Desensitization of calcium messenger system in parathyroid hormone-stimulated opossum kidney cells

Am J Physiol. 1993 Jun;264(6 Pt 1):E918-24. doi: 10.1152/ajpendo.1993.264.6.E918.

Abstract

We have studied the desensitization of the calcium message system to parathyroid hormone (PTH) by monitoring intracellular calcium concentration ([Ca2+]i) in an opossum kidney cell line (OKP). PTH (10(-7) M) caused a transient increase in [Ca2+]i, with an average peak height of 48.7 +/- 4.7% above baseline (n = 32). Cells stimulated with either 10(-7) or 10(-8) M PTH did not respond to a second challenge with a maximal dose (10(-7) M) of the hormone, whereas lower concentrations of PTH (10(-9) M and 10(-10) M) only partially desensitized the cells, since a [Ca2+]i transient of smaller amplitude (12.7 +/- 2.1 and 40.6 +/- 6.2% above baseline, respectively) was observed with a second stimulation. Desensitization developed within 5 min of initial hormone exposure, when PTH receptor binding was not significantly decreased. Maximal reduction of PTH binding sites (37.0 +/- 1.4%) was achieved only after 2 h. Partial desensitization was reproduced by 10(-9) M phorbol 12-myristate 13-acetate (PMA) but not by dibutyryladenosine 3',5'-cyclic monophosphate, and it was blocked by staurosporine. However, staurosporine had no effect on the complete desensitization induced by high doses of PTH. At 10(-9) M, PTH also caused a time-dependent desensitization of the adenosine 3',5'-cyclic monophosphate (cAMP) response, with maximal inhibition achieved after 2 h. PMA also decreased the cAMP response to PTH, but its inhibitory effect was less potent than that of 10(-9) M PTH. Therefore PTH induces a dose-dependent homologous desensitization of the Ca2+ message system in OKP cells, independent of receptor occupancy.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alkaloids / pharmacology
  • Animals
  • Calcium / metabolism
  • Calcium / physiology*
  • Clone Cells
  • Cyclic AMP / metabolism
  • Dose-Response Relationship, Drug
  • Electrophysiology
  • Intracellular Membranes / metabolism
  • Kidney / cytology
  • Kidney / drug effects*
  • Kidney / physiology*
  • Opossums
  • Osmolar Concentration
  • Parathyroid Hormone / metabolism
  • Parathyroid Hormone / pharmacology*
  • Protein Kinase C / antagonists & inhibitors
  • Second Messenger Systems*
  • Staurosporine
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Alkaloids
  • Parathyroid Hormone
  • Cyclic AMP
  • Protein Kinase C
  • Staurosporine
  • Tetradecanoylphorbol Acetate
  • Calcium