Deletion of protein tyrosine phosphatase 1B obliterates endoplasmic reticulum stress-induced myocardial dysfunction through regulation of autophagy

Biochim Biophys Acta Mol Basis Dis. 2017 Dec;1863(12):3060-3074. doi: 10.1016/j.bbadis.2017.09.015. Epub 2017 Sep 21.

Abstract

Endoplasmic reticulum (ER) stress has been demonstrated to prompt various cardiovascular risks although the underlying mechanism remains elusive. Protein tyrosine phosphatase-1B (PTP1B) serves as an essential negative regulator for insulin signaling. This study examined the role of PTP1B in ER stress-induced myocardial anomalies and underlying mechanism involved with a focus on autophagy. WT and PTP1B knockout mice were subjected to the ER stress inducer tunicamycin (1mg/kg). Cardiac function was evaluated with echocardiography and an Ion-Optix MyoCam system. Western blot analysis was used to monitor the levels of ER stress, autophagy and insulin signaling including insulin receptor substrate (IRS), tribbles homolog 3 (TRIB3), Atg5/7, p62 and LC3-II. Our results showed that ER stress resulted in compromised echocardiographic and cardiomyocyte contractile function, intracellular Ca2+ mishandling, ER stress, O2- production, apoptosis, the effects of which (with the exception of ER stress) were significantly attenuated or negated by PTP1B ablation. Levels of serine phosphorylation of IRS-1, TRIB3, Atg5/7, LC3B and the autophagy adaptor p62 were significantly upregulated while IRS-1 tyrosine phosphorylation was reduced by tunicamycin, the effect of which were obliterated by PTP1B ablation. In vitro study revealed that the autophagy inducer rapamycin and TRIB3 overexpression cancelled PTP1B ablation-offered beneficial effects on cardiomyocyte function or O2- production in murine cardiomyocytes or H9C2 myoblasts. Antioxidant or gene silencing of TRIB3 mimicked PTP1B ablation-induced protective effects. These findings collectively suggested that PTP1B ablation protects against ER stress-induced cardiac anomalies through regulation of autophagy.

Keywords: Autophagy; Cardiac function; ER stress; PTP1B; Tunicamycin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Autophagy / drug effects
  • Autophagy / physiology
  • Autophagy-Related Protein 5 / metabolism
  • Autophagy-Related Protein 7 / metabolism
  • Calcium / metabolism
  • Cardiomyopathies / enzymology*
  • Cardiomyopathies / metabolism
  • Cardiomyopathies / pathology
  • Cell Cycle Proteins / metabolism
  • Cell Line
  • Endoplasmic Reticulum Stress / drug effects
  • Endoplasmic Reticulum Stress / physiology*
  • Gene Knockout Techniques
  • Insulin Receptor Substrate Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microtubule-Associated Proteins / metabolism
  • Myoblasts / drug effects
  • Myoblasts / metabolism
  • Myoblasts / pathology
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / pathology
  • Oxygen / metabolism
  • Peptides / metabolism
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1 / deficiency*
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1 / genetics
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1 / metabolism
  • Signal Transduction
  • Sirolimus / pharmacology
  • Tunicamycin / pharmacology
  • Tyrosine / metabolism

Substances

  • Atg5 protein, mouse
  • Atg7 protein, mouse
  • Autophagy-Related Protein 5
  • Cell Cycle Proteins
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, mouse
  • Map1lc3b protein, mouse
  • Microtubule-Associated Proteins
  • P62 peptide
  • Peptides
  • TRB3 protein, mouse
  • Tunicamycin
  • Tyrosine
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1
  • Ptpn1 protein, mouse
  • Autophagy-Related Protein 7
  • Oxygen
  • Calcium
  • Sirolimus