Purinergic agonists stimulate the secretion of endothelin-1 in rat thyroid FRTL-5 cells

J Cell Physiol. 1996 Dec;169(3):538-43. doi: 10.1002/(SICI)1097-4652(199612)169:3<538::AID-JCP14>3.0.CO;2-1.

Abstract

The aim of the present study was to investigate the mechanisms regulating endothelin-1 (ET-1) secretion in rat thyroid FRTL-5 cells. ET-1 was found to be secreted after stimulation with adenosine and ATP. The release of ET-1 was sensitive to pertussis toxin, indicating a role of G-proteins in the stimulus-secretion coupling. The stimulation evoked by ATP or adenosine was inhibited by the P1-receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX), and in the presence of adenosine deaminase the adenosine- and ATP-mediated ET-1 secretion was abolished. These evidences suggest a role of a P1-adenosine receptor in the secretion of ET-1. Increasing cyclic AMP with forskolin decreased the adenosine-mediated secretion. In addition, the intracellular calcium chelator BAPTA or inhibition of calcium entry with Ni2+ prevented the response. Protein kinase C (PKC) is also partly involved in ET-1 secretion in FRTL-5 cells. Activation of PKC with the phorbol ester phorbol 12-myristate 13-acetate (PMA) stimulated the secretion of ET-1 in a time- and dose-dependent manner. Furthermore, downregulation of PKC decreased the secretion of ET-1 stimulated by adenosine. In conclusion, ET-1 secretion in FRTL-5 cells is stimulated via a pertussis toxin-sensitive P1-receptor pathway which is modulated by several signal transduction mechanisms including cAMP, Ca2+, and PKC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / pharmacology*
  • Adenosine Deaminase / pharmacology
  • Adenosine Triphosphate / pharmacology*
  • Animals
  • Calcium / physiology
  • Cell Line
  • Cyclic AMP / physiology
  • Cyclic GMP / physiology
  • Endothelin-1 / metabolism*
  • Enzyme Activation
  • Nitric Oxide / physiology
  • Protein Kinase C / physiology
  • Purinergic P1 Receptor Agonists*
  • Rats
  • Receptors, Purinergic P1 / physiology
  • Secretory Rate / drug effects
  • Signal Transduction
  • Thyroid Gland
  • Xanthines / pharmacology

Substances

  • Endothelin-1
  • Purinergic P1 Receptor Agonists
  • Receptors, Purinergic P1
  • Xanthines
  • Nitric Oxide
  • Adenosine Triphosphate
  • 1,3-dipropyl-8-cyclopentylxanthine
  • Cyclic AMP
  • Protein Kinase C
  • Adenosine Deaminase
  • Cyclic GMP
  • Adenosine
  • Calcium