| Literature DB >> 34992271 |
Daniël A Pijnappels1, Antoine A F de Vries2, Niels Harlaar1,3, Sven O Dekker1, Juan Zhang1, Rebecca R Snabel4, Marieke W Veldkamp5, Arie O Verkerk5,6, Carla Cofiño Fabres7, Verena Schwach7, Lente J S Lerink1, Mathilde R Rivaud5, Aat A Mulder8, Willem E Corver9, Marie José T H Goumans8, Dobromir Dobrev10, Robert J M Klautz3, Martin J Schalij1, Gert Jan C Veenstra4, Robert Passier7, Thomas J van Brakel3.
Abstract
The lack of a scalable and robust source of well-differentiated human atrial myocytes constrains the development of in vitro models of atrial fibrillation (AF). Here we show that fully functional atrial myocytes can be generated and expanded one-quadrillion-fold via a conditional cell-immortalization method relying on lentiviral vectors and the doxycycline-controlled expression of a recombinant viral oncogene in human foetal atrial myocytes, and that the immortalized cells can be used to generate in vitro models of AF. The method generated 15 monoclonal cell lines with molecular, cellular and electrophysiological properties resembling those of primary atrial myocytes. Multicellular in vitro models of AF generated using the immortalized atrial myocytes displayed fibrillatory activity (with activation frequencies of 6-8 Hz, consistent with the clinical manifestation of AF), which could be terminated by the administration of clinically approved antiarrhythmic drugs. The conditional cell-immortalization method could be used to generate functional cell lines from other human parenchymal cells, for the development of in vitro models of human disease.Entities:
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Year: 2022 PMID: 34992271 DOI: 10.1038/s41551-021-00827-5
Source DB: PubMed Journal: Nat Biomed Eng ISSN: 2157-846X Impact factor: 29.234