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
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.