Decreased expression of apM1 in omental and subcutaneous adipose tissue of humans with type 2 diabetes

Int J Exp Diabetes Res. 2000;1(2):81-8. doi: 10.1155/edr.2000.81.

Abstract

We have screened a subtracted cDNA library in order to identify differentially expressed genes in omental adipose tissue of human patients with Type 2 diabetes. One clone (#1738) showed a marked reduction in omental adipose tissue from patients with Type 2 diabetes. Sequencing and BLAST analysis revealed clone #1738 was the adipocyte-specific secreted protein gene apM1 (synonyms ACRP30, AdipoQ, GBP28). Consistent with the murine orthologue, apM1 mRNA was expressed in cultured human adipocytes and not in preadipocytes. Using RT-PCR we confirmed that apM1 mRNA levels were significantly reduced in omental adipose tissue of obese patients with Type 2 diabetes compared with lean and obese normoglycemic subjects. Although less pronounced, apM1 mRNA levels were reduced in subcutaneous adipose tissue of Type 2 diabetic patients. Whereas the biological function of apM1 is presently unknown, the tissue specific expression, structural similarities to TNFalpha, and the dysregulated expression observed in obese Type 2 diabetic patients suggest that this factor may play a role in the pathogenesis of insulin resistance and Type 2 diabetes.

MeSH terms

  • Adiponectin
  • Adipose Tissue / metabolism*
  • Adult
  • Blood Glucose / analysis
  • Body Mass Index
  • Collagen / genetics
  • Diabetes Mellitus / blood
  • Diabetes Mellitus / genetics*
  • Diabetes Mellitus / metabolism
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetes Mellitus, Type 2 / metabolism
  • Fasting
  • Gene Library
  • Humans
  • Insulin / blood
  • Intercellular Signaling Peptides and Proteins*
  • Middle Aged
  • Obesity / blood
  • Obesity / genetics*
  • Obesity / metabolism
  • Omentum
  • Proteins / genetics*
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Skin
  • Thinness
  • Transcription, Genetic*

Substances

  • Adiponectin
  • Blood Glucose
  • Insulin
  • Intercellular Signaling Peptides and Proteins
  • Proteins
  • RNA, Messenger
  • Collagen