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瘢痕性脱发与过氧化物酶体增殖物激活受体γ的联系。

Scarring alopecia and the PPAR-gamma connection.

作者信息

Harries Matthew J, Paus Ralf

机构信息

Department of Dermatological Sciences, University of Manchester, Manchester, UK.

出版信息

J Invest Dermatol. 2009 May;129(5):1066-70. doi: 10.1038/jid.2008.425.

Abstract

The pathobiology of primary cicatricial ("scarring") alopecia (PCA) remains poorly understood and underinvestigated. In this issue, Karnik et al. identify a previously unsuspected player, peroxisome proliferator-activated receptor-gamma (PPARgamma), in the pathogenesis of the most frequent form of PCA, lichen planopilaris (LPP). The authors show that PPARgamma is required for maintenance of a functional epithelial stem cell compartment in murine hair follicles, that the targeted deletion of PPARgamma in the bulge/isthmus area of the hair follicle epithelium generates a skin pathology that resembles LPP, and that LPP patients show gene expression changes that indicate a defect in lipid metabolism and peroxisome biogenesis. This study invites the revisitation of many open questions in PCA pathobiology and the exploration of new avenues for future PCA management.

摘要

原发性瘢痕性(“瘢痕性”)脱发(PCA)的病理生物学仍未得到充分理解和研究。在本期杂志中,卡尔尼克等人在最常见的PCA形式——扁平苔藓样毛发扁平苔藓(LPP)的发病机制中,发现了一个此前未被怀疑的因素,即过氧化物酶体增殖物激活受体γ(PPARγ)。作者表明,PPARγ是维持小鼠毛囊中功能性上皮干细胞区室所必需的,在毛囊上皮的隆突/峡部区域靶向缺失PPARγ会产生类似于LPP的皮肤病理变化,并且LPP患者表现出基因表达变化,提示脂质代谢和过氧化物酶体生物发生存在缺陷。这项研究促使人们重新审视PCA病理生物学中许多未解决的问题,并探索未来PCA治疗的新途径。

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