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FAST-STEM: A Human pluripotent stem cell engineering toolkit for rapid design-build-test-learn development of human cell-based therapeutic devices

Aaron H. Rosenstein,Rangarajan Sambathkumar, Brandon M. Murareanu,Navroop K. Dhaliwal, Fumao Sun, Xinyaun Zhao, Abolfazl Dadvar,Rasha Al-attar, Andrew Chai,Nitya Gulati,Ting Yin,Maria Nguyen,Danielle Serra, Tania Devina, Aanshi Gandhi, Mohammad Saleh,Penney Gilbert,Tilo Kunath,Michael A. Laflamme,Shinichiro Ogawa,Julien Muffat,Yun Li,Stephanie Protze,Cristina Nostro,Michael Garton

crossref(2024)

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摘要
Very recent clinical advances in stem cell derived tissue replacement and gene therapy, in addition to the rise of artificial intelligence-aided scientific discovery, have placed the possibility of sophisticated human cell-based therapies firmly within reach. However, development of such cells and testing of their engineered gene circuit components, has proven highly challenging, due to the need for generating stable cell lines for each design–build–test–learn engineering cycle. Current approaches to generating stable human induced pluripotent stem cell (hiPSC) lines are highly time-consuming and suffer from lack of control, poor integration efficiency, and limited functionality. Validation in clinically relevant stem cell derived tissues is also broadly lacking. Such drawbacks are prohibitive to repeatably conducting cutting-edge stem cell engineering with broad application within a realistic timeframe and will not scale with the future of regenerative medicine. We have developed FAST-STEM ( F acile A ccelerated S tem-cell T ransgene integration with S ynBio T unable E ngineering M odes ), a hPSC engineering platform that drastically reduces the time to generate ‘differentiation ready’ stem cell lines from several weeks to 5 days, exhibiting a ~612-fold improvement in transgene integration rate over previous methodologies. Additional FAST-STEM innovations include: (i) rapid and highly efficient transgene integration; (ii) copy number control; (iii) simultaneous or consecutive integration of multiple gene cassettes; (iv) library screen capability. In addition to this unique functional versatility, platform transportability and broad use case for stem cell-engineering was confirmed by differentiation into eight different cell types across nine different laboratories. This platform dramatically lowers the bar for integration of synthetic biology with regenerative medicine, enabling experiments which were previously deemed logistically impossible, thus paving the way for sophisticated human cell device development. ### Competing Interest Statement The authors have declared no competing interest.
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