Decreased expression of insulin-sensitive glucose transporter mRNA (GLUT-4) in adipose tissue of non-insulin-dependent diabetic and obese patients: evaluation by a simplified quantitative PCR assay

J Endocrinol Invest. 1994 Oct;17(9):709-15. doi: 10.1007/BF03347765.

Abstract

Impaired cellular uptake and utilization of glucose is the hallmark of non-insulin-dependent-diabetes (NIDDM). We have developed a quantitative assay to probe the expression of glucose-transporter genes in tissues derived from patients with NIDDM. Using the polymerase chain reaction (PCR), we assessed levels of expression of the insulin responsive glucose transporter GLUT-4 in adipose tissue of patients with NIDDM and in obese patients. We report that expression of GLUT-4 is reduced in NIDDM and in obesity associated with hyperinsulinemia and insulin resistance. These results suggest that reduction of GLUT-4 levels in the adipose cell plays an important role in the pathogenesis of insulin resistance, an early feature of NIDDM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / chemistry
  • Adipose Tissue / metabolism*
  • Adipose Tissue / physiology
  • Base Sequence
  • Diabetes Mellitus, Type 2 / genetics
  • Diabetes Mellitus, Type 2 / metabolism*
  • Diabetes Mellitus, Type 2 / physiopathology
  • Female
  • Gene Expression
  • Glucose Transporter Type 4
  • Humans
  • Insulin Resistance / physiology
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Monosaccharide Transport Proteins / genetics*
  • Monosaccharide Transport Proteins / metabolism
  • Muscle Proteins*
  • Obesity / genetics
  • Obesity / metabolism*
  • Obesity / physiopathology
  • Oligonucleotides / analysis
  • Oligonucleotides / chemistry
  • Oligonucleotides / genetics
  • Polymerase Chain Reaction / methods
  • RNA, Messenger / analysis*
  • RNA, Messenger / genetics

Substances

  • Glucose Transporter Type 4
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • Oligonucleotides
  • RNA, Messenger
  • SLC2A4 protein, human