Peroxisome proliferator-activated receptors, PPARs, (NR1C) are nuclear horm
one receptors implicated in energy homeostasis. Upon activation, these liga
nd-inducible transcription factors stimulate gene expression by binding to
the promoter of target genes. The different structural domains of PPARs are
presented in terms of activation mechanisms, namely ligand binding, phosph
orylation, and cofactor interaction. The specificity of ligands, such as fa
tty acids, eicosanoids, fibrates and thiazolidinediones (TZD), is described
for each of the three PPAR isotypes, alpha (NR1C1), beta (NR1C2) and gamma
(NR1C3), so as the differential tissue distribution of these isotypes. Fin
ally, general and specific functions of the PPAR isotypes are discussed, na
mely their implication in the control of inflammatory responses, cell proli
feration and differentiation, the roles of PPAR alpha in fatty acid catabol
ism and of PPAR gamma in adipogenesis. (C) 2000 Elsevier Science B.V. All r
ights reserved.