16188906

pubmed:Citation

3

Hormone-sensitive lipase (HSL) is important for the degradation of triacylglycerol in adipose and muscle tissue, but the tissue-specific regulation of this enzyme is not fully understood. We investigated the effects of adrenergic stimulation and AMPK activation in vitro and in circumstances where AMPK activity and catecholamines are physiologically elevated in humans in vivo (during physical exercise) on HSL activity and phosphorylation at Ser(563) and Ser(660), the PKA regulatory sites, and Ser(565), the AMPK regulatory site. In human experiments, skeletal muscle, subcutaneous adipose and venous blood samples were obtained before, at 15 and 90 min during, and 120 min after exercise. Skeletal muscle HSL activity was increased by approximately 80% at 15 min compared with rest and returned to resting rates at the cessation of and 120 min after exercise. Consistent with changes in plasma epinephrine, skeletal muscle HSL Ser(563) and Ser(660) phosphorylation were increased by 27% at 15 min (P < 0.05), remained elevated at 90 min, and returned to preexercise values postexercise. Skeletal muscle HSL Ser(565) phosphorylation and AMPK signaling were increased at 90 min during, and after, exercise. Phosphorylation of adipose tissue HSL paralleled changes in skeletal muscle in vivo, except HSL Ser(660) was elevated 80% in adipose compared with 35% in skeletal muscle during exercise. Studies in L6 myotubes and 3T3-L1 adipocytes revealed important tissue differences in the regulation of HSL. AMPK inhibited epinephrine-induced HSL activity in L6 myotubes and was associated with reduced HSL Ser(660) but not Ser(563) phosphorylation. HSL activity was reduced in L6 myotubes expressing constitutively active AMPK, confirming the inhibitory effects of AMPK on HSL activity. Conversely, in 3T3-L1 adipocytes, AMPK activation after epinephrine stimulation did not prevent HSL activity or glycerol release, which coincided with maintenance of HSL Ser(660) phosphorylation. Taken together, these data indicate that HSL activity is maintained in the face of AMPK activation as a result of elevated HSL Ser(660) phosphorylation in adipose tissue but not skeletal muscle.

eng

IM

MEDLINE

0193-1849

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NLM

E500-8

pubmed-meshheading:16188906-3T3-L1 Cells, pubmed-meshheading:16188906-AMP-Activated Protein Kinases, pubmed-meshheading:16188906-Adipose Tissue, pubmed-meshheading:16188906-Adrenergic Agonists, pubmed-meshheading:16188906-Adult, pubmed-meshheading:16188906-Aminoimidazole Carboxamide, pubmed-meshheading:16188906-Animals, pubmed-meshheading:16188906-Biopsy, Fine-Needle, pubmed-meshheading:16188906-Enzyme Activators, pubmed-meshheading:16188906-Epinephrine, pubmed-meshheading:16188906-Exercise, pubmed-meshheading:16188906-Female, pubmed-meshheading:16188906-Humans, pubmed-meshheading:16188906-Male, pubmed-meshheading:16188906-Mice, pubmed-meshheading:16188906-Multienzyme Complexes, pubmed-meshheading:16188906-Muscle, Skeletal, pubmed-meshheading:16188906-Phosphorylation, pubmed-meshheading:16188906-Protein-Serine-Threonine Kinases, pubmed-meshheading:16188906-Ribonucleotides, pubmed-meshheading:16188906-Serine, pubmed-meshheading:16188906-Sterol Esterase, pubmed-meshheading:16188906-Triglycerides

Regulation of HSL serine phosphorylation in skeletal muscle and adipose tissue.

Journal Article, Research Support, Non-U.S. Gov't