A cytoplasmic factor, calpastatin and ATP together reverse run-down of Ca2+ channel activity in guinea-pig heart

J Physiol. 1999 Feb 1;514 ( Pt 3)(Pt 3):687-99. doi: 10.1111/j.1469-7793.1999.687ad.x.

Abstract

1. The cytoplasmic extract of bovine heart was separated into four fractions by gel filtration: H (molecular mass > 300 kDa), P (250-300 kDa), L1 (180-250 kDa) and L2 (< 180 kDa). The effects of these fractions on the run-down of L-type Ca2+ channel activity were investigated in guinea-pig ventricular myocytes. 2. After run-down induced by inside-out patch formation, Ca2+ channel activity was restored by P or H (+ 3 mM ATP) to 7.5 and 5.8 % of that in the cell-attached mode, respectively, but to as high as 86 % by P + H + ATP. 3. The reversal of run-down brought about by the P fraction was mimicked by calpastatin. 4. The restorative effect of calpastatin + ATP showed a biphasic time course: 38 % in the early transient phase and 11 % in the late phase. However, calpastatin + H + ATP showed a sustained effect: 66 % in the early transient phase, and 87 % in the late phase. 5. The effective component of the H fraction showed a protein-like nature: heat and trypsin sensitivity. 6. The activities of cAMP-dependent protein kinase, casein kinase I, casein kinase II, protein tyrosine kinase, protein serine/threonine or tyrosine phosphatases were measured. However, these kinases and phosphatases were not confirmed as the effective component of cytoplasm or the H fraction. 7. Run-down was not prevented by 2 microM phalloidin or 2 microM paclitaxel, suggesting that neither actin filaments nor microtubules are directly involved in the run-down. 8. Our results support the view that the basal activity of the Ca2+ channel is maintained by at least three factors: a protein-like factor in the H fraction, calpastatin, and ATP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / pharmacology
  • Adenosine Triphosphate / physiology*
  • Animals
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Calcium Channels / metabolism*
  • Calcium-Binding Proteins / physiology*
  • Cattle
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Cysteine Proteinase Inhibitors / physiology*
  • Cytoplasm / metabolism
  • Electric Stimulation
  • Guinea Pigs
  • Heart / physiology*
  • In Vitro Techniques
  • Membrane Potentials / physiology
  • Myocardium / metabolism*
  • Paclitaxel / pharmacology
  • Patch-Clamp Techniques
  • Tissue Extracts / pharmacology

Substances

  • Antineoplastic Agents, Phytogenic
  • Calcium Channels
  • Calcium-Binding Proteins
  • Cysteine Proteinase Inhibitors
  • Tissue Extracts
  • calpastatin
  • Adenosine Triphosphate
  • Cyclic AMP-Dependent Protein Kinases
  • Paclitaxel