کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1947785 | 1054647 | 2012 | 6 صفحه PDF | دانلود رایگان |

BackgroundSertoli cells metabolize glucose producing lactate for developing germ cells. As insulin regulates glucose uptake and its disturbance/insensitivity is associated with diabetes mellitus, we aimed to determine the effect of insulin deprivation in human Sertoli cell (hSC) metabolism and metabolism-associated gene expression.MethodshSC-enriched primary cultures were maintained in the absence/presence of insulin and metabolite variations were determined by 1H-NMR. mRNA expression levels of glucose transporters (GLUT1, GLUT3), lactate dehydrogenase (LDHA) and monocarboxylate transporter (MCT4) were determined by RT-PCR.ResultsInsulin deprivation resulted in decreased lactate production and in decrease of glucose consumption that was completely reverted after 6 h. Cells of both groups consumed similar amounts of glucose. In insulin-deprived cells, transcript levels of genes associated to lactate metabolism (LDHA and MCT4) were decreased. Transcript levels of genes involved in glucose uptake exhibited a divergent variation: GLUT3 levels were decreased while GLUT1 levels increased.Insulin-deprived hSCs presented: 1) altered glucose consumption and lactate secretion; 2) altered expression of metabolism-associated genes involved in lactate production and export; 3) an adaptation of glucose uptake by modulating the expression of GLUT1 and GLUT3.General significanceThis is the first report regarding the effect of insulin-deprivation on hSC metabolism.
Figure optionsDownload high-quality image (50 K)Download as PowerPoint slideHighlights
► The first hours of insulin deprivation are critical in hSCs in vitro.
► Insulin deprivation affects glucose uptake and lactate production/export.
► Insulin-deprived hSCs present altered expression of metabolism-associated genes.
► GLUT1 and GLUT3 expression levels are modulated by insulin-deprivation in hSCs.
Journal: Biochimica et Biophysica Acta (BBA) - General Subjects - Volume 1820, Issue 2, February 2012, Pages 84–89