Institute of Biochemistry and Molecular Biology II, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Stem Cell Biology, and Regenerative Medicine Research Group, Institute of Biotechnology, Ferdowsi University of Mashhad, Mashhad 91779-48974, Iran.
Cells. 2023 Jul 4;12(13):1780. doi: 10.3390/cells12131780.
Pathological cardiac hypertrophy is a key risk factor for the development of heart failure and predisposes individuals to cardiac arrhythmia and sudden death. While physiological cardiac hypertrophy is adaptive, hypertrophy resulting from conditions comprising hypertension, aortic stenosis, or genetic mutations, such as hypertrophic cardiomyopathy, is maladaptive. Here, we highlight the essential role and reciprocal interactions involving both cardiomyocytes and non-myocardial cells in response to pathological conditions. Prolonged cardiovascular stress causes cardiomyocytes and non-myocardial cells to enter an activated state releasing numerous pro-hypertrophic, pro-fibrotic, and pro-inflammatory mediators such as vasoactive hormones, growth factors, and cytokines, i.e., commencing signaling events that collectively cause cardiac hypertrophy. Fibrotic remodeling is mediated by cardiac fibroblasts as the central players, but also endothelial cells and resident and infiltrating immune cells enhance these processes. Many of these hypertrophic mediators are now being integrated into computational models that provide system-level insights and will help to translate our knowledge into new pharmacological targets. This perspective article summarizes the last decades' advances in cardiac hypertrophy research and discusses the herein-involved complex myocardial microenvironment and signaling components.
病理性心肌肥厚是心力衰竭发展的一个关键风险因素,使个体易患心律失常和猝死。虽然生理性心肌肥厚是适应性的,但由高血压、主动脉瓣狭窄或肥厚型心肌病等遗传突变引起的肥厚则是失调性的。在这里,我们强调了在病理性条件下,心肌细胞和非心肌细胞所涉及的重要作用和相互作用。长期的心血管应激导致心肌细胞和非心肌细胞进入激活状态,释放大量促肥厚、促纤维化和促炎介质,如血管活性激素、生长因子和细胞因子,即启动共同导致心肌肥厚的信号事件。纤维化重塑由心脏成纤维细胞作为核心参与者介导,但内皮细胞和驻留和浸润的免疫细胞也增强了这些过程。许多这些肥厚介质现在被整合到计算模型中,提供系统水平的见解,并将有助于将我们的知识转化为新的药理学靶点。本文总结了过去几十年心肌肥厚研究的进展,并讨论了其中涉及的复杂心肌微环境和信号成分。