| Literature DB >> 30686581 |
Yimu Zhao1, Naimeh Rafatian2, Nicole T Feric3, Brian J Cox4, Roozbeh Aschar-Sobbi5, Erika Yan Wang6, Praful Aggarwal7, Boyang Zhang8, Genevieve Conant8, Kacey Ronaldson-Bouchard9, Aric Pahnke8, Stephanie Protze10, Jee Hoon Lee11, Locke Davenport Huyer8, Danica Jekic12, Anastasia Wickeler13, Hani E Naguib13, Gordon M Keller14, Gordana Vunjak-Novakovic15, Ulrich Broeckel7, Peter H Backx16, Milica Radisic17.
Abstract
Tissue engineering using cardiomyocytes derived from human pluripotent stem cells holds a promise to revolutionize drug discovery, but only if limitations related to cardiac chamber specification and platform versatility can be overcome. We describe here a scalable tissue-cultivation platform that is cell source agnostic and enables drug testing under electrical pacing. The plastic platform enabled on-line noninvasive recording of passive tension, active force, contractile dynamics, and Ca2+ transients, as well as endpoint assessments of action potentials and conduction velocity. By combining directed cell differentiation with electrical field conditioning, we engineered electrophysiologically distinct atrial and ventricular tissues with chamber-specific drug responses and gene expression. We report, for the first time, engineering of heteropolar cardiac tissues containing distinct atrial and ventricular ends, and we demonstrate their spatially confined responses to serotonin and ranolazine. Uniquely, electrical conditioning for up to 8 months enabled modeling of polygenic left ventricular hypertrophy starting from patient cells.Entities:
Keywords: Cardiomyocyte; action potential; atrial; calcium transient; contractility; drug testing; electrophysiology; heart; polygenic cardiac disease; tissue engineering; ventricular
Mesh:
Year: 2019 PMID: 30686581 PMCID: PMC6456036 DOI: 10.1016/j.cell.2018.11.042
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582