Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX, USA.
Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX, USA.
J Mol Cell Cardiol. 2023 May;178:51-58. doi: 10.1016/j.yjmcc.2023.03.008. Epub 2023 Mar 23.
Cardiovascular disease is one of the leading causes of morbidity and mortality worldwide, with myocardial infarctions being amongst the deadliest manifestations. Reduced blood flow to the heart can result in the death of cardiac tissue, leaving affected patients susceptible to further complications and recurrent disease. Further, contemporary management typically involves a pharmacopeia to manage the metabolic conditions contributing to atherosclerotic and hypertensive heart disease, rather than regeneration of the damaged myocardium. With modern healthcare extending lifespan, a larger demographic will be at risk for heart disease, driving the need for novel therapeutics that surpass those currently available in efficacy. Transdifferentiation and cellular reprogramming have been looked to as potential methods for the treatment of diseases throughout the body. Specifically targeting the fibrotic cells in cardiac scar tissue as a source to be reprogrammed into induced cardiomyocytes remains an appealing option. This review aims to highlight the history of and advances in cardiac reprogramming and describe its translational potential as a treatment for cardiovascular disease.
心血管疾病是全球发病率和死亡率的主要原因之一,心肌梗死是其中最致命的表现之一。心脏血流减少会导致心肌组织死亡,使受影响的患者容易发生进一步的并发症和疾病复发。此外,目前的治疗方法通常涉及使用药物来治疗导致动脉粥样硬化和高血压性心脏病的代谢状况,而不是再生受损的心肌。随着现代医疗保健延长寿命,更大的人群将面临心脏病的风险,这就需要新的治疗方法,其疗效要超过目前可用的治疗方法。转分化和细胞重编程已被视为治疗全身疾病的潜在方法。具体来说,将心脏疤痕组织中的成纤维细胞作为一种可被重新编程为诱导心肌细胞的来源,仍然是一种有吸引力的选择。本综述旨在强调心脏重编程的历史和进展,并描述其作为心血管疾病治疗方法的转化潜力。