Original Article
Subject Categories: Wound Healing
Journal of Investigative Dermatology Symposium Proceedings (2006) 11, 30–35. doi:10.1038/sj.jidsymp.5650007
Functions of the Peroxisome Proliferator-Activated Receptor (PPAR)
and
in Skin Homeostasis, Epithelial Repair, and Morphogenesis
Guillaume Icre1, Walter Wahli1 and Liliane Michalik1
1Center for Integrative Genomics, National Research Centre "Frontiers in Genetics", University of Lausanne, Le Génopode, Lausanne-Dorigny, Switzerland
Correspondence: Dr Liliane Michalik, Center for Integrative Genomics, National Research Centre "Frontiers in Genetics", University of Lausanne, Le Génopode, Lausanne CH-1015, Switzerland. E-mail: liliane.michalik@unil.ch
Received 23 December 2005; Revised 21 February 2006; Accepted 21 February 2006.
Abstract
The three peroxisome proliferator-activated receptors (PPAR
, PPAR
, and PPAR
) are ligand-activated transcription factors belonging to the nuclear hormone receptor superfamily. They are regarded as being sensors of physiological levels of fatty acids and fatty acid derivatives. In the adult mouse skin, they are found in hair follicle keratinocytes but not in interfollicular epidermis keratinocytes. Skin injury stimulates the expression of PPAR
and PPAR
at the site of the wound. Here, we review the spatiotemporal program that triggers PPAR
expression immediately after an injury, and then gradually represses it during epithelial repair. The opposing effects of the tumor necrosis factor-
and transforming growth factor-
-1 signalling pathways on the activity of the PPAR
promoter are the key elements of this regulation. We then compare the involvement of PPAR
in the skin in response to an injury and during hair morphogenesis, and underscore the similarity of its action on cell survival in both situations.
Abbreviations:
COX-2, cyclooxygenase-2; PPAR, peroxisome proliferator-activated receptor; TNF-
, tumor necrosis factor-
; TGF-
, transforming growth factor-
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