Department of Pharmacology and Experimental Neuroscience, Radiology, Surgery, and Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska 68198, USA.
J Neurosci. 2011 Mar 2;31(9):3148-57. doi: 10.1523/JNEUROSCI.5473-10.2011.
Neuronal damage induced by ongoing human immunodeficiency virus type 1 (HIV-1) infection was investigated in humanized NOD/scid-IL-2Rγ(c)(null) mice transplanted at birth with human CD34-positive hematopoietic stem cells. Mice infected at 5 months of age and followed for up to 15 weeks maintained significant plasma viral loads and showed reduced numbers of CD4(+) T-cells. Prospective serial proton magnetic resonance spectroscopy tests showed selective reductions in cortical N-acetyl aspartate in infected animals. Diffusion tensor imaging revealed structural changes in cortical gray matter. Postmortem immunofluorescence brain tissue examinations for neuronal and glial markers, captured by multispectral imaging microscopy and quantified by morphometric and fluorescence emission, showed regional reduction of neuronal soma and synaptic architectures. This was evidenced by loss of microtubule-associated protein 2, synaptophysin, and neurofilament antigens. This study is the first, to our knowledge, demonstrating lost neuronal integrity after HIV-1 infection in humanized mice. As such, the model permits studies of the relationships between ongoing viral replication and virus-associated neurodegeneration.
本研究旨在探讨持续的人类免疫缺陷病毒 1 型(HIV-1)感染对人类化 NOD/scid-IL-2Rγ(c)(null)小鼠(在出生时移植了人源 CD34 阳性造血干细胞)造成的神经元损伤。将 5 月龄的小鼠进行感染,并对其进行长达 15 周的随访,结果显示这些小鼠持续保持较高的血浆病毒载量,并出现 CD4+T 细胞数量减少的情况。前瞻性连续质子磁共振波谱检测显示,感染动物的皮质 N-乙酰天门冬氨酸选择性减少。弥散张量成像显示皮质灰质存在结构变化。通过多光谱成像显微镜捕获和形态计量学及荧光发射定量的神经元和神经胶质标志物的免疫荧光脑组织检查显示,神经元胞体和突触结构的区域减少。这一结果可通过微管相关蛋白 2、突触素和神经丝抗原的丢失来证明。本研究首次证明了人类化小鼠在 HIV-1 感染后存在神经元完整性丧失。因此,该模型允许研究持续病毒复制与病毒相关神经退行性变之间的关系。