Transformation of adult rat cardiac myocytes in primary culture

Exp Physiol. 2008 Mar;93(3):370-82. doi: 10.1113/expphysiol.2007.040659. Epub 2007 Dec 21.

Abstract

We characterized the morphological, electrical and mechanical alterations of cardiomyocytes in long-term cell culture. Morphometric parameters, sarcomere length, T-tubule density, cell capacitance, L-type calcium current (I(Ca,L)), inward rectifier potassium current (I(K1)), cytosolic calcium transients, action potential and contractile parameters of adult rat ventricular myocytes were determined on each day of 5 days in culture. We also analysed the health of the myocytes using an apoptotic/necrotic viability assay. The data show that myocytes undergo profound morphological and functional changes during culture. We observed a progressive reduction in the cell area (from 2502 +/- 70 microm(2) on day 0 to 1432 +/- 50 microm(2) on day 5), T-tubule density, systolic shortening (from 0.11 +/- 0.02 to 0.05 +/- 0.01 microm) and amplitude of calcium transients (from 1.54 +/- 0.19 to 0.67 +/- 0.19) over 5 days of culture. The negative force-frequency relationship, characteristic of rat myocardium, was maintained during the first 2 days but diminished thereafter. Cell capacitance (from 156 +/- 8 to 105 +/- 11 pF) and membrane currents were also reduced (I(Ca,L), from 3.98 +/- 0.39 to 2.12 +/- 0.37 pA pF; and I(K1), from 34.34p +/- 2.31 to 18.00 +/- 5.97 pA pF(-1)). We observed progressive depolarization of the resting membrane potential during culture (from 77.3 +/- 2.5 to 34.2 +/- 5.9 mV) and, consequently, action potential morphology was profoundly altered as well. The results of the viability assays indicate that these alterations could not be attributed to either apoptosis or necrosis but are rather an adaptation to the culture conditions over time.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological*
  • Animals
  • Calcium Channels, L-Type / metabolism
  • Calcium Signaling
  • Cardiac Pacing, Artificial
  • Cell Culture Techniques*
  • Cell Shape
  • Cell Size
  • Cell Survival
  • Cells, Cultured
  • Electric Capacitance
  • Membrane Potentials
  • Myocardial Contraction
  • Myocytes, Cardiac / metabolism*
  • Myocytes, Cardiac / pathology*
  • Potassium / metabolism
  • Potassium Channels, Inwardly Rectifying / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reproducibility of Results
  • Sarcolemma / metabolism
  • Sarcolemma / pathology
  • Sarcomeres / metabolism
  • Sarcomeres / pathology
  • Time Factors

Substances

  • Calcium Channels, L-Type
  • Potassium Channels, Inwardly Rectifying
  • Potassium