Subspace-located catalase prevents membrane degradation and dyssynchronization of local calcium release in adult cardiomyocytes

Free Radic Biol Med. 2025 Dec 16:241:807-817. doi: 10.1016/j.freeradbiomed.2025.10.255. Epub 2025 Oct 10.

Abstract

Catalase, a canonical antioxidant enzyme, has been shown to prevent maladaptive oxidative damage and protect against aging-associated deterioration of cellular functions. In cardiac tissue, catalase protects cardiac myocytes against a variety of pathological changes by maintaining normal contractile function. Here we elucidated how catalase can protect cardiomyocyte excitation-contraction (EC) coupling we focused on exploring the subcellular location and specific effects of catalase in cardiomyocytes. To determine the effects of catalase on cardiomyocyte EC-coupling, we used adenoviral overexpression and pharmacological inhibition of catalase with 3AT in cultured adult mouse ventricular myocytes combined with detailed characterization of Ca2+ signaling. We found that endogenous catalase co-localizes with RyRs in the subspace between the junctional sarcoplasmic reticulum (SR) and t-tubules. When virally overexpressed, catalase increases the ROS scavenging capacity of myocytes and enhances Ca2+-release by increasing synchronization of local Ca2+-release. To improve Ca2+-release, catalase acts to prevent membrane peroxidation and prevents degradation of t-tubule structures. Both the functional and structural effects of catalase were reversed by catalase inhibition with 3AT. The effect of catalase on Ca2+-release was more pronounced in cardiomyocytes isolated from transverse aortic constriction-operated, hypertrophied mouse hearts. Overall, our data suggest that catalase located to the subspace has a specific role in stabilizing and protecting Ca2+-release structures from degradation in conditions associated with increased oxidative stress.

Keywords: Antioxidant; Calcium release unit; EC-Coupling; ROS; T-tubule.

MeSH terms

  • Animals
  • Calcium Signaling
  • Calcium* / metabolism
  • Catalase* / antagonists & inhibitors
  • Catalase* / genetics
  • Catalase* / metabolism
  • Cells, Cultured
  • Excitation Contraction Coupling
  • Heart Ventricles
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myocytes, Cardiac* / metabolism
  • Oxidative Stress
  • Reactive Oxygen Species / metabolism
  • Ryanodine Receptor Calcium Release Channel / genetics
  • Ryanodine Receptor Calcium Release Channel / metabolism
  • Sarcoplasmic Reticulum / metabolism

Substances

  • Catalase
  • Calcium
  • Ryanodine Receptor Calcium Release Channel
  • Reactive Oxygen Species