Mol E A, Goumans M J, Sluijter J P G
Department of Cardiology, Laboratory of Experimental Cardiology, University Medical Center Utrecht, Utrecht, 3584CX, The Netherlands.
Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, 2333ZA, The Netherlands.
Adv Exp Med Biol. 2017;998:207-219. doi: 10.1007/978-981-10-4397-0_14.
Cardiac progenitor cells (CPCs) have emerged as potential therapy to improve cardiac repair and prevent damage in cardiac diseases. CPCs are a promising cell source for cardiac therapy as they can generate all cardiovascular lineages in vitro and in vivo. Originating from the heart itself, CPCs may be destined to activate endogenous repair mechanisms. These CPCs release paracrine molecules that are able to stimulate cardiac repair mechanisms, including stimulation of vessel formation and inhibition of cardiomyocyte apoptosis. In addition to proteins and growth factors, CPCs release extracellular membrane vesicles, such as exosomes, which have gained increasing interest in recent years. Exosomal-derived miRNAs have been indicated to play an important role in these processes. Hereby, CPC exosomes can be considered as potential off-the-shelf therapeutics, as they are able to stimulate the regenerative capacity of the heart by increasing vessel density and lowering apoptosis of cardiomyocytes.
心脏祖细胞(CPCs)已成为改善心脏修复和预防心脏疾病损伤的潜在治疗方法。CPCs是心脏治疗中一种很有前景的细胞来源,因为它们能在体外和体内产生所有心血管谱系。CPCs起源于心脏本身,可能注定会激活内源性修复机制。这些CPCs释放旁分泌分子,能够刺激心脏修复机制,包括刺激血管形成和抑制心肌细胞凋亡。除了蛋白质和生长因子外,CPCs还释放细胞外膜泡,如外泌体,近年来人们对其兴趣与日俱增。已表明外泌体衍生的微小RNA(miRNAs)在这些过程中起重要作用。因此,CPC外泌体可被视为潜在的现成治疗剂,因为它们能够通过增加血管密度和降低心肌细胞凋亡来刺激心脏的再生能力。