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[人骨髓间充质干细胞外泌体来源的miR-335-5p通过下调DKK1促进人牙周膜干细胞成骨分化以减轻牙周炎]

[Human bone marrow mesenchymal stem cell exosome-derived miR-335-5p promotes osteogenic differentiation of human periodontal ligament stem cells to alleviate periodontitis by downregulating DKK1].

作者信息

Liu Y, Zeng L, Wang W, Yang Y, Wang Z, Liu J, Li W, Sun J, Yu X

机构信息

Department of Oral and Maxillofacial Surgery, Affiliated Stomatology Hospital of Kunming Medical University, Kunming 650106, China.

Department of Stomatology, Affiliated Hospital of Yunnan University (Second People's Hospital of Yunnan Province, Yunnan Province Ophthalmology Hospital), Kunming 650021, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2023 Mar 20;43(3):420-427. doi: 10.12122/j.issn.1673-4254.2023.03.12.

DOI:10.12122/j.issn.1673-4254.2023.03.12
PMID:37087587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10122733/
Abstract

OBJECTIVE

To observe the effect of miR-335-5p derived from human bone marrow mesenchymal stem cell (hBMMSCs) exosomes on osteogenic differentiation of human periodontal ligament stem cell (PDLSCs) model of periodontitis and explore its mechanism.

METHODS

The exosomes extracted from hBMMSCs were identified by transmission electron microscopy, Western blotting and PKH67 labeling. The human PDLSC model of TNF-α-induced periodontitis were co-cultured with the extracted exosomes, and qRT-PCR was performed to detect the changes in the expressions of miR-335-5p and the mRNA levels of pro-inflammatory cytokines (IL-1β, IL-6, and IL-8) and the osteogenic marker genes (RunX2, OCN and BMP-2). Alizarin red staining and ALP staining were used to detect the formation of calcium nodules in the treated cells, and the expression level of DKK1 protein was detected with Western blotting. Dual luciferase reporter gene assay was used to verify the targeting relationship between miR-335-5p and DKK1.

RESULTS

High expressions of CD9 and CD81 were detected in the extracted hBMMSC exosomes ( < 0.05). In TNF-α-induced hPDLSCs, treatment with the extracted exosomes significantly reduced the mRNA expressions of IL-1β, IL-6 and IL-8, enhanced the mRNA expressions of RunX2, OCN, and BMP-2, and promoted the formation of calcium nodules. MiR-335-5p was highly expressed in hBMMSC-derived exosomes, and overexpression of miR-335-5p significantly downregulated DKK1 protein expression, inhibited the mRNA expressions of IL-1β, IL-6 and IL-8, and promoted the mRNA expressions of osteogenic markers and the formation of calcium nodules in hPDLSCs.

CONCLUSION

HBMMSC exosome-derived miR-335-5p promotes osteogenic differentiation of hPDLSCs and inhibits the development of periodontitis by downregulating DKK1.

摘要

目的

观察人骨髓间充质干细胞(hBMMSCs)外泌体来源的miR-335-5p对牙周炎人牙周膜干细胞(PDLSCs)模型成骨分化的影响并探讨其机制。

方法

采用透射电子显微镜、蛋白质免疫印迹法及PKH67标记对从hBMMSCs中提取的外泌体进行鉴定。将TNF-α诱导的人牙周炎PDLSC模型与提取的外泌体共培养,采用qRT-PCR检测miR-335-5p表达变化以及促炎细胞因子(IL-1β、IL-6和IL-8)和骨生成标记基因(RunX2、OCN和BMP-2)的mRNA水平。采用茜素红染色和碱性磷酸酶(ALP)染色检测处理后细胞中钙结节的形成,并用蛋白质免疫印迹法检测DKK1蛋白的表达水平。采用双荧光素酶报告基因检测法验证miR-335-5p与DKK1之间的靶向关系。

结果

在提取的hBMMSC外泌体中检测到CD9和CD81高表达(<0.05)。在TNF-α诱导的hPDLSCs中,用提取的外泌体处理可显著降低IL-1β、IL-6和IL-8的mRNA表达,增强RunX2、OCN和BMP-2的mRNA表达,并促进钙结节的形成。miR-335-5p在hBMMSC来源的外泌体中高表达,miR-335-5p过表达显著下调DKK1蛋白表达,抑制hPDLSCs中IL-1β、IL-6和IL-8的mRNA表达,并促进骨生成标记物的mRNA表达和钙结节的形成。

结论

hBMMSC外泌体来源的miR-335-5p通过下调DKK1促进hPDLSCs的成骨分化并抑制牙周炎的发展。

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