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一种新型分子 SLURP-1 可增强牙周韧带成纤维细胞的存活率。

A novel molecule, SLURP-1, enhances the survival of periodontal ligament fibroblasts.

机构信息

School of Dentistry, Oral Biology Research Laboratory, Faculty of Medicine, Dentistry and Health Sciences, University of Western Australia, Nedlands, WA, Australia.

出版信息

J Periodontal Res. 2010 Jun;45(3):331-6. doi: 10.1111/j.1600-0765.2009.01240.x. Epub 2010 Mar 9.

Abstract

BACKGROUND AND OBJECTIVE

The mechanism behind the survival of periodontal ligament fibroblasts is critical for the maintenance of periodontal ligament tissue. However, the number of known proteins that are involved in this action is limited. The aim of this study was to examine the role of a novel molecule, secreted mammalian Ly-6/urokinase-type plasminogen activator receptor-related protein 1 (SLURP-1), in periodontal ligament fibroblast survival.

MATERIAL AND METHODS

Human periodontal ligament fibroblasts were isolated from eight healthy human donors using established protocols. Gene expression for SLURP-1 was analysed using the reverse transcriptase-polymerase chain reaction, while protein expression was examined by immunoblotting with a SLURP-1 antibody. In addition, the apoptotic effect was examined using the terminal deoxynucleotidyl transferase-mediated dUTP nick end labelling assay.

RESULTS

Messenger RNA for SLURP-1 was expressed in the periodontal ligament, gingival fibroblasts, oral keratinocytes and bone. Moreover, the protein was secreted by both periodontal ligament and gingival fibroblasts. Functional analysis revealed that SLURP-1 substantially enhanced cell survival in periodontal ligament fibroblasts by the anti-apoptotic signal phosphatidylinositol 3-kinase.

CONCLUSION

These findings suggest that SLURP-1 may play an important role in the control and maintenance of the periodontal ligament by protecting the periodontal ligament fibroblasts from apoptosis.

摘要

背景与目的

牙周膜成纤维细胞存活的机制对于维持牙周膜组织至关重要。然而,目前已知参与这一作用的蛋白数量有限。本研究旨在探讨一种新型分子——分泌型哺乳动物 Ly-6/尿激酶型纤溶酶原激活物受体相关蛋白 1(SLURP-1)在牙周膜成纤维细胞存活中的作用。

材料与方法

采用已建立的方案,从 8 名健康供体中分离出人牙周膜成纤维细胞。采用逆转录-聚合酶链反应分析 SLURP-1 的基因表达,并用 SLURP-1 抗体进行免疫印迹检测蛋白质表达。此外,还通过末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记法检测细胞凋亡效应。

结果

SLURP-1 的信使 RNA 在牙周膜、牙龈成纤维细胞、口腔角质形成细胞和骨中表达。此外,牙周膜和成纤维牙龈细胞均可分泌 SLURP-1 蛋白。功能分析表明,SLURP-1 通过抗凋亡信号磷脂酰肌醇 3-激酶显著增强牙周膜成纤维细胞的存活。

结论

这些发现表明,SLURP-1 可能通过保护牙周膜成纤维细胞免于凋亡,在控制和维持牙周膜中发挥重要作用。

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