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GRP78 促进牙周膜干细胞的成骨和血管生成反应。

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

机构信息

Department of Oral Biology, University of Illinois at Chicago, Chicago, Illinois 60612,

出版信息

Eur Cell Mater. 2023 Jan 23;45:14-30. doi: 10.22203/eCM.v045a02.


DOI:10.22203/eCM.v045a02
PMID:36683528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10243372/
Abstract

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.

摘要

牙周炎是一种进行性疾病,最终会导致骨和牙齿丧失。牙周病的一个主要后果是无法在牙周组织中重新获得丢失的骨。葡萄糖调节蛋白-78(GRP78)在牙周韧带干细胞的成骨分化及其在牙周组织再生中的潜在用途方面的重要性已经得到了证明。先前的研究表明,GRP78 与牙本质基质蛋白-1(DMP1)之间存在关系。在这项研究中,证实了该受体-配体复合物在支持成骨和血管生成过程中的重要性。为了证明 GRP78 在矿化组织中的功能,生成了过表达或沉默 GRP78 的转基因牙周韧带干细胞(PDLSCs)。在成骨条件下培养的细胞的基因表达分析显示,GRP78 过表达时关键成骨基因的表达增加。还进行了 RNA-Seq 分析,以了解与基因型变化相关的转录组谱。使用数据库进行注释、可视化和综合发现(DAVID)对差异表达基因进行功能富集分析,证明了 GRP78 过表达时促进成骨和血管生成的基因上调。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伴随着钙沉积增加。使用皮下植入啮齿动物模型显示了 GRP78 在体内的成骨和血管生成功能。结果表明,PDLSCs 中的 GRP78 可以调节成骨和血管生成的表达。因此,GRP78 可以被认为是治疗疾病性牙周组织的靶点。

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本文引用的文献

[1]
PTX3 Effects on Osteogenic Differentiation in Osteoporosis: An In Vitro Study.

Int J Mol Sci. 2021-5-31

[2]
STIM1 a calcium sensor promotes the assembly of an ECM that contains Extracellular vesicles and factors that modulate mineralization.

Acta Biomater. 2021-1-15

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Stem Cells Int. 2020-7-8

[4]
Endocytic Trafficking of DMP1 and GRP78 Complex Facilitates Osteogenic Differentiation of Human Periodontal Ligament Stem Cells.

Front Physiol. 2019-9-12

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Front Physiol. 2018-8-15

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J Periodontol. 2018-6

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Two Transcripts of FBXO5 Promote Migration and Osteogenic Differentiation of Human Periodontal Ligament Mesenchymal Stem Cells.

Biomed Res Int. 2018-4-19

[10]
CYR61/CCN1 Regulates Sclerostin Levels and Bone Maintenance.

J Bone Miner Res. 2018-3-5

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