Department of Pathophysiology, China-Japan Collaborative Lab of Cardiovascular Physiology and Key Lab of Shock and Microcirculation Research, Southern Medical University, 1838 Guangzhou Avenue North, Guangzhou 510515, China.
Biochem Biophys Res Commun. 2010 Mar 12;393(3):519-25. doi: 10.1016/j.bbrc.2010.02.039. Epub 2010 Feb 10.
This study was aimed to investigate whether the antihypertrophic effects of adiponectin in murine hearts are associated with the modulation of HB-EGF signaling. We determined the myocardial expressions of adiponectin and adiponectin receptors, brain natriuretic peptide (BNP), and HB-EGF in normal and hypertrophied hearts of adiponectin knockout mice or wild-type mice with transverse aortic constriction (TAC). Then, we observed the effects of adiponectin on cardiac hypertrophy and HB-EGF signaling in cultured neonatal rat cardiomyocytes and whole hearts of adiponectin-null mice. The myocardial mRNA and protein expressions of adiponectin in the hypertrophied hearts were significantly downregulated, and the mRNA expression of adiponectin was inversely correlated with the heart-to-body weight ratio, BNP, and HB-EGF. The TAC-induced cardiac hypertrophy and EGF receptor (EGFR) activation in the adiponectin knockout mice were significantly greater than those in the wild-type mice. Furthermore, in vitro experiments revealed that adiponectin inhibited HB-EGF-stimulated protein synthesis, HB-EGF shedding, and EGFR phosphorylation. We conclude that the inhibition of HB-EGF mediated EGFR activation is one of the alternative mechanisms for the antihypertrophic action of adiponectin.
本研究旨在探讨脂联素在小鼠心脏中的抗心肌肥厚作用是否与 HB-EGF 信号的调节有关。我们测定了正常和脂联素敲除小鼠或经主动脉缩窄(TAC)处理的野生型小鼠的心脏中脂联素和脂联素受体、脑钠肽(BNP)和 HB-EGF 的心肌表达。然后,我们观察了脂联素对培养的新生大鼠心肌细胞和脂联素缺失小鼠的心脏整体中 HB-EGF 信号和心肌肥厚的影响。在肥厚的心脏中,脂联素的 mRNA 和蛋白表达显著下调,且脂联素的 mRNA 表达与心体比、BNP 和 HB-EGF 呈负相关。脂联素敲除小鼠的 TAC 诱导的心肌肥厚和表皮生长因子受体(EGFR)的激活明显大于野生型小鼠。此外,体外实验表明,脂联素抑制 HB-EGF 刺激的蛋白合成、HB-EGF 的脱落和 EGFR 磷酸化。我们的结论是,抑制 HB-EGF 介导的 EGFR 激活是脂联素抗心肌肥厚作用的另一种机制。