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Arrhythmia Mechanisms in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes

期刊

JOURNAL OF CARDIOVASCULAR PHARMACOLOGY
卷 77, 期 3, 页码 300-316

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/FJC.0000000000000972

关键词

hiPSC-CM; arrhythmia mechanisms; in vitro; in silico

资金

  1. Academy of Finland (project CardSiPop) [307967]
  2. Finnish Cultural Foundation (Central Fund) [00160735, 00180843]
  3. Aarne Koskelo Foundation
  4. Finnish Foundation for Cardiovascular Research [170070]
  5. Pirkanmaa Regional Fund of the Finnish Cultural Foundation [50171514, 50201322]
  6. Academy of Finland (AKA) [307967, 307967] Funding Source: Academy of Finland (AKA)

向作者/读者索取更多资源

The advent of human induced pluripotent stem cell-derived cardiomyocytes has provided a new avenue for studying cardiac arrhythmias, with potential applications in personalized medicine and regenerative medicine. This novel modeling system offers insights into arrhythmogenic triggers and substrates, while also opening doors for future possibilities in the field.
Despite major efforts by clinicians and researchers, cardiac arrhythmia remains a leading cause of morbidity and mortality in the world. Experimental work has relied on combining high-throughput strategies with standard molecular and electrophysiological studies, which are, to a great extent, based on the use of animal models. Because this poses major challenges for translation, the progress in the development of novel antiarrhythmic agents and clinical care has been mostly disappointing. Recently, the advent of human induced pluripotent stem cell-derived cardiomyocytes has opened new avenues for both basic cardiac research and drug discovery; now, there is an unlimited source of cardiomyocytes of human origin, both from healthy individuals and patients with cardiac diseases. Understanding arrhythmic mechanisms is one of the main use cases of human induced pluripotent stem cell-derived cardiomyocytes, in addition to pharmacological cardiotoxicity and efficacy testing, in vitro disease modeling, developing patient-specific models and personalized drugs, and regenerative medicine. Here, we review the advances that the human induced pluripotent stem cell-derived-based modeling systems have brought so far regarding the understanding of both arrhythmogenic triggers and substrates, while also briefly speculating about the possibilities in the future.

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