Ranki A, Nyberg M, Ovod V, Haltia M, Elovaara I, Raininko R, Haapasalo H, Krohn K
Department of Dermatology and Venereal Diseases, University of Helsinki, Finland.
AIDS. 1995 Sep;9(9):1001-8. doi: 10.1097/00002030-199509000-00004.
To relate the expression of HIV regulatory proteins and HIV-specific mRNA in the brain cells of infected individuals with clinical neurological disease.
Formalin-fixed postmortem brain tissue from 14 HIV-infected adult patients, with previous repeated neurological and neuroradiological examinations, was studied by immunohistochemical and molecular biological methods. Samples from non-infected brains served as controls.
Immunohistochemistry with monoclonal antibodies (MAb) was combined with in situ RNA hybridization. Target cells were identified with MAb to glial fibrillary acidic protein (GFAP; astrocytes), CD68 (activated macrophages) and Ricinus communis agglutinin (RCA-1; microglia, endothelial cells). For HIV, a panel of MAb against HIV Nef, Tat, Rev and Env proteins or probes specific for all classes of mRNA (nef), for singly or non-spliced mRNA (env) and for non-spliced mRNA (gag/pol) were used.
Nef protein was detected in subcortical or subpial astrocytes in seven out of 14 samples, and in multinucleated giant cells in two cases. Gag/pol or env mRNA-expressing astrocytes were detected in four cases. In four out of five cases studied, HIV Rev, but not Tat, was also expressed in astrocytes. Six out of the seven patients with Nef-positive astrocytes had suffered from moderate to severe dementia. The patient with most rapidly progressing severe dementia showed extensive HIV mRNA expression together with Nef and Rev expression in astrocytes.
In adult human brain, astrocytes are infected by HIV and preferentially express HIV Nef and Rev proteins but are also sometimes productively infected. Astrocyte infection is associated with moderate to severe dementia which agrees with recent knowledge on the housekeeping activities of astrocytes and their eventual role in learning and memory.
将感染个体脑细胞中HIV调节蛋白和HIV特异性mRNA的表达与临床神经疾病联系起来。
采用免疫组织化学和分子生物学方法,对14例有多次神经学和神经放射学检查史的HIV感染成年患者的福尔马林固定尸检脑组织进行研究。未感染大脑的样本作为对照。
将单克隆抗体(MAb)免疫组织化学与原位RNA杂交相结合。用针对胶质纤维酸性蛋白(GFAP;星形胶质细胞)、CD68(活化巨噬细胞)和蓖麻凝集素(RCA-1;小胶质细胞、内皮细胞)的MAb鉴定靶细胞。对于HIV,使用一组针对HIV Nef、Tat、Rev和Env蛋白的MAb或针对所有mRNA类别(nef)、单剪接或未剪接mRNA(env)以及未剪接mRNA(gag/pol)的探针。
14个样本中有7个在皮质下或软膜下星形胶质细胞中检测到Nef蛋白,2例在多核巨细胞中检测到。4例检测到表达gag/pol或env mRNA的星形胶质细胞。在研究的5例中有4例,HIV Rev而非Tat也在星形胶质细胞中表达。7例Nef阳性星形胶质细胞患者中有6例患有中度至重度痴呆。患有进展最迅速的重度痴呆的患者在星形胶质细胞中显示出广泛的HIV mRNA表达以及Nef和Rev表达。
在成人大脑中,星形胶质细胞被HIV感染,优先表达HIV Nef和Rev蛋白,但有时也会被有效感染。星形胶质细胞感染与中度至重度痴呆有关,这与最近关于星形胶质细胞的管家活动及其在学习和记忆中的最终作用的知识一致。