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Efficient Recombinase-mediated Cassette Exchange in Hpscs to Study the Hepatocyte Lineage Reveals AAVS1 Locus-mediated Transgene Inhibition
Laura Ordovás
Ruben Boon
Mariaelena Pistoni
Yemiao Chen
Esther Wolfs
Wenting Guo
Rangarajan Sambathkumar
Sylwia Bobis-Wozowicz
Nicky Helsen
Jolien Vanhove
Pieter Berckmans
Qing Cai
Kim Vanuytsel
Kristel Eggermont
Veerle Vanslembrouck
Béla Z. Schmidt
Susanna Raitano
Ludo van den Bosch
Yaakov Nahmias
Anton Cathomen
Tom Struys
Catherine M Verfaillie
出版
Universität
, 2015
URL
http://books.google.com.hk/books?id=96d4zgEACAAJ&hl=&source=gbs_api
註釋
Abstract: Tools for rapid and efficient transgenesis in "safe harbor" loci in an isogenic context remain important to exploit the possibilities of human pluripotent stem cells (hPSCs). We created hPSC master cell lines suitable for FLPe recombinase-mediated cassette exchange (RMCE) in the AAVS1 locus that allow generation of transgenic lines within 15 days with 100% efficiency and without random integrations. Using RMCE, we successfully incorporated several transgenes useful for lineage identification, cell toxicity studies, and gene overexpression to study the hepatocyte lineage. However, we observed unexpected and variable transgene expression inhibition in vitro, due to DNA methylation and other unknown mechanisms, both in undifferentiated hESC and differentiating hepatocytes. Therefore, the AAVS1 locus cannot be considered a universally safe harbor locus for reliable transgene expression in vitro, and using it for transgenesis in hPSC will require careful assessment of the function of individual transgenes