Rittié Laure, Tejasvi Trilokraj, Harms Paul W, Xing Xianying, Nair Rajan P, Gudjonsson Johann E, Swindell William R, Elder James T
Department of Dermatology, University of Michigan, Ann Arbor, Michigan, USA.
Department of Dermatology, University of Michigan, Ann Arbor, Michigan, USA; Ann Arbor Veterans Affairs Hospital, Ann Arbor, Michigan, USA.
J Invest Dermatol. 2016 Sep;136(9):1792-1800. doi: 10.1016/j.jid.2016.05.113. Epub 2016 Jun 14.
In a transcriptome study of lesional psoriatic skin (PP) versus normal skin, we found a coexpressed gene module (N5) enriched 11.5-fold for lipid biosynthetic genes. We also observed fewer visible hairs in PP skin, compared with uninvolved nonlesional psoriatic skin or normal skin (P < 0.0001). To ask whether these findings might be due to abnormalities of the pilosebaceous unit, we carried out three-dimensional morphometric analysis of paired PP and nonlesional psoriatic skin biopsies. Sebaceous glands were markedly atrophic in PP versus nonlesional psoriatic skin (91% average reduction in volume, P = 0.031). Module N5 genes were strongly downregulated in PP versus normal skin (fold change < 0.25, 44.4-fold) and strongly upregulated in sebaceous hyperplasia (fold change > 4, 54.1-fold). The intersection of PP-downregulated and sebaceous hyperplasia-upregulated gene lists generated a gene expression signature consisting solely of module N5 genes, whose expression in PP versus normal skin was inversely correlated with the signature of IL17-stimulated keratinocytes. Despite loss of visible hairs, morphometry identified elongated follicles in PP versus nonlesional psoriatic skin (average 1.7 vs. 1.2 μm, P = 0.020). These results document sebaceous gland atrophy in nonscalp psoriasis, identify a cytokine-regulated set of sebaceous gland signature genes, and suggest that loss of visible hair in PP skin may result from abnormal sebaceous gland function.
在一项针对银屑病皮损(PP)与正常皮肤的转录组研究中,我们发现一个共表达基因模块(N5),其中脂质生物合成基因富集了11.5倍。我们还观察到,与未受累的非银屑病皮损皮肤或正常皮肤相比,PP皮肤中的可见毛发较少(P < 0.0001)。为了探究这些发现是否可能归因于皮脂腺单位的异常,我们对配对的PP和非银屑病皮损皮肤活检样本进行了三维形态计量分析。与非银屑病皮损皮肤相比,PP中的皮脂腺明显萎缩(体积平均减少91%,P = 0.031)。与正常皮肤相比,模块N5基因在PP中强烈下调(变化倍数<0.25,44.4倍),在皮脂腺增生中强烈上调(变化倍数>4,54.1倍)。PP下调基因列表与皮脂腺增生上调基因列表的交集产生了一个仅由模块N5基因组成的基因表达特征,其在PP与正常皮肤中的表达与IL17刺激的角质形成细胞的特征呈负相关。尽管可见毛发减少,但形态计量学发现PP中的毛囊相对于非银屑病皮损皮肤拉长(平均1.7对1.2μm,P = 0.020)。这些结果证明了非头皮银屑病中皮脂腺萎缩,鉴定了一组细胞因子调节的皮脂腺特征基因,并表明PP皮肤中可见毛发的减少可能是皮脂腺功能异常所致。