ADRP/adipophilin is degraded through the proteasome-dependent pathway during regression of lipid-storing cells

Yutaka Masuda, Hiroyuki Itabe, Miho Odaki, Kotaro Hama, Yasuyuki Fujimoto, Masahiro Mori, Naoko Sasabe, Junken Aoki, Hiroyuki Arai, Tatsuya Takano

Research output: Contribution to journalArticlepeer-review

106 Citations (Scopus)


Adipose differentiation-related protein (ADRP) is a major protein associated with lipid droplets in various types of cells, including macrophage-derived foam cells and liver cells. However, the role of ADRP in the processes of formation and regression of these cells is not understood. When J774 murine macrophages were incubated with either VLDL or oleic acid, their content of both ADRP and triacylglycerol (TG) increased 3- to 4-fold. Induction of ADRP during TG accumulation was also observed in oleic acid-treated HuH-7 human liver cells. Addition of triacsin C, a potent inhibitor of acyl-CoA synthase, for 6 h decreased the amount of TG in VLDL-induced foam cells and oleic acid-treated liver cells; it decreased the amount of ADRP protein in parallel, indicating the amount of ADRP reduced during regression of the lipid-storing cells. Addition of a proteasome inhibitor during triacsin C treatment abolished the ADRP decrease and accumulated polyubiquitinated ADRP. In addition, the proteasome inhibitor reversed not only the degradation of ADRP but also TG reduction by triacsin C. These results suggest that cellular amounts of ADRP and TG regulate each other and that the ubiquitin-proteasome system is involved in degradation of ADRP during regression of lipid-storing cells.

Original languageEnglish
Pages (from-to)87-98
Number of pages12
JournalJournal of lipid research
Issue number1
Publication statusPublished - 2006 Jan
Externally publishedYes


  • Adipose differentiation-related protein
  • Lipid droplets
  • Liver cells
  • Macrophages
  • Triacylglycerol
  • VLDL

ASJC Scopus subject areas

  • Biochemistry
  • Endocrinology
  • Cell Biology


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