Protein kinase C mediates tumor necrosis factor-alpha-induced inhibition of obese gene expression and leptin secretion in brown adipocytes

Naunyn Schmiedebergs Arch Pharmacol. 1999 Dec;360(6):691-8. doi: 10.1007/s002109900134.

Abstract

Previously we showed that tumor necrosis factor-alpha (TNF-alpha) inhibits lipoprotein lipase (LPL) activity and its gene expression, an early marker of adipocyte differentiation, in cultured brown adipocytes. To know whether TNF-alpha also affects late events in brown adipocyte maturation, we examined the effect of TNF-alpha on obese gene expression and leptin secretion in mouse brown adipocytes differentiated in culture. TNF-alpha caused a concentration-dependent decrease in leptin accumulation in culture medium and leptin mRNA amount in brown adipocytes which constitutively express the ob gene. Time-course study showed that TNF-alpha significantly suppressed leptin secretion during incubation for 16, 24 and 48 h. Since some effect of TNF-alpha is mediated by activation of protein kinase C (PKC), the role of PKC in TNF-alpha-induced downregulation of ob gene expression and leptin secretion was studied. The suppressive effect of TNF-alpha on both ob gene expression and leptin secretion was blocked by PKC inhibitors such as bisindolylmaleimide I (BIM) and 1-(5-isoquinolinesulfonyl)-2-methylpiperazine dihydrochloride (H-7). Incubation of brown adipocytes with TNF-alpha (20 ng/ml, 15 min) caused a rapid shift of PKC activity from the cytosolic to the membrane fraction, suggesting an activation of PKC by TNF-alpha in brown adipocytes. This effect of TNF-alpha was blocked by a selective PKC inhibitor, BIM. These results suggest that TNF-alpha promotes dedifferentiation of the brown adipocytes as evidenced by a downregulation in ob gene expression and leptin secretion via PKC-dependent mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine / pharmacology
  • Adipocytes / cytology
  • Adipocytes / enzymology
  • Adipose Tissue, Brown / cytology
  • Adipose Tissue, Brown / enzymology*
  • Animals
  • Cell Differentiation / drug effects
  • Cell Membrane / drug effects
  • Cell Membrane / enzymology
  • Cells, Cultured
  • Cytosol / drug effects
  • Cytosol / enzymology
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Enzyme Inhibitors / pharmacology
  • Gene Expression Regulation / drug effects
  • Glycerolphosphate Dehydrogenase / metabolism
  • Indoles / pharmacology
  • Leptin / genetics*
  • Leptin / metabolism*
  • Male
  • Maleimides / pharmacology
  • Mice
  • Mice, Inbred ICR
  • Protein Kinase C / metabolism*
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / metabolism*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Enzyme Inhibitors
  • Indoles
  • Leptin
  • Maleimides
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • Glycerolphosphate Dehydrogenase
  • Protein Kinase C
  • bisindolylmaleimide I