Acute Induction of Translocon-Mediated Ca2+ Leak Protects Cardiomyocytes Against Ischemia/Reperfusion Injury

Cells. 2020 May 25;9(5):1319. doi: 10.3390/cells9051319.

Abstract

During myocardial infarction, dysregulation of Ca2+ homeostasis between the reticulum, mitochondria, and cytosol occurs in cardiomyocytes and leads to cell death. Ca2+ leak channels are thought to be key regulators of the reticular Ca2+ homeostasis and cell survival. The present study aimed to determine whether a particular reticular Ca2+ leak channel, the translocon, also known as translocation channel, could be a relevant target against ischemia/reperfusion-mediated heart injury. To achieve this objective, we first used an intramyocardial adenoviral strategy to express biosensors in order to assess Ca2+ variations in freshly isolated adult mouse cardiomyocytes to show that translocon is a functional reticular Ca2+ leak channel. Interestingly, translocon activation by puromycin mobilized a ryanodine receptor (RyR)-independent reticular Ca2+ pool and did not affect the excitation-concentration coupling. Second, puromycin pretreatment decreased mitochondrial Ca2+ content and slowed down the mitochondrial permeability transition pore (mPTP) opening and the rate of cytosolic Ca2+ increase during hypoxia. Finally, this translocon pre-activation also protected cardiomyocytes after in vitro hypoxia reoxygenation and reduced infarct size in mice submitted to in vivo ischemia-reperfusion. Altogether, our report emphasizes the role of translocon in cardioprotection and highlights a new paradigm in cardioprotection by functionally uncoupling the RyR-dependent Ca2+ stores and translocon-dependent Ca2+ stores.

Keywords: Ca2+ leak channel; cardioprotection; ischemia-reperfusion; reticulum; translocon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Cardiotonic Agents / metabolism*
  • Excitation Contraction Coupling
  • Male
  • Mice, Inbred C57BL
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondrial Permeability Transition Pore / metabolism
  • Myocytes, Cardiac / metabolism*
  • Myocytes, Cardiac / pathology*
  • Puromycin / pharmacology
  • Reperfusion Injury / metabolism*
  • Reperfusion Injury / pathology*
  • Ryanodine Receptor Calcium Release Channel / metabolism
  • SEC Translocation Channels / metabolism*

Substances

  • Cardiotonic Agents
  • Mitochondrial Permeability Transition Pore
  • Ryanodine Receptor Calcium Release Channel
  • SEC Translocation Channels
  • Puromycin
  • Calcium