells not die upon contact with the widely expressed TRAIL molecule? This is a particular problem for lymphocytes that express DR4 and TRICK2 and are in constant circulation through TRAIL-expressing tissues. We have cloned LIT (lymphocyte inhibitor of TRAIL), which lacks a death domain. LIT is expressed predominantly on PBL, where it can competitively inhibit TRAIL-induced apoptosis through DR4/TRICK2, and may function to modulate lymphocyte sensitivity to TRAIL.
机译:细胞表面受体与其配体的结合可触发细胞凋亡。已经鉴定出越来越多的属于TNF受体家族的受体,其包含保守的细胞质死亡结构域。这些包括Fas,TNF-R1,淋巴细胞相关的死亡受体(LARD),DR4和TNF相关的细胞杀伤2诱导凋亡的配体受体诱导剂(TRICK2)。后两个是细胞毒性配体TNF相关凋亡诱导配体(TRAIL)的受体,而克隆这些分子引发的悖论之一就是为什么大多数细胞在与广泛表达的TRAIL分子接触时不会死亡?对于表达DR4和TRICK2并通过表达TRAIL的组织恒定循环的淋巴细胞而言,这是一个特别的问题。我们已经克隆了LIT(TRAIL的淋巴细胞抑制剂),它缺乏死亡结构域。 LIT主要在PBL上表达,它可以通过DR4 / TRICK2竞争性抑制TRAIL诱导的凋亡,并可能起调节淋巴细胞对TRAIL敏感性的作用。

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