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PMID: 10634941 Published · ppublish English Journal Article

The lipolytic stimulation of 3T3-L1 adipocytes promotes the translocation of hormone-sensitive lipase to the surfaces of lipid storage droplets.

Biochimica et biophysica acta ·Vol. 1483 ·No. 2 ·2000-01-17 ·Pages 251-62

Brasaemle DL, Levin DM, Adler-Wailes DC, Londos C

Abstract

Hormone-sensitive lipase catalyzes the rate-limiting step in the release of fatty acids from triacylglycerol-rich lipid storage droplets of adipocytes, which contain the body's major energy reserves. Hormonal stimulation of cAMP formation and the activation of cAMP-dependent protein kinase leads to the phosphorylation of hormone-sensitive lipase and a large increase in lipolysis in adipocytes. By contrast, phosphorylation of hormone-sensitive lipase by the kinase in vitro results in a comparatively minor increase in catalytic activity. In this study, we investigate the basis for this discrepancy by using immunofluorescence microscopy to locate hormone-sensitive lipase in lipolytically stimulated and unstimulated 3T3-L1 adipocytes. In unstimulated cells, hormone-sensitive lipase is diffusely distributed throughout the cytosol. Upon stimulation of cells with the beta-adrenergic receptor agonist, isoproterenol, hormone-sensitive lipase translocates from the cytosol to the surfaces of intracellular lipid droplets concomitant with the onset of lipolysis, as measured by the release of glycerol to the culture medium. Both hormone-sensitive lipase translocation and lipolysis are reversed by the incubation of cells with the beta-adrenergic receptor antagonist, propranolol. The treatment of cells with cycloheximide fails to inhibit lipase translocation or lipolysis, indicating that the synthesis of nascent proteins is not required. Cytochalasin D and nocodazole used singly and in combination also failed to have a major effect, thus suggesting that the polymerization of microfilaments and microtubules and the formation of intermediate filament networks is unnecessary. Hormone-sensitive lipase translocation and lipolysis were inhibited by N-ethylmaleimide and a combination of deoxyglucose and sodium azide. We propose that the major consequence of the phosphorylation of hormone-sensitive lipase following the lipolytic stimulation of adipocytes is the translocation of the lipase from the cytosol to the surfaces of lipid storage droplets.

MeSH Terms
3T3 Cells Adenosine Triphosphate/metabolism Adipocytes/drug effects,enzymology Animals Biological Transport/drug effects Cell Differentiation Cyclic AMP/analogs & derivatives Cytoskeleton/drug effects Cytosol/enzymology Enzyme Activation Ethylmaleimide/pharmacology Isoproterenol/pharmacology Lipolysis/drug effects Mice Microscopy, Fluorescence Propranolol/pharmacology Sterol Esterase/analysis Surface Properties
Chemicals
Adenosine Triphosphate Propranolol Cyclic AMP Sterol Esterase Isoproterenol Ethylmaleimide
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Brasaemle D L
Laboratory of Cellular and Developmental Biology, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda 20892-2715, USA.
Levin D M
Adler-Wailes D C
Londos C
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
2000-01-17
Pages
251-62
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
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