Vieira Joaquim M, Riley Paul R
Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.
Br J Pharmacol. 2013 May;169(2):318-27. doi: 10.1111/j.1476-5381.2012.01928.x.
Over the last decade or so, intensive research in cardiac stem cell biology has led to significant discoveries towards a potential therapy for cardiovascular disease; the main cause of morbidity and mortality in humans. The major goal within the field of cardiovascular regenerative medicine is to replace lost or damaged cardiac muscle and coronaries following ischaemic disease. At present, de novo cardiomyocytes can be generated either in vitro, for cell transplantation or disease modelling using directed differentiation of embryonic stem cells or induced pluripotent stem cells, or in vivo via direct reprogramming of resident adult cardiac fibroblast or ectopic stimulation of resident cardiac stem or progenitor cells. A major bottleneck with all of these approaches is the low efficiency of cardiomyocyte differentiation alongside their relative functional immaturity. Chemical genetics, and the application of phenotypic screening with small molecule libraries, represent a means to enhance understanding of the molecular pathways controlling cardiovascular cell differentiation and, moreover, offer the potential for discovery of new drugs to invoke heart repair and regeneration. Here, we review the potential of chemical genetics in cardiac stem cell therapy, highlighting not only the major contributions to the field so far, but also the future challenges.
在过去十年左右的时间里,对心脏干细胞生物学的深入研究已取得重大发现,有望为心血管疾病(人类发病和死亡的主要原因)找到潜在疗法。心血管再生医学领域的主要目标是在缺血性疾病后替换受损或丢失的心肌和冠状动脉。目前,可以通过体外诱导胚胎干细胞或诱导多能干细胞定向分化来生成新的心肌细胞,用于细胞移植或疾病建模,也可以通过直接重编程成年心脏成纤维细胞或异位刺激心脏干细胞或祖细胞在体内生成新的心肌细胞。所有这些方法的一个主要瓶颈是心肌细胞分化效率低以及它们相对功能不成熟。化学遗传学以及小分子文库的表型筛选应用,是增强对控制心血管细胞分化分子途径理解的一种手段,此外,还为发现促进心脏修复和再生的新药提供了潜力。在此,我们回顾化学遗传学在心脏干细胞治疗中的潜力,不仅强调迄今为止该领域的主要贡献,还强调未来的挑战。