Selective deletion of PPARβ/δ in fibroblasts causes dermal fibrosis by attenuated LRG1 expression

成纤维细胞中 PPARβ/δ 的选择性缺失通过减弱 LRG1 表达导致真皮纤维化

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作者:Ming Keat Sng, Jeremy Soon Kiat Chan, Ziqiang Teo, Terri Phua, Eddie Han Pin Tan, Jonathan Wei Kiat Wee, Nikki Jun Ning Koh, Chek Kun Tan, Jia Peng Chen, Mintu Pal, Benny Meng Kiat Tong, Ya Lin Tnay, Xuan Rui Ng, Pengcheng Zhu, Shunsuke Chiba, Xiaomeng Wang, Walter Wahli, Nguan Soon Tan

Abstract

Connective tissue diseases of the skin are characterized by excessive collagen deposition in the skin and internal organs. Fibroblasts play a pivotal role in the clinical presentation of these conditions. Nuclear receptor peroxisome-proliferator activated receptors (PPARs) are therapeutic targets for dermal fibrosis, but the contribution of the different PPAR subtypes are poorly understood. Particularly, the role of fibroblast PPARβ/δ in dermal fibrosis has not been elucidated. Thus, we generated a mouse strain with selective deletion of PPARβ/δ in the fibroblast (FSPCre-Pparb/d-/-) and interrogated its epidermal and dermal transcriptome profiles. We uncovered a downregulated gene, leucine-rich alpha-2-glycoprotein-1 (Lrg1), of previously unknown function in skin development and architecture. Our findings suggest that the regulation of Lrg1 by PPARβ/δ in fibroblasts is an important signaling conduit integrating PPARβ/δ and TGFβ1-signaling networks in skin health and disease. Thus, the FSPCre-Pparb/d-/- mouse model could serve as a novel tool in the current gunnery of animal models to better understand dermal fibrosis.

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