Summary Ectopic expression of proteins in human pluripotent stem cells (hPSCs) is highly desirable as a research tool and important for clinical translation. However, genetically engineering hPSCs for long-term overexpression of proteins remains inefficient, labor-intensive, and plagued by epigenetic silencing, necessitating dedication of significant resources, and entailing laborious workflows. To address these limitations, we report the development of XPRESSO (expedited persistent and robust engineering of stem cells with sleeping beauty for overexpression), a modular “anti-silencing” transposon vector, which we have combined with a highly efficient and accessible methodology for the rapid generation of genetically modified hPSC lines in a gene-independent manner. Using this method, we successfully generated dozens of stable hPSC lines with robust and continuous functional expression of optogenetic proteins, Cas9, shRNA, and a calcium indicator in both undifferentiated and differentiated (cardiomyocyte and neuronal) cells.
XPRESSO: Rapid genetic engineering of human pluripotent stem cells for durable overexpression using a modular anti-silencing vector
Yehuda Wexler,Harel Grinstein,I. Huber,S. Glatstein,Matteo Ghiringhelli,Oded Edri,M. Landesberg,Daniel Shiff,G. Arbel,Idan Rosh,Ashwani Choudhary,S. Stern,L. Gepstein
Published 2025 in Stem Cell Reports
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- Publication year
2025
- Venue
Stem Cell Reports
- Publication date
2025-08-01
- Fields of study
Medicine, Engineering
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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