Peroxisome-proliferator-activated receptor delta mediates the effects of long-chain fatty acids on post-confluent cell proliferation

Citation
C. Jehl-pietri et al., Peroxisome-proliferator-activated receptor delta mediates the effects of long-chain fatty acids on post-confluent cell proliferation, BIOCHEM J, 350, 2000, pp. 93-98
Citations number
34
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL JOURNAL
ISSN journal
02646021 → ACNP
Volume
350
Year of publication
2000
Part
1
Pages
93 - 98
Database
ISI
SICI code
0264-6021(20000815)350:<93:PRDMTE>2.0.ZU;2-0
Abstract
Nutritional long-chain fatty acids control adipose tissue mass by regulatin g the number and the size of adipocytes. It is now established that peroxis ome-proliferator-activated receptors (PPARs) play crucial functions in the control of gene expression and the level of eel differentiation. PPAR gamma , which is activated by specific prostanoids, is a key factor in activating terminal differentiation and adipogenesis. We have recently demonstrated t hat PPAR delta, once activated by fatty acids, drives the expression of a l imited set of genes, including that encoding PPAR gamma, thereby inducing a dipose differentiation. Thus far, the mechanism of action of fatty acids in the control of preadipocyte proliferation has remained unknown. We show he re that PPAR delta is directly implicated in fatty acid-induced cell prolif eration. Ectopic expression of PPAR delta renders 3T3C2 cells capable of re sponding to INTRODUCTION treatment with long-chain fatty acids by a resumpt ion of mitosis, and this effect is limited to a few days after confluence. This response is restricted to PPAR delta activators and, for fatty acids, takes place within the range of concentrations found to trigger differentia tion of preadipocytes both in vitro and in vivo. Furthermore, the use of a mutated inactive PPAR delta demonstrated that transcriptional activity of t he nuclear receptor is required to mediate fatty acid-induced proliferation . These data demonstrate that PPAR delta, as a transcription factor, is dir ectly implicated in fatty acid-induced proliferation, and this could explai n the hyperplastic development of adipose tissue that occurs in high-fat-fe d animals.