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作 者:Wattana Leowattana Tawithep Leowattana Pathomthep Leowattana
机构地区:[1]Department of Clinical Tropical Medicine,Faculty of Tropical Medicine,Mahidol University,Bangkok 10400,Thailand [2]Department of Medicine,Faculty of Medicine,Srinakharinwirot University,Bangkok 10110,Thailand
出 处:《World Journal of Clinical Cases》2022年第27期9588-9601,共14页世界临床病例杂志
摘 要:Patient-specific human-induced pluripotent stem cell-derived atrial cardiomyocytes(hiPSC-aCMs) may be produced,genome-edited,and differentiated into multiple cell types for regenerative medicine,disease modeling,drug testing,toxicity screening,and three-dimensional tissue fabrication.There is presently no complete model of atrial fibrillation(AF) available for studying human pharmacological responses and evaluating the toxicity of potential medication candidates.It has been demonstrated that hiPSC-aCMs can replicate the electrophysiological disease phenotype and genotype of AF.The hiPSC-aCMs,however,are immature and do not reflect the maturity of a CMs in the native myocardium.Numerous laboratories utilize a variety of methodologies and procedures to improve and promote a CM maturation,including electrical stimulation,culture duration,biophysical signals,and changes in metabolic variables.This review covers the current methods being explored for use in the maturation of patient-specific hiPSC-aCMs and their application towards a personalized approach to the pharmacologic therapy of AF.
关 键 词:Atrial fibrillation Human-induced pluripotent stem cell-derived atrial cardiomyocytes Disease modeling Maturation Pharmacologic response Personalized medicine
分 类 号:R541.75[医药卫生—心血管疾病]
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