Akazawa Yohei, Vaidyanathan Sriram, Dewar Michael Bradley, Yazaki Kana, Dauz John, Honjo Osami, Sun Mei, Kabir Golam, Jankov Robert P, Heximer Scott Patrick, Connelly Kim A, Friedberg Mark K
Division of Cardiology, Labatt Family Heart Centre, Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Pediatrics, Stanford University, Stanford, California, USA.
JACC Basic Transl Sci. 2025 Mar;10(3):323-341. doi: 10.1016/j.jacbts.2024.10.007. Epub 2024 Dec 18.
Right ventricular (RV) pressure loading induces RV profibrotic signaling and fibrosis associated with RV dysfunction. RV decorin protein levels are decreased in patients with chronic RV pressure loading. RV decorin protein levels are also decreased in 4 animal models of mechanical RV pressure loading and pulmonary arterial hypertension. Human cardiac fibroblasts overexpressing decorin show diminished collagen-1 secretion in response to mechanical or chemical profibrotic stress while decorin knockout human cardiac fibroblasts show increased collagen-1 secretion in response to stress. Downregulation of decorin may play a key role in upregulating transforming growth factor-β1 profibrotic signaling and fibrosis that contribute to RV dysfunction in RV pressure loading.
右心室(RV)压力负荷可诱导RV促纤维化信号传导以及与RV功能障碍相关的纤维化。在慢性RV压力负荷患者中,RV核心蛋白聚糖的蛋白水平降低。在机械性RV压力负荷和肺动脉高压的4种动物模型中,RV核心蛋白聚糖的蛋白水平也降低。过表达核心蛋白聚糖的人心脏成纤维细胞在受到机械或化学促纤维化应激时,胶原蛋白-1分泌减少,而敲除核心蛋白聚糖的人心脏成纤维细胞在受到应激时,胶原蛋白-1分泌增加。核心蛋白聚糖的下调可能在上调转化生长因子-β1促纤维化信号传导和纤维化中起关键作用,而这会导致RV压力负荷时的RV功能障碍。