Reduction in phosphorylated heavy neurofilament in the cerebellum in HIV disease.

I P Everall, H Barnes
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引用次数: 2

Abstract

In the absence of significant neuronal infection HIV induces neuronal damage and death. The pathogenesis of this process is not clear and can only be assessed in the HIV infected brain by examining surviving neuronal populations. Cerebellar Purkinje cells are a model population. We have already demonstrated glutamate receptor alterations in these neurons in AIDS, and in the current study we have investigated the phosphorylation status of heavy neurofilament (NF-H), which is under the control of various intracellular kinases. While the number of Purkinje cells expressing non-phosphorylated NF-H was unchanged, the number of Purkinje cells expressing phosphorylated NF-H was decreased by 36% in the HIV group. This may be a marker of neuronal damage, and possibly indicate alteration in the activity of various intracellular signalling kinase pathways in the HIV infected brain.

HIV疾病中小脑磷酸化重神经丝的减少。
在没有显著的神经元感染的情况下,HIV诱导神经元损伤和死亡。这一过程的发病机制尚不清楚,只能通过检查存活的神经元群在HIV感染的大脑中进行评估。小脑浦肯野细胞是一种模型细胞群。我们已经证明了艾滋病患者这些神经元中谷氨酸受体的改变,在目前的研究中,我们研究了重神经丝(NF-H)的磷酸化状态,这是在各种细胞内激酶的控制下。虽然表达非磷酸化NF-H的浦肯野细胞数量不变,但在HIV组中表达磷酸化NF-H的浦肯野细胞数量减少了36%。这可能是神经元损伤的标志,并可能表明在HIV感染的大脑中,各种细胞内信号激酶途径的活性发生了变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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