转录因子
银屑病
磷酸酶
薄荷醇
生物
细胞生物学
化学
免疫学
生物化学
基因
磷酸化
有机化学
作者
Zhikai Wang,Yang Sun,Fangzhou Lou,Jing Bai,Hong Zhou,Xiaojie Cai,Libo Sun,Qianqian Yin,Sibei Tang,Yue Wu,Fan Li,Zhenyao Xu,Hong Wang,Xiaoyu Hu,Honglin Wang
标识
DOI:10.1038/s41467-022-35565-y
摘要
Abstract Protein Phosphatase 6 down-regulation in keratinocytes is a pivotal event that amplifies the inflammatory circuits in psoriasis, indicating that restoration of protein phosphatase 6 can be a rational strategy for psoriasis treatment. Through the phenotypic screen, we here identify L-menthol that ameliorates psoriasis-like skin inflammation by increasing protein phosphatase 6 in keratinocytes. Target identification approaches reveal an indispensable role for the transcription factor hairy and enhancer of split 1 in governing the protein phosphatase 6-upregulating function of L-menthol in keratinocytes. The transcription factor hairy and enhancer of split 1 is diminished in the epidermis of psoriasis patients and imiquimod-induced mouse model, while L-menthol upregulates the transcription factor hairy and enhancer of split 1 by preventing its proteasomal degradation. Mechanistically, the transcription factor hairy and enhancer of split 1 transcriptionally activates the expression of immunoglobulin-binding protein 1 which promotes protein phosphatase 6 expression and inhibits its ubiquitination. Collectively, we discover a therapeutic compound, L-menthol, for psoriasis, and uncover the dysfunctional the transcription factor hairy and enhancer of split 1- immunoglobulin-binding protein 1- protein phosphatase 6 axis that contributes to psoriasis pathology by using L-menthol as a probe.
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