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唾液的蛋白质组学分析确定了正畸牙齿移动的潜在生物标志物。

Proteomic analysis of saliva identifies potential biomarkers for orthodontic tooth movement.

作者信息

Ellias Mohd Faiz, Zainal Ariffin Shahrul Hisham, Karsani Saiful Anuar, Abdul Rahman Mariati, Senafi Shahidan, Megat Abdul Wahab Rohaya

机构信息

School of Bioscience and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Selangor, 43600 Bangi, Malaysia.

出版信息

ScientificWorldJournal. 2012;2012:647240. doi: 10.1100/2012/647240. Epub 2012 Jul 31.

Abstract

Orthodontic treatment has been shown to induce inflammation, followed by bone remodelling in the periodontium. These processes trigger the secretion of various proteins and enzymes into the saliva. This study aims to identify salivary proteins that change in expression during orthodontic tooth movement. These differentially expressed proteins can potentially serve as protein biomarkers for the monitoring of orthodontic treatment and tooth movement. Whole saliva from three healthy female subjects were collected before force application using fixed appliance and at 14 days after 0.014'' Niti wire was applied. Salivary proteins were resolved using two-dimensional gel electrophoresis (2DE) over a pH range of 3-10, and the resulting proteome profiles were compared. Differentially expressed protein spots were then identified by MALDI-TOF/TOF tandem mass spectrometry. Nine proteins were found to be differentially expressed; however, only eight were identified by MALDI-TOF/TOF. Four of these proteins-Protein S100-A9, immunoglobulin J chain, Ig alpha-1 chain C region, and CRISP-3-have known roles in inflammation and bone resorption.

摘要

正畸治疗已被证明会引发炎症,随后牙周组织会发生骨重塑。这些过程会促使各种蛋白质和酶分泌到唾液中。本研究旨在鉴定在正畸牙齿移动过程中表达发生变化的唾液蛋白质。这些差异表达的蛋白质有可能作为蛋白质生物标志物,用于监测正畸治疗和牙齿移动情况。在使用固定矫治器施加力之前以及在施加0.014英寸镍钛丝14天后,收集了三名健康女性受试者的全唾液。使用二维凝胶电泳(2DE)在pH值3 - 10的范围内分离唾液蛋白质,并比较所得的蛋白质组图谱。然后通过基质辅助激光解吸电离飞行时间串联质谱(MALDI-TOF/TOF)鉴定差异表达的蛋白质斑点。发现有9种蛋白质差异表达;然而,通过MALDI-TOF/TOF仅鉴定出8种。其中4种蛋白质——蛋白质S100-A9、免疫球蛋白J链、Igα-1链C区域和富含半胱氨酸的分泌蛋白3(CRISP-3)——在炎症和骨吸收中具有已知作用。

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