Chavanas Stéphane
Centre de Physiopathologie Toulouse Purpan, INSERM UMR 1043, Toulouse, France; CNRS UMR 5282 Toulouse, France; Université Paul Sabatier, Toulouse, France.
Neurogenesis (Austin). 2016 Sep 22;3(1):e1231654. doi: 10.1080/23262133.2016.1231654. eCollection 2016.
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.
人巨细胞病毒(HCMV)的先天性感染可能会导致永久性神经后遗症,包括感音神经性耳聋、脑瘫或严重的神经发育异常。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物激活受体γ(PPARγ)是发育中大脑HCMV发病机制的关键决定因素。利用来自人类胚胎干细胞的神经干细胞,我们发现HCMV感染会强烈增加神经干细胞中PPARγ的水平和活性。进一步的体外实验表明,PPARγ活性会抑制神经干细胞向神经元的神经源性分化。同样,在感染HCMV的胎儿脑切片中发现PPARγ表达增加,而在未感染的对照组中未发现。在这篇评论中,我们总结并讨论了我们的发现以及它们为HCMV先天性感染的神经发病机制提供的新见解。