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一种TRAIL的拮抗剂诱饵受体和含死亡结构域的受体。

An antagonist decoy receptor and a death domain-containing receptor for TRAIL.

作者信息

Pan G, Ni J, Wei Y F, Yu G, Gentz R, Dixit V M

机构信息

Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, 48109, USA.

出版信息

Science. 1997 Aug 8;277(5327):815-8. doi: 10.1126/science.277.5327.815.

Abstract

TRAIL, also called Apo2L, is a cytotoxic protein that induces apoptosis of many transformed cell lines but not of normal tissues, even though its death domain-containing receptor, DR4, is expressed on both cell types. An antagonist decoy receptor (designated as TRID for TRAIL receptor without an intracellular domain) that may explain the resistant phenotype of normal tissues was identified. TRID is a distinct gene product with an extracellular TRAIL-binding domain and a transmembrane domain but no intracellular signaling domain. TRID transcripts were detected in many normal human tissues but not in most cancer cell lines examined. Ectopic expression of TRID protected mammalian cells from TRAIL-induced apoptosis, which is consistent with a protective role. Another death domain-containing receptor for TRAIL (designated as death receptor-5), which preferentially engaged a FLICE (caspase-8)-related death protease, was also identified.

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL),也称为Apo2L,是一种细胞毒性蛋白,可诱导多种转化细胞系凋亡,但不会诱导正常组织凋亡,尽管其含死亡结构域的受体DR4在这两种细胞类型上均有表达。已鉴定出一种拮抗剂诱饵受体(称为TRID,即无细胞内结构域的TRAIL受体),它可能解释正常组织的抗性表型。TRID是一种独特的基因产物,具有细胞外TRAIL结合结构域和跨膜结构域,但没有细胞内信号结构域。在许多正常人体组织中检测到TRID转录本,但在大多数检测的癌细胞系中未检测到。TRID的异位表达可保护哺乳动物细胞免受TRAIL诱导的凋亡,这与它的保护作用一致。还鉴定出另一种TRAIL的含死亡结构域受体(称为死亡受体-5),它优先激活一种与FLICE(半胱天冬酶-8)相关的死亡蛋白酶。

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