GRP78 可促进牙周韧带干细胞的成骨和血管生成反应。

IF 3.2 3区 医学 Q3 CELL & TISSUE ENGINEERING European cells & materials Pub Date : 2023-01-23 DOI:10.22203/eCM.v045a02
A Merkel, Y Chen, C Villani, A George
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引用次数: 0

摘要

牙周炎是一种渐进性疾病,最终会导致牙槽骨和牙齿脱落。牙周病的一个主要后果是无法恢复牙周丧失的骨质。葡萄糖调节蛋白-78(GRP78)在牙周韧带干细胞成骨分化中的重要性及其用于牙周再生的潜力已得到证实。之前的研究显示了 GRP78 与牙本质基质蛋白-1(DMP1)之间的关系。本研究证实了这种受体配体复合物在支持成骨和血管生成过程中的重要性。为了显示 GRP78 在矿化组织中的功能,研究人员产生了转基因牙周韧带干细胞(PDLSCs),在这些细胞中,GRP78 要么被过表达,要么被沉默。对在成骨条件下培养的细胞进行的基因表达分析表明,随着 GRP78 的过表达,关键的成骨基因有所增加。为了了解与基因型变化相关的转录组概况,还进行了 RNA-Seq 分析。利用注释、可视化和整合发现数据库(DAVID)对差异表达基因进行了功能富集分析,结果表明过表达 GRP78 会上调促进成骨和血管生成的基因。茜素红染色和扫描电子显微镜分析显示,GRP78过表达细胞的基质矿化和钙沉积增加。利用啮齿动物皮下植入模型显示了 GRP78 的体内成骨和血管生成功能。结果表明,PDLSCs 中的 GRP78 可调控成骨和血管生成的表达。因此,GRP78 可被视为修复病变牙周的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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GRP78 promotes the osteogenic and angiogenic response in periodontal ligament stem cells.

Periodontitis is a progressive disease that ultimately leads to bone and tooth loss. A major consequence of periodontal disease is the inability to regain lost bone in the periodontium. The importance was demonstrated of glucose-regulated protein-78 (GRP78) in the osteogenic differentiation of periodontal ligament stem cells and their potential use for regeneration of the periodontium. Previous studies have shown the relationship between GRP78 and dentine matrix protein-1 (DMP1). The importance of this receptor-ligand complex in supporting the process of osteogenesis and angiogenesis was confirmed in this study. To show the function of GRP78 in mineralised tissues, transgenic periodontal ligament stem cells (PDLSCs) were generated in which GRP78 was either overexpressed or silenced. Gene expression analysis of the cells cultured under osteogenic conditions showed an increase in key osteogenic genes with the overexpression of GRP78. RNA-Seq analysis was also performed to understand the transcriptome profile associated with genotype changes. Using the database for annotation, visualisation, and integration discovery (DAVID) for the functional enrichment analysis of differentially expressed genes, the upregulation of genes promoting osteogenesis and angiogenesis with GRP78 overexpression was demonstrated. Alizarin red staining and scanning electron microscopy analysis revealed matrix mineralisation with increased calcium deposition in GRP78 overexpressing cells. The in vivo osteogenic and angiogenic function of GRP78 was shown using a subcutaneous implantation rodent model. The results suggested that GRP78 in PDLSCs can regulate the expression of both osteogenesis and angiogenesis. Therefore, GRP78 could be considered as a therapeutic target for repair of diseased periodontium.

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来源期刊
European cells & materials
European cells & materials 生物-材料科学:生物材料
CiteScore
6.00
自引率
6.50%
发文量
55
审稿时长
1.5 months
期刊介绍: eCM provides an interdisciplinary forum for publication of preclinical research in the musculoskeletal field (Trauma, Maxillofacial (including dental), Spine and Orthopaedics). The clinical relevance of the work must be briefly mentioned within the abstract, and in more detail in the paper. Poor abstracts which do not concisely cover the paper contents will not be sent for review. Incremental steps in research will not be entertained by eCM journal.Cross-disciplinary papers that go across our scope areas are welcomed.
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