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人唾液的自上而下蛋白质组学分析揭示了肥大细胞病患者蛋白质谱的显著变化。

Top-Down Proteomics of Human Saliva Discloses Significant Variations of the Protein Profile in Patients with Mastocytosis.

机构信息

Dipartimento di Scienze della Vita e dell'Ambiente, Università di Cagliari, 09124 Cagliari, Italy.

Dipartimento di Scienze Mediche e Sanità Pubblica, Università di Cagliari, 09124 Cagliari, Italy.

出版信息

J Proteome Res. 2020 Aug 7;19(8):3238-3253. doi: 10.1021/acs.jproteome.0c00207. Epub 2020 Jul 6.

Abstract

Mastocytosis is a myeloproliferative neoplasm causing abnormal clonal mast cell accumulation in different tissues, such as skin and bone marrow. A cutaneous subtype (CM) is distinguished from a systemic one (SM); SM patients can be grouped into SM with (SM+C) or without (SM-C) additional cutaneous lesions, and their classification is often challenging. This study was purposed to highlight variations in the salivary proteome of patients with different mastocytosis subtypes and compared to healthy controls. A top-down proteomics approach coupled to a label-free quantitation revealed salivary profiles in patients different from those of controls and a down-regulation of peptides/proteins involved in the mouth homeostasis and defense, such as statherin, histatins, and acidic proline-rich proteins (aPRPs), and in innate immunity and inflammation, such as the cathepsin inhibitors, suggesting a systemic condition associated with an exacerbated inflammatory state. The up-regulation of antileukoproteinase and S100A8 suggested a protective role against the disease status. The two SM forms were distinguished by the lower levels of truncated forms of aPRPs, statherin, P-B peptide, and cystatin D and the higher levels of thymosin β4 and α-defensins 1 and 4 in SM-C patients with respect to SM+C. Data are available via ProteomeXchange with identifier PXD017759.

摘要

肥大细胞增多症是一种骨髓增生性肿瘤,导致异常克隆肥大细胞在不同组织(如皮肤和骨髓)中积聚。有一种皮肤亚型(CM)与系统性肥大细胞增多症(SM)不同;SM 患者可分为伴有(SM+C)或不伴有(SM-C)皮肤病变的 SM,其分类通常具有挑战性。本研究旨在强调不同肥大细胞增多症亚型患者唾液蛋白质组的变化,并与健康对照组进行比较。一种自上而下的蛋白质组学方法结合无标记定量揭示了患者唾液谱与对照组不同,并且与口腔内稳态和防御相关的肽/蛋白质(如 statherin、histatins 和酸性富含脯氨酸蛋白(aPRPs))以及固有免疫和炎症(如组织蛋白酶抑制剂)下调,表明与炎症状态加剧相关的全身性疾病。抗白细胞蛋白酶和 S100A8 的上调表明其具有针对疾病状态的保护作用。与 SM+C 相比,SM-C 患者的 aPRPs、statherin、P-B 肽和胱抑素 D 的截断形式水平较低,胸腺素β4 和α-防御素 1 和 4 的水平较高,这两种 SM 形式得以区分。数据可通过 ProteomeXchange 以标识符 PXD017759 获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7299/8008451/284f3661eac4/pr0c00207_0001.jpg

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