Harries Matthew J, Paus Ralf
Department of Dermatological Sciences, University of Manchester, Manchester, UK.
J Invest Dermatol. 2009 May;129(5):1066-70. doi: 10.1038/jid.2008.425.
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.
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。