Ryan Lisa A, Peng Hui, Erichsen David A, Huang Yunlong, Persidsky Yuri, Zhou You, Gendelman Howard E, Zheng Jialin
Laboratory of Neurotoxicology, University of Nebraska Medical Center, Omaha, NE 68195-5215, USA.
J Neuroimmunol. 2004 Mar;148(1-2):127-39. doi: 10.1016/j.jneuroim.2003.11.019.
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).
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。