The aim of this study was to evaluate the effect of protein-tyrosine kinase (PTK) and protein tyrosine phosphatase (PTP) inhibitors on Ca2+ channels in GH(3) cells, The activity of Ca2+ channels was monitored either by single-cell microfluorometry or by the whole cell configuration of the patch-clamp technique, Genistein (20-200 mu M) and herbimycin A (1-15 mu M) inhibited [Ca2+](i) rise induced either by 55 mM K+ or 10 mu M Bay K 8644, In addition, genistein and lavendustin A inhibited whole-cell Ba2+ currents, By contrast, daidzein, a genistein analogue devoid of PTK inhibitory properties, did not modify Ca2+ channel activity. The inhibitory action of genistein on the [Ca2+](i) increase was completely counteracted by the PTP inhibitor vanadate (100 mu M). Furthermore, vanadate alone potentiated [Ca2+](i) response to both 55 mM K+ and 10 mu M Bay K 8644. The possibility that genistein could decrease the [Ca2+](i) elevation by enhancing Ca2+ removal from the cytosol seems unlikely since genistein also reduced the increase in fura-2 fluorescence ratio induced by Ba2+, a cation that enters into the cells through Ca2+ channels but cannot be pumped out by Ca2+ extrusion mechanisms, Finally, in unstimulated GH(3) cells, genistein caused a decline of [Ca2+](i) and the disappearance of [Ca2+](i) oscillations, whereas vanadate induced an increase of [Ca2+](i) and the appearance of [Ca2+](i) oscillations in otherwise non-oscillating cells. The present results suggest that in GH(3) cells PTK activation causes an increase of L-type Ca2+ channel function, whereas PTPs exert an inhibitory role.

Protein-tyrosine kinases activate while protein-tyrosine phosphatases inhibit L-type calcium channel activity in pituitary GH(3) cells

TAGLIALATELA, Maurizio;
1996-01-01

Abstract

The aim of this study was to evaluate the effect of protein-tyrosine kinase (PTK) and protein tyrosine phosphatase (PTP) inhibitors on Ca2+ channels in GH(3) cells, The activity of Ca2+ channels was monitored either by single-cell microfluorometry or by the whole cell configuration of the patch-clamp technique, Genistein (20-200 mu M) and herbimycin A (1-15 mu M) inhibited [Ca2+](i) rise induced either by 55 mM K+ or 10 mu M Bay K 8644, In addition, genistein and lavendustin A inhibited whole-cell Ba2+ currents, By contrast, daidzein, a genistein analogue devoid of PTK inhibitory properties, did not modify Ca2+ channel activity. The inhibitory action of genistein on the [Ca2+](i) increase was completely counteracted by the PTP inhibitor vanadate (100 mu M). Furthermore, vanadate alone potentiated [Ca2+](i) response to both 55 mM K+ and 10 mu M Bay K 8644. The possibility that genistein could decrease the [Ca2+](i) elevation by enhancing Ca2+ removal from the cytosol seems unlikely since genistein also reduced the increase in fura-2 fluorescence ratio induced by Ba2+, a cation that enters into the cells through Ca2+ channels but cannot be pumped out by Ca2+ extrusion mechanisms, Finally, in unstimulated GH(3) cells, genistein caused a decline of [Ca2+](i) and the disappearance of [Ca2+](i) oscillations, whereas vanadate induced an increase of [Ca2+](i) and the appearance of [Ca2+](i) oscillations in otherwise non-oscillating cells. The present results suggest that in GH(3) cells PTK activation causes an increase of L-type Ca2+ channel function, whereas PTPs exert an inhibitory role.
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11695/7466
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? 86
social impact