Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/361660
Type: Artigo
Title: Rhesus IPSC safe harbor gene-editing platform for stable expression of transgenes in differentiated cells of all germ layers
Author: Hong, So Gun
Yada, Ravi Chandra
Choi, Kyujoo
Carpentier, Arnaud
Liang, T. Jake
Merling, Randall K.
Sweeney, Colin L.
Malech, Harry L.
Jung, Moonjung
Corat, Marcus A. F.
AlJanahi, Aisha A.
Lin, Yongshun
Liu, Huimin
Tunc, Ilker
Wang, Xujing
Palisoc, Maryknoll
Pittaluga, Stefania
Boehm, Manfred
Winkler, Thomas
Zou, Jizhong
Dunbar, Cynthia E.
Abstract: Nonhuman primate (NHP) induced pluripotent stem cells (iPSCs) offer the opportunity to investigate the safety, feasibility, and efficacy of proposed iPSC-derived cellular delivery in clinically relevant in vivo models. However, there is need for stable, robust, and safe labeling methods for NHP iPSCs and their differentiated lineages to study survival, proliferation, tissue integration, and biodistribution following transplantation. Here we investigate the utility of the adenoassociated virus integration site 1 (AAVS1) as a safe harbor for the addition of transgenes in our rhesus macaque iPSC (RhiPSC) model. A clinically relevant marker gene, human truncated CD19 (h Delta CD19), or GFP was inserted into the AAVS1 site in RhiPSCs using the CRISPR/Cas9 system. Genetically modified RhiPSCs maintained normal karyotype and pluripotency, and these clones were able to further differentiate into all three germ layers in vitro and in vivo. In contrast to transgene delivery using randomly integrating viral vectors, AAVS1 targeting allowed stable transgene expression following differentiation. Off -target mutations were observed in some edited clones, highlighting the importance of careful characterization of these cells prior to downstream applications. Genetically marked RhiPSCs will be useful to further advance clinically relevant models for iPSC-based cell therapies
Subject: Células-tronco embrionárias
Country: Estados Unidos
Editor: Cell Press
Citation: Division of Intramural Research at the National Heart, Lung and Blood Institute (NHLBI) at the NIH; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Heart Lung & Blood Institute (NHLBI); NIH National Institute of Allergy & Infectious Diseases (NIAID); NIH National Institute of Diabetes & Digestive & Kidney Diseases (NIDDK)
Rights: Fechado
Identifier DOI: 10.1016/j.ymthe.2016.10.007
Address: https://www.sciencedirect.com/science/article/pii/S152500161645361X
Date Issue: 2017
Appears in Collections:CEMIB - Artigos e Outros Documentos

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