过氧化物酶体增殖物激活受体γ (PPARγ)激活:先天性巨细胞病毒感染期间神经发病的关键决定因素

S. Chavanas
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引用次数: 3

摘要

先天性巨细胞病毒(HCMV)感染可导致永久性神经系统后遗症,包括感音神经性耳聋、脑瘫或破坏性神经发育异常。我们最近发现,核受体超家族的转录因子过氧化物酶体增殖体激活受体γ (PPARγ)是发育中的大脑HCMV发病机制的关键决定因素。利用人胚胎干细胞提取的神经干细胞,我们发现HCMV感染可显著增加NSCs中PPARγ的水平和活性。进一步的体外实验表明,PPARγ活性抑制NSCs向神经元的神经源性分化。一致地,在感染HCMV的胎儿脑切片中发现PPARγ表达增加,但在未感染的对照组中没有。在这篇评论中,我们总结和讨论了我们的发现以及他们提供的关于HCMV先天性感染的神经发病机制的新见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peroxisome proliferator-activated receptor γ (PPARγ) activation: A key determinant of neuropathogeny during congenital infection by cytomegalovirus
ABSTRACT Congenital infection by human cytomegalovirus (HCMV) might result in permanent neurological sequelae, including sensorineural deafness, cerebral palsies or devastating neurodevelopmental abnormalities. We recently disclosed that Peroxisome Proliferator-Activated Receptor gamma (PPARγ), a transcription factor of the nuclear receptor superfamily, is a key determinant of HCMV pathogenesis in developing brain. Using neural stem cells from human embryonic stem cells, we showed that HCMV infection strongly increases levels and activity of PPARγ in NSCs. Further in vitro experiments showed that PPARγ activity inhibits the neuronogenic differentiation of NSCs into neurons. Consistently, increased PPARγ expression was found in brain section of fetuses infected by HCMV, but not in uninfected controls. In this commentary, we summarize and discuss our findings and the new insights they provide on the neuropathogenesis of HCMV congenital infection.
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