Alteration of the functional activity of Gs protein in thyrotropin-desensitized pig thyroid cells

Mol Cell Endocrinol. 1991 Feb;75(2):123-31. doi: 10.1016/0303-7207(91)90226-i.

Abstract

Changes in the sensitivity of adenylyl cyclase observed in pig thyroid cells cultured 2 days in the presence of thyroid-stimulating hormone (TSH) or forskolin were assessed by examining the properties of Gs protein. Chronic treatment of thyroid cells with various concentrations of TSH (0.01-1 mU/ml) or forskolin (0.1-10 microM) increased the response of adenylyl cyclase to a further stimulation by forskolin or NaF + AlCl3 ([AlF4]-). In contrast, the enzyme activation promoted by guanosine 5'-(beta,gamma-imido) triphosphate (Gpp(NH)p) was markedly affected. There was a significant increase in adenylyl cyclase activation by Gpp(NH)p in membranes from cells treated with low concentrations of TSH (less than or equal to 0.1 mU/ml) or forskolin (less than or equal to 1 microM) but a significant decrease in membranes from cells cultured with a higher concentration of TSH (1 mU/ml) or forskolin (10 microM). This decrease in Gpp(NH)p-stimulated adenylyl cyclase activity was mimicked by 8-bromo-cAMP but not by 1,9-dideoxyforskolin, a forskolin analogue which has lost its ability to activate adenylyl cyclase. There was a good correlation with the ability of Gs protein to be ADP-ribosylated by cholera toxin: labeling of Gs protein decreased following chronic treatment of thyroid cells with TSH (1 mU/ml) or forskolin (10 microM). In contrast, under the same experimental culture conditions a slight but significant increase in the quantity of Gs subunits was observed by immunoblotting analysis.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 8-Bromo Cyclic Adenosine Monophosphate / pharmacology
  • Adenosine Diphosphate Ribose / metabolism
  • Adenylyl Cyclases / metabolism*
  • Animals
  • Cells, Cultured
  • Cholera Toxin / pharmacology
  • Colforsin / analogs & derivatives
  • Colforsin / pharmacology
  • Cyclic AMP / metabolism*
  • Enzyme Activation / drug effects
  • GTP-Binding Proteins / metabolism*
  • Second Messenger Systems / drug effects
  • Swine / metabolism
  • Thyroid Gland / cytology
  • Thyroid Gland / metabolism*
  • Thyrotropin / pharmacology*

Substances

  • Colforsin
  • Adenosine Diphosphate Ribose
  • 8-Bromo Cyclic Adenosine Monophosphate
  • Thyrotropin
  • Cholera Toxin
  • Cyclic AMP
  • GTP-Binding Proteins
  • Adenylyl Cyclases
  • 1,9-dideoxyforskolin