Human adipose tissue hormone-sensitive lipase: identification and comparison with other species

Biochim Biophys Acta. 1989 Nov 28;1006(2):193-7. doi: 10.1016/0005-2760(89)90195-1.

Abstract

The mRNA for human hormone-sensitive lipase (HSL) was identified using Northern blot analysis and a cDNA-probe for rat HSL. As in the rat, human adipose tissue expresses a single mRNA species of 3.3 kb. Using Western blotting with a polyclonal rabbit antibody towards rat adipose tissue HSL, the corresponding enzyme in human adipose tissue was identified with an apparent 88 kDa polypeptide, thus slightly larger than the rat and bovine 84 kDa, and the mouse and guinea-pig 82 kDa species. Additional evidence for the identification was provided by the inhibition of HSL diacylglycerol lipase activity by the anti-rat HSL antibody, and by NaF, DFP and Hg2+, known inhibitors of HSL. The concentration of the enzyme, as reflected by its activity per g tissue and the specific activity was about two thirds of that in the rat adipose tissue (200 g rats). The identification of the human enzyme protein made it possible to directly demonstrate its phosphorylation by cAMP-dependent protein kinase, thus extending the previous report regarding activation of the lipase with this kinase and ATP-Mg2+ in human adipose tissue extracts (Khoo, J.C., Aquino, A.A. and Steinberg, D. (1974) J. Clin. Invest. 53, 1124-1131).

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / enzymology*
  • Adult
  • Animals
  • Blotting, Western
  • Cattle
  • Cyclic AMP / pharmacology
  • DNA Probes
  • Female
  • Guinea Pigs
  • Hormones / pharmacology*
  • Humans
  • Male
  • Mice
  • Middle Aged
  • Molecular Weight
  • Nucleic Acid Hybridization
  • Phosphorylation
  • Protein Kinases / metabolism
  • RNA, Messenger / analysis
  • Rats
  • Sterol Esterase / analysis*
  • Sterol Esterase / genetics
  • Sterol Esterase / metabolism

Substances

  • DNA Probes
  • Hormones
  • RNA, Messenger
  • Cyclic AMP
  • Protein Kinases
  • Sterol Esterase