da Cunha A, Mintz M, Eiden L E, Sharer L R
Laboratory of Cell Biology, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, USA.
J Neuropathol Exp Neurol. 1997 Sep;56(9):974-87. doi: 10.1097/00005072-199709000-00003.
Progressive central nervous system dysfunction analogous to the AIDS dementia complex (ADC) seen in adults (HIV-1-associated progressive encephalopathy or HIV-1 encephalopathy) commonly occurs in HIV-1-infected children. The cause appears to be directly or indirectly related to HIV-1, rather than to other opportunistic pathogens. The exact mechanism(s) by which the virus affects brain function is not known. To determine whether the virus might modify brain function via an alteration in cortical neurons, we examined peptide neurotransmitter expression in the frontal cortex of HIV-1-infected cases with clinical HIV-1 encephalopathy relative to pathologic HIV-1 encephalitis. In situ hybridization was used to determine the level of peptide neurotransmitter expression of somatostatin in the frontal cortex of cases with and without HIV-1 encephalopathy and/or HIV-1 encephalitis. A 2-fold higher number of preprosomatostatin mRNA-positive interneurons was present in layer IV of cases with HIV-1 encephalitis compared with cases without HIV-1 encephalitis. In cases with PE, this neuronal alteration was 4- to 5-fold higher than in cases without PE, and was present in subcortical white matter in addition to layer IV. In cases having both PE and HIV-1 encephalitis, and in cases with HIV-1 encephalitis alone, these neuronal alterations in layer IV and/or subcortical white matter related to disseminated microglial nodules, even when these potentially viral-infected cells were negative for HIV-1 p24 antigen, a marker of productive viral infection. An alteration in preprosomatostatin mRNA-expressing cells occurring with HIV-1 encephalitis may be at least one mechanism that contributes to HIV-1 encephalopathy. When compared with other cortical laminae, layer IV receives most of its synaptic input from the mediodorsal nucleus of the thalamus. Neurons in the subcortical white matter project to the thalamus. The thalamus has been shown to have high amounts of viral antigen and increased metabolic activity in patients with AIDS. An alteration in preprosomatostatin mRNA-expressing cells may play a role in HIV-1 encephalopathy.
与成人中所见的艾滋病痴呆综合征(ADC)类似的进行性中枢神经系统功能障碍(HIV-1相关性进行性脑病或HIV-1脑病)在感染HIV-1的儿童中很常见。其病因似乎直接或间接与HIV-1有关,而非其他机会性病原体。病毒影响脑功能的确切机制尚不清楚。为了确定病毒是否可能通过改变皮质神经元来改变脑功能,我们研究了患有临床HIV-1脑病的HIV-1感染病例相对于病理性HIV-1脑炎的额叶皮质中肽类神经递质的表达。采用原位杂交法测定有无HIV-1脑病和/或HIV-1脑炎病例额叶皮质中生长抑素肽类神经递质的表达水平。与无HIV-1脑炎的病例相比,HIV-1脑炎病例的IV层中前促生长抑素原mRNA阳性中间神经元数量高出2倍。在患有进行性脑病(PE)的病例中,这种神经元改变比无PE的病例高4至5倍,并且除IV层外还存在于皮质下白质中。在同时患有PE和HIV-1脑炎的病例以及仅患有HIV-1脑炎的病例中,IV层和/或皮质下白质中的这些神经元改变与弥漫性小胶质结节有关,即使这些潜在的病毒感染细胞HIV-1 p24抗原呈阴性,而HIV-1 p24抗原是有活性病毒感染的标志物。HIV-1脑炎时前促生长抑素原mRNA表达细胞的改变可能至少是导致HIV-1脑病的一种机制。与其他皮质层相比,IV层大部分突触输入来自丘脑的内侧背核。皮质下白质中的神经元投射到丘脑。在艾滋病患者中,丘脑已被证明含有大量病毒抗原且代谢活性增加。前促生长抑素原mRNA表达细胞的改变可能在HIV-1脑病中起作用。