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肿瘤坏死因子相关凋亡诱导配体介导人类神经元凋亡:与HIV-1相关痴呆的联系。

TNF-related apoptosis-inducing ligand mediates human neuronal apoptosis: links to HIV-1-associated dementia.

作者信息

Ryan Lisa A, Peng Hui, Erichsen David A, Huang Yunlong, Persidsky Yuri, Zhou You, Gendelman Howard E, Zheng Jialin

机构信息

Laboratory of Neurotoxicology, University of Nebraska Medical Center, Omaha, NE 68195-5215, USA.

出版信息

J Neuroimmunol. 2004 Mar;148(1-2):127-39. doi: 10.1016/j.jneuroim.2003.11.019.

Abstract

TNF-related apoptosis-inducing ligand (TRAIL) is a type II integral membrane protein that interacts with multiple receptors and cell types including neurons. In this report, TRAIL protein levels were increased in human monocyte-derived macrophages (MDM) after HIV-1 infection and immune activation. In HIV-1 encephalitic (HIVE) human brain tissue, TRAIL-expressing macrophages were found in association with active caspase-3 positive neurons. Cytotoxic TRAIL receptors 1 and 2 were expressed on neurons in primary human fetal cultures and HIV-1 encephalitic brain tissue. Furthermore, TRAIL induced a dose-dependent effect on neuronal apoptosis. These results support a role for TRAIL in mononuclear phagocyte (MP)-mediated neurotoxicity in HIV-1-associated dementia (HAD).

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL)是一种II型整合膜蛋白,可与包括神经元在内的多种受体和细胞类型相互作用。在本报告中,HIV-1感染和免疫激活后人单核细胞衍生巨噬细胞(MDM)中TRAIL蛋白水平升高。在HIV-1脑炎性(HIVE)人脑组织中,发现表达TRAIL的巨噬细胞与活性半胱天冬酶-3阳性神经元相关。细胞毒性TRAIL受体1和2在原代人胎儿培养物和HIV-1脑炎性脑组织的神经元上表达。此外,TRAIL对神经元凋亡具有剂量依赖性作用。这些结果支持TRAIL在HIV-1相关痴呆(HAD)中单核吞噬细胞(MP)介导的神经毒性中的作用。

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