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PMID: 10623894 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Stimulation of adipose differentiation related protein (ADRP) expression in adipocyte precursors by long-chain fatty acids.

Journal of cellular physiology ·Vol. 182 ·No. 2 ·2000-02-00 ·Pages 297-302

Gao J, Ye H, Serrero G

Abstract

Adipose differentiation related protein (ADRP) is a 50-kDa protein expressed in adipocytes and transcriptionally activated when adipocyte precursors differentiate into mature adipocytes. Recent experiments have demonstrated that ADRP is a fatty acid binding protein that specifically facilitates the uptake of long-chain fatty acids. The present investigation provides evidence that ADRP mRNA and protein expression in preadipocytes is stimulated by fatty acids in a time- and dose-dependent fashion. ADRP mRNA expression was maximally stimulated at fatty acid concentrations of or above 10(-5) M. Stimulation of ADRP expression was observed with the nonmetabolizable fatty acid 2-bromopalmitate and with natural fatty acids. Stimulation of ADRP mRNA expression by fatty acids peaked between 5 and 8 hr and decreased by 24 hr. Stimulation of ADRP expression by fatty acids was completely inhibited by treatment with actinomycin D, suggesting that fatty acid stimulates ADRP gene expression at the transcriptional level. Comparison of the effect of several fatty acids with varying carbon chain lengths indicated that long-chain fatty acids were active in stimulating ADRP, whereas short-chain fatty acids such as caproate and 2-bromooctanoate had no effect. The degree of saturation of fatty acids did not influence their ability to stimulate ADRP expression. These studies provide new information on the regulation of ADRP and identify a new target regulated by fatty acids during adipose differentiation.

MeSH Terms
Adipocytes/drug effects,metabolism Animals Dose-Response Relationship, Drug Membrane Proteins/genetics,metabolism Mice Oleic Acid/chemistry,pharmacology Palmitates/chemistry,pharmacology Perilipin-2 RNA, Messenger/metabolism Stem Cells/drug effects,metabolism Time Factors Transcription, Genetic/drug effects Tumor Cells, Cultured
Chemicals
Membrane Proteins Palmitates Perilipin-2 Plin2 protein, mouse RNA, Messenger 2-bromopalmitate Oleic Acid
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Gao J
Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy and Program of Oncology, Marlene and Stewart Greenebaum Cancer Center, Baltimore, MD 21201-1180, USA.
Ye H
Serrero G
Article Info
Journal
Journal of cellular physiology
Abbr.
J Cell Physiol
ISSN
0021-9541
Published
2000-02-00
Pages
297-302
Language
English
Region
United States
NLM ID
0050222
Subset
IM
Grants
NIDDK NIH HHS · R01 DK 51463 · United States
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