Department of Environmental Toxicology and Forensic Science Graduate Program, University of California Davis, Davis, California, United States of America.
PLoS One. 2013 Oct 9;8(10):e75355. doi: 10.1371/journal.pone.0075355. eCollection 2013.
To explore the usefulness of protein profiling for characterization of ichthyoses, we here determined the profile of human epidermal stratum corneum by shotgun proteomics. Samples were analyzed after collection on tape circles from six anatomic sites (forearm, palm, lower leg, forehead, abdomen, upper back), demonstrating site-specific differences in profiles. Additional samples were collected from the forearms of subjects with ichthyosis vulgaris (filaggrin (FLG) deficiency), recessive X-linked ichthyosis (steroid sulfatase (STS) deficiency) and autosomal recessive congenital ichthyosis type lamellar ichthyosis (transglutaminase 1 (TGM1) deficiency). The ichthyosis protein expression patterns were readily distinguishable from each other and from phenotypically normal epidermis. In general, the degree of departure from normal was lower from ichthyosis vulgaris than from lamellar ichthyosis, parallel to the severity of the phenotype. Analysis of samples from families with ichthyosis vulgaris and concomitant modifying gene mutations (STS deficiency, GJB2 deficiency) permitted correlation of alterations in protein profile with more complex genetic constellations.
为了探索蛋白质谱分析在鱼鳞病特征描述中的作用,我们采用蛋白质组学的鸟枪法对人表皮角质层进行了分析。在从六个解剖部位(前臂、手掌、小腿、额头、腹部、上背部)的胶带环上收集样本后,对样本进行了分析,结果显示图谱存在部位特异性差异。另外,我们还从寻常型鱼鳞病(角蛋白丝聚合蛋白(FLG)缺陷)、隐性 X 连锁鱼鳞病(类固醇硫酸酯酶(STS)缺陷)和常染色体隐性先天性鱼鳞病样红皮病(转谷氨酰胺酶 1(TGM1)缺陷)患者的前臂上收集了样本。鱼鳞病的蛋白表达模式彼此之间以及与表型正常的表皮之间都很容易区分。一般来说,与层状鱼鳞病相比,寻常型鱼鳞病与正常表型的偏离程度较低,这与表型的严重程度相符。对伴有鱼鳞病修饰基因突变(STS 缺陷、GJB2 缺陷)的家族样本进行分析,使我们能够将蛋白图谱的改变与更为复杂的遗传结构相关联。