info:eu-repo/semantics/article
Interleukin-1ß regulates nitric oxide production and gamma-glutamyltranspeptidase activity in Sertoli cells
Fecha
2000-12Registro en:
Meroni, Silvina Beatriz; Suburo, Angela Maria; Cigorraga, Selva Beatriz; Interleukin-1ß regulates nitric oxide production and gamma-glutamyltranspeptidase activity in Sertoli cells; American Society of Andrology; Journal of Andrology; 21; 6; 12-2000; 855-861
0196-3635
CONICET Digital
CONICET
Autor
Meroni, Silvina Beatriz
Suburo, Angela Maria
Cigorraga, Selva Beatriz
Resumen
Several cytokines have been involved in the regulation of Sertoli cell  function. Further investigations are required to elucidate the role of  interleukin-1beta (IL1beta) in Sertoli cell physiology. Twenty-day-old  rat Sertoli cell cultures were used to investigate a possible role of  IL1beta in the regulation of gamma-glutamyl transpeptidase (gammaGTP)  and to elucidate the signaling pathway utilized by this cytokine.  GammaGTP is a membrane-bound enzyme that has been involved in amino  acid transport across the plasma membrane and in protection from  oxidative stress through its importance in the regulation of  glutathione levels. Previous studies suggested that IL1beta stimulates  NO biosynthesis in other cell types. Therefore, we investigated whether  IL1beta modified the level of nitrite, a stable metabolite of NO, in  Sertoli cells. Dose-response curves to IL1beta for gammaGTP activity  and nitrite production were observed. The increments observed in  gammaGTP activity and nitrite production were partially and completely  blocked by simultaneous treatment with the NO synthase inhibitor  aminoguanidine. Treatment of Sertoli cell cultures with the NO donors  sodium nitroprusside and S-nitroso-N-acetylpenicillamine resulted in an  increase in gammaGTP activity. The presence of neural, endothelial, and  inducible isoforms of NO synthase (NOS) was investigated by a  immunohistochemical technique using specific antibodies. The 2  constitutive isoforms were present under basal conditions, and the  inducible protein appeared in IL1beta-treated cultures. Finally,  translocation of NF-kappaB p65 subunit to the nucleus in  IL1beta-treated cultures was observed. These findings suggest that the  action of IL1beta on Sertoli cell gammaGTP activity is partially  mediated via activation of NF-kappaB and increments in iNOS and  cellular production of NO.