Mammalian target of rapamycin controls glucose consumption and redox balance in human Sertoli cells

• Tipo: Artigo em Revista Científica Internacional
• Data: 2016

Autores

Jesus, TT (Autor) Outra; Oliveira, PF (Autor) ICBAS; Silva, J (Autor) Outra; barros, a (Autor) FMUP; Ferreira, R (Autor) Outra; sousa, m (Autor) ICBAS; Cheng, CY (Autor) Outra; Silva, BM (Autor) Outra; Alves, MG (Autor) Outra

Revista

Título: Fertility and Sterility

Vol. 105

Páginas: 825-+

ISSN: 0015-0282

Editora: Elsevier

Indexação

ISI Web of Knowledge - 30 Citações

Scopus - 34 Citações

Outras Informações

ID Authenticus: P-00K-8CW

DOI: 10.1016/j.fertnstert.2015.11.032

Abstract (EN): Objective: To study the role of mammalian target of rapamycin (mTOR) in the regulation of human Sertoli cell (hSC) metabolism, mitochondrial activity, and oxidative stress. Design: Experimental study. Setting: University research center and private assisted reproductive technology centers. Patient(s): Six men with anejaculation (psychological, vascular, neurologic) and conserved spermatogenesis. Intervention(s): Testicular biopsies were used from patients under treatment for recovery of male gametes. Primary hSCs cultures were established from each biopsy and divided into a control group and one treated with rapamycin, the inhibitor of mTOR, for 24 hours. Main Outcome Measure(s): Cytotoxicity of hSCs to rapamycin was evaluated by sulforhodamine B assay. The glycolytic profile of hSCs was assessed by proton nuclear magnetic resonance and by studying protein expression of key glycolysis-related transporters and enzymes. Expression of mitochondrial complexes and citrate synthase activity were determined. Protein carbonylation, nitration, lipid peroxidation, and sulfhydryl protein group contents were quantified. The mTOR signaling pathway was studied. Result(s): Rapamycin increased glucose consumption by hSCs, maintaining lactate production. Alanine production by rapamycin-exposed hSCs was affected, resulting in an unbalanced intracellular redox state. Rapamycin-exposed hSCs had decreased expression of mitochondrial complex III and increased lipid peroxidation, whereas other oxidative stress markers were unaltered. Treatment of hSCs with rapamycin down-regulated phospho-mTOR (Ser-2448) levels, illustrating an effective partial inhibition of mTORC1. Protein levels of downstream signaling molecule p-4E-BP1 were not altered, suggesting that during treatment it became rephosphorylated. Conclusion(s): We show that mTOR regulates the nutritional support of spermatogenesis by hSCs and redox balance in these cells. (C) 2016 by American Society for Reproductive Medicine.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 12