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

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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436085/
https://www.ncbi.nlm.nih.gov/pubmed/30949028
http://dx.doi.org/10.3389/fncel.2019.00064
Descripción
Sumario: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.