Heme oxygenase-1 prevents heart against myocardial infarction by attenuating ischemic injury-induced cardiomyocytes senescence

EBioMedicine. 2019 Jan:39:59-68. doi: 10.1016/j.ebiom.2018.11.056. Epub 2018 Dec 5.

Abstract

Background: Cellular senescence is a stable cell-cycle arrest induced by telomere shortening and various types of cellular stress including oxidative stress, oncogene activation, DNA damage etc. Heme oxygenase-1 (HO-1) is an inducible stress-response protein that plays antioxidant and anti-apoptotic effects. However, the role and underlying mechanisms of HO-1 in cellular senescence in heart are largely unknown.

Methods: Echocardiography was employed to detect the effect of HO-1 on heart function in adult mice with myocardial infarction (MI) and aged mice. The senescence markers, p53, p16 and LaminB, were analyzed by western blot. The immunofluorescence and immunohistochemical staining were applied to analyze the expression level of p16. SA-β-Gal staining showed the level of cardiomyocyte senescence.

Findings: We found that hemin significantly induced the expression of HO-1, which notably suppressed cardiomyocyte senescence containing the secretion of senescence-associated secretory phenotype. Further studies showed that systemic HO-1 transgenic overexpression improved heart function by inhibiting aging-induced extracellular matrix deposition and fibrogenesis. More importantly, treatment of hemin improved heart function in MI mice. Furthermore, forced expression of HO-1 blunted cardiomyocyte senescence in natural aged mice and in primary cultured neonatal mouse cardiomyocytes.

Interpretation: Our study revealed that HO-1 improved heart function and attenuated cardiomyocyte senescence triggered by ischemic injury and aging. In addition, HO-1 induction alleviated H2O2-induced cardiomyocyte senescence. Finally, our study suggested a novel mechanism of HO-1 to play cardioprotective effect. FUND: This study was supported by the National Natural Science Foundation of China (81770284 to Hongli Shan); and the National Natural Science Foundation of China (81673425, 81872863 to Yuhong Zhou). The National Natural Science Foundation of China (81473213 to Chaoqian Xu). National Key R&D Program of China (2017YFC1307403 to Baofeng Yang), National Natural Science Foundation of China (81730012 to Baofeng Yang).

Keywords: Extracellular matrix; Heme oxygenase-1; Myocardial infarction; Senescence; Senescence-associated secretory phenotype.

MeSH terms

  • Aging / genetics
  • Aging / metabolism
  • Animals
  • Animals, Genetically Modified
  • Biomarkers / metabolism
  • Cells, Cultured
  • Cellular Senescence / drug effects
  • Disease Models, Animal
  • Extracellular Matrix / metabolism
  • Gene Expression Regulation / drug effects
  • Heme Oxygenase-1 / genetics*
  • Heme Oxygenase-1 / metabolism*
  • Hemin / administration & dosage*
  • Hemin / pharmacology
  • Hydrogen Peroxide / pharmacology
  • Male
  • Mice
  • Myocardial Infarction / genetics
  • Myocardial Infarction / metabolism
  • Myocardial Infarction / prevention & control*
  • Myocytes, Cardiac / cytology*
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism

Substances

  • Biomarkers
  • Hemin
  • Hydrogen Peroxide
  • HMOX1 protein, human
  • Heme Oxygenase-1