Department of Cell Biology, Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710, USA.
Dev Biol. 2012 May 15;365(2):319-27. doi: 10.1016/j.ydbio.2012.02.018. Epub 2012 Feb 20.
Zebrafish regenerate cardiac muscle after severe injuries through the activation and proliferation of spared cardiomyocytes. Little is known about factors that control these events. Here we investigated the extent to which miRNAs regulate zebrafish heart regeneration. Microarray analysis identified many miRNAs with increased or reduced levels during regeneration. miR-133, a miRNA with known roles in cardiac development and disease, showed diminished expression during regeneration. Induced transgenic elevation of miR-133 levels after injury inhibited myocardial regeneration, while transgenic miR-133 depletion enhanced cardiomyocyte proliferation. Expression analyses indicated that cell cycle factors mps1, cdc37, and PA2G4, and cell junction components cx43 and cldn5, are miR-133 targets during regeneration. Using pharmacological inhibition and EGFP sensor interaction studies, we found that cx43 is a new miR-133 target and regeneration gene. Our results reveal dynamic regulation of miRNAs during heart regeneration, and indicate that miR-133 restricts injury-induced cardiomyocyte proliferation.
斑马鱼通过激活和增殖剩余的心肌细胞来再生严重损伤的心肌。目前尚不清楚控制这些事件的因素。在这里,我们研究了 microRNAs 在多大程度上调控斑马鱼心脏再生。微阵列分析鉴定出许多在再生过程中表达水平增加或降低的 microRNAs。miR-133 是一种在心脏发育和疾病中具有已知作用的 microRNA,在再生过程中表达水平降低。损伤后诱导转基因 miR-133 水平升高抑制心肌再生,而转基因 miR-133 耗竭增强心肌细胞增殖。表达分析表明,细胞周期因子 mps1、cdc37 和 PA2G4 以及细胞连接成分 cx43 和 cldn5 是再生过程中的 miR-133 靶标。通过药理学抑制和 EGFP 传感器相互作用研究,我们发现 cx43 是 miR-133 的一个新的靶标和再生基因。我们的结果揭示了 microRNAs 在心脏再生过程中的动态调控,并表明 miR-133 限制了损伤诱导的心肌细胞增殖。