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Interactions of genes in intersecting signaling pathways, as well as environmental influences, are required for the development of psoriasis. Peroxisome proliferator-activated receptor gamma ( PPARγ ) is a nuclear receptor and transcription factor which inhibits the expression of many proinflammatory genes. We tested the hypothesis that low levels of  PPARγ  expression promote the development of psoriatic lesions. We combined experimental results and network functional analysis to reconstruct the model of  PPARγ -downregulated signaling in psoriasis. We hypothesize that the expression of  IL17 ,  STAT3 ,  FOXP3 , and  RORC  and  FOSL1  genes in psoriatic skin is correlated with the level of  PPARγ  expression, and they belong to the same signaling pathway that regulates the development of psoriasis lesion.

The Model of PPARγ-Downregulated Signaling in Psoriasis