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寨卡病毒损害人类神经干细胞和神经元中的神经发生及突触发生途径。

Zika Virus Impairs Neurogenesis and Synaptogenesis Pathways in Human Neural Stem Cells and Neurons.

作者信息

Rosa-Fernandes Livia, Cugola Fernanda Rodrigues, Russo Fabiele Baldino, Kawahara Rebeca, de Melo Freire Caio Cesar, Leite Paulo Emílio Corrêa, Bassi Stern Ana Carolina, Angeli Claudia Blanes, de Oliveira Danielle Bruna Leal, Melo Stella Rezende, Zanotto Paolo Marinho de Andrade, Durigon Edison Luiz, Larsen Martin Røssel, Beltrão-Braga Patricia Cristina Baleeiro, Palmisano Giuseppe

机构信息

Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.

Department of Microbiology, Institute of Biomedical Science, University of São Paulo, São Paulo, Brazil.

出版信息

Front Cell Neurosci. 2019 Mar 15;13:64. doi: 10.3389/fncel.2019.00064. eCollection 2019.

Abstract

Growing evidences have associated Zika virus (ZIKV) infection with congenital malformations, including microcephaly. Nonetheless, signaling mechanisms that promote the disease outcome are far from being understood, affecting the development of suitable therapeutics. In this study, we applied shotgun mass spectrometry (MS)-based proteomics combined with cell biology approaches to characterize altered molecular pathways on human neuroprogenitor cells (NPC) and neurons derived from induced pluripotent stem cells infected by ZIKV-BR strain, obtained from the 2015 Brazilian outbreak. Furthermore, ZIKV-BR infected NPCs showed unique alteration of pathways involved in neurological diseases, cell death, survival and embryonic development compared to ZIKV-AF, showing a human adaptation of the Brazilian viral strain. Besides, infected neurons differentiated from NPC presented an impairment of neurogenesis and synaptogenesis processes. Taken together, these data explain that CNS developmental arrest observed in Congenital Zika Syndrome is beyond neuronal cell death.

摘要

越来越多的证据表明,寨卡病毒(ZIKV)感染与包括小头畸形在内的先天性畸形有关。然而,促进疾病发生的信号传导机制仍远未被了解,这影响了合适治疗方法的开发。在本研究中,我们应用基于鸟枪法质谱(MS)的蛋白质组学并结合细胞生物学方法,来表征来自诱导多能干细胞的人类神经祖细胞(NPC)和神经元中分子途径的改变,这些细胞被从2015年巴西疫情中分离出的ZIKV-BR毒株感染。此外,与ZIKV-AF相比,ZIKV-BR感染的NPC在神经疾病、细胞死亡、存活和胚胎发育相关途径中表现出独特的改变,表明巴西病毒株存在人类适应性。此外,从NPC分化而来的受感染神经元在神经发生和突触形成过程中出现损伤。综上所述,这些数据表明,先天性寨卡综合征中观察到的中枢神经系统发育停滞不仅仅是神经元细胞死亡所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bd3/6436085/e51d55740830/fncel-13-00064-g001.jpg

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