Manconi Barbara, Liori Barbara, Cabras Tiziana, Iavarone Federica, Manni Armando, Messana Irene, Castagnola Massimo, Olianas Alessandra
Dipartimento di Scienze della Vita e dell'Ambiente, Università di Cagliari, 09042, Monserrato CA, Italy.
Dipartimento di Scienze della Vita e dell'Ambiente, Università di Cagliari, 09042, Monserrato CA, Italy.
Arch Oral Biol. 2017 May;77:68-74. doi: 10.1016/j.archoralbio.2017.01.021. Epub 2017 Jan 31.
This study aims to analyze the salivary peptidome/proteome of edentulous subject with respect to dentate control subjects.
Unstimulated whole saliva, collected from 11 edentulous subjects (age 60-76 years) and 11 dentate age-matched control subjects, was immediately treated with 0.2% aqueous trifluoroacetic acid and the acidic soluble fraction analyzed by High Performace Liquid Chromatography-Mass Spectrometry. The relative abundance of the salivary peptides/proteins was determined by measuring the area of the High Performace Liquid Chromatography-Mass Spectrometry eXtracted Ion Current peaks which is linearly proportional to peptide/protein concentration under identical experimental conditions. Levels of salivary peptides/proteins in the two groups were compared by the nonparametric Mann-Whitney test to evidence statistically significant differences.
Levels of cystatin A, S-glutathionylated, S-cystenylated, S-S dimer derivatives of cystatin B and S-glutathionylated derivative of SPRR3, were found significantly higher in edentulous subjects with respect to dentate controls. The major peptides and proteins typically deriving from salivary glands did not show any statistically significant differences.
Cystatin A, S-glutathionylated, S-cystenylated, S-S dimer derivatives of cystatin B and S-glutathionylated derivative of SPRR3, which are mainly of intracellular origin and represent the major constituents of the cornified cell envelope are a clue of inflammation of mucosal epithelia.
本研究旨在分析无牙颌受试者相对于有牙对照受试者的唾液肽组/蛋白质组。
收集11名无牙颌受试者(年龄60 - 76岁)和11名年龄匹配的有牙对照受试者的非刺激性全唾液,立即用0.2%的三氟乙酸水溶液处理,并通过高效液相色谱 - 质谱法分析酸性可溶部分。通过测量高效液相色谱 - 质谱法提取离子流峰的面积来确定唾液肽/蛋白质的相对丰度,在相同实验条件下,该面积与肽/蛋白质浓度呈线性比例。通过非参数曼 - 惠特尼检验比较两组唾液肽/蛋白质的水平,以证明统计学上的显著差异。
与有牙对照相比,无牙颌受试者中胱抑素A、胱抑素B的S - 谷胱甘肽化、S - 半胱氨酸化、S - S二聚体衍生物以及SPRR3的S - 谷胱甘肽化衍生物的水平显著更高。通常源自唾液腺的主要肽和蛋白质未显示出任何统计学上的显著差异。
胱抑素A、胱抑素B的S - 谷胱甘肽化、S - 半胱氨酸化、S - S二聚体衍生物以及SPRR3的S - 谷胱甘肽化衍生物,这些主要源自细胞内且是角质化细胞包膜的主要成分,是黏膜上皮炎症的一个线索。