Regulation of FAT/CD36 gene expression: further evidence in support of a role of the protein in fatty acid binding/transport

Prostaglandins Leukot Essent Fatty Acids. 1997 Jul;57(1):17-21. doi: 10.1016/s0952-3278(97)90487-7.


Much biochemical evidence has implicated rat adipocyte CD36 (FAT) in membrane binding and transport of long-chain fatty acids (FA). Expression of the mRNA favored tissues with active FA metabolism and was upregulated in vivo with diabetes and with high fat feeding. In culture, CD36 mRNA was a strong marker of preadipocyte differentiation and was modulated by the same factors effective on mRNAs coding for other proteins involved in FA metabolism. In preadipocytes, long-chain FA or 2-bromopalmitate but not short-chain FA strongly induced CD36 mRNA within 8 h to an optimum within 24 h. Removal of the FA resulted in a decay of CD36 mRNA with a half life of about 12 h. In differentiated adipocytes, levels of CD36 mRNA were downregulated by the 3': 5'-cyclic adenosine monophosphate, cAMP, analog, 8-(4-chlorophenylthio) adenosine, 8-CPT, at concentrations of 1-100 microM. The effect, observed within 6 h, was optimal after 18 h and independent of the action of 8-CPT to mobilize FA. Regulation of CD36 expression by factors effective on expression of other proteins implicated in FA metabolism is consistent with its role in membrane FA transport.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adipocytes / metabolism*
  • Animals
  • Biological Transport
  • CD36 Antigens / genetics*
  • Cell Line
  • Cyclic AMP / pharmacology
  • Fatty Acids / metabolism*
  • Gene Expression Regulation* / drug effects
  • Kinetics
  • Membrane Glycoproteins / genetics*
  • Organic Anion Transporters*
  • RNA, Messenger / biosynthesis
  • Rats
  • Stem Cells / metabolism


  • CD36 Antigens
  • Fatty Acids
  • Membrane Glycoproteins
  • Organic Anion Transporters
  • RNA, Messenger
  • Cyclic AMP