Aging aggravates heterogeneities in cell-size and stress-intolerance of cardiac ventricular myocytes

Exp Gerontol. 2006 May;41(5):489-96. doi: 10.1016/j.exger.2006.03.003. Epub 2006 Apr 18.

Abstract

Rationale: Heterogeneity of ventricular myocytes from old murine hearts was tested in regard to cell volume and tolerance to stress induced by ROS generated by photoactivation of tetramethylrhodamine methylester.

Results: During repetitive linescans, ROS generated 'scars' of depolarized mitochondria. All young and 60% of old myocytes had type1 scars that were small and remained stable with time. Forty percent cells from old hearts responded with type2 scars that were wide and expanded with time. Depolarization of individual mitochondria was characterized by its half decay time. HDT was 6.9s in young mice (type1 mitochondria). HDT was 5.6s in old mice due to a 30% population of mitochondria with reduced ROS-tolerance (type2, HDT=3.0 s). Type1 and type2 mitochondria did not coexist in the same cell, however, in the same old heart (different myocytes). In a different set of myocytes the volumes were measured to be larger (83+/-29 pl) and more heterogeneous than in young myocytes (49+/-13 pl).

Conclusion: Hearts of old mice contain a subpopulation of myocytes with reduced mitochondrial stress-tolerance that is attributed to an age-dependent reduction of cellular ROS defence capacity. We discuss how heterogeneities in stress-tolerance and cell volume could be causally linked.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / pathology
  • Animals
  • Cell Size*
  • Cells, Cultured
  • Cellular Senescence / physiology*
  • Male
  • Membrane Potential, Mitochondrial / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria, Heart / physiology
  • Myocytes, Cardiac / cytology*
  • Myocytes, Cardiac / physiology
  • Oxidative Stress / physiology*
  • Reactive Oxygen Species / metabolism

Substances

  • Reactive Oxygen Species