Department of Developmental Genetics, Max Planck Institute for Heart and Lung Research, Bad Nauheim 61231, Germany.
Institute of Cell Biology, Faculty of Medicine, University of Münster, Münster 48149, Germany.
Development. 2024 Jul 1;151(13). doi: 10.1242/dev.202310. Epub 2024 Jul 10.
The cardiac extracellular matrix (cECM) is fundamental for organ morphogenesis and maturation, during which time it undergoes remodeling, yet little is known about whether mechanical forces generated by the heartbeat regulate this remodeling process. Using zebrafish as a model and focusing on stages when cardiac valves and trabeculae form, we found that altering cardiac contraction impairs cECM remodeling. Longitudinal volumetric quantifications in wild-type animals revealed region-specific dynamics: cECM volume decreases in the atrium but not in the ventricle or atrioventricular canal. Reducing cardiac contraction resulted in opposite effects on the ventricular and atrial ECM, whereas increasing the heart rate affected the ventricular ECM but had no effect on the atrial ECM, together indicating that mechanical forces regulate the cECM in a chamber-specific manner. Among the ECM remodelers highly expressed during cardiac morphogenesis, we found one that was upregulated in non-contractile hearts, namely tissue inhibitor of matrix metalloproteinase 2 (timp2). Loss- and gain-of-function analyses of timp2 revealed its crucial role in cECM remodeling. Altogether, our results indicate that mechanical forces control cECM remodeling in part through timp2 downregulation.
心脏细胞外基质(cECM)对于器官形态发生和成熟至关重要,在此期间它经历重塑,但对于心跳产生的机械力是否调节这种重塑过程知之甚少。本研究以斑马鱼为模型,重点研究心脏瓣膜和小梁形成的阶段,发现改变心脏收缩会损害 cECM 的重塑。在野生型动物的纵向体积定量分析中揭示了区域特异性动力学:心房中的 cECM 体积减少,但心室或房室管中没有减少。减少心脏收缩对心室和心房 ECM 产生相反的影响,而增加心率则影响心室 ECM,但对心房 ECM 没有影响,这表明机械力以腔室特异性的方式调节 cECM。在心脏形态发生过程中高度表达的 ECM 重塑剂中,我们发现有一种在非收缩性心脏中上调的物质,即基质金属蛋白酶组织抑制剂 2(timp2)。timp2 的缺失和功能获得分析揭示了其在 cECM 重塑中的关键作用。总之,我们的结果表明,机械力通过下调 timp2 来控制 cECM 的重塑。