Effect of insulin deprivation on metabolism and metabolism-associated gene transcript levels of in vitro cultured human Sertoli cells

Biochim Biophys Acta. 2012 Feb;1820(2):84-9. doi: 10.1016/j.bbagen.2011.11.006. Epub 2011 Nov 20.

Abstract

Background: Sertoli 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.

Methods: hSC-enriched primary cultures were maintained in the absence/presence of insulin and metabolite variations were determined by (1)H-NMR. mRNA expression levels of glucose transporters (GLUT1, GLUT3), lactate dehydrogenase (LDHA) and monocarboxylate transporter (MCT4) were determined by RT-PCR.

Results: Insulin deprivation resulted in decreased lactate production and in decrease of glucose consumption that was completely reverted after 6h. 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 significance: This is the first report regarding the effect of insulin-deprivation on hSC metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine / biosynthesis
  • Cells, Cultured
  • Gene Expression Regulation* / drug effects
  • Glucose / metabolism
  • Glucose Transporter Type 3 / genetics
  • Glucose Transporter Type 3 / metabolism
  • Humans
  • Insulin / deficiency*
  • Insulin / pharmacology
  • L-Lactate Dehydrogenase / genetics
  • L-Lactate Dehydrogenase / metabolism
  • Lactic Acid / biosynthesis
  • Male
  • Monocarboxylic Acid Transporters / genetics
  • Monocarboxylic Acid Transporters / metabolism
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism
  • Pyruvates / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Sertoli Cells / enzymology
  • Sertoli Cells / metabolism*

Substances

  • Glucose Transporter Type 3
  • Insulin
  • Monocarboxylic Acid Transporters
  • Muscle Proteins
  • Pyruvates
  • RNA, Messenger
  • SLC16A4 protein, human
  • SLC2A3 protein, human
  • Lactic Acid
  • L-Lactate Dehydrogenase
  • Glucose
  • Alanine