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CB1 通过增强骨髓间充质干细胞的线粒体转移来促进牙周膜干细胞的成骨分化潜能。

CB1 Promotes Osteogenic Differentiation Potential of Periodontal Ligament Stem Cells by Enhancing Mitochondrial Transfer of Bone Marrow Mesenchymal Stem Cells.

出版信息

Chin J Dent Res. 2024 Sep 2;27(3):225-234. doi: 10.3290/j.cjdr.b5698381.

DOI:10.3290/j.cjdr.b5698381
PMID:39221983
Abstract

OBJECTIVE

To reveal the role and mechanism of cannabinoid receptor 1 (CB1) and mitochondria in promoting osteogenic differentiation of periodontal ligament stem cells (PDLSCs) in the inflammatory microenvironment.

METHODS

Bidirectional mitochondrial transfer was performed in bone mesenchymal stem cells (BMSCs) and PDLSCs. Laser confocal microscopy and quantitative flow cytometry were used to observe the mitochondrial transfer and quantitative mitochondrial transfer efficiency. Realtime reverse transcription polymerase chain reaction (RT-PCR) was employed to detect gene expression. Alkaline phosphatase (ALP) activity, alizarin red staining (ARS) and quantitative calcium ion analysis were used to evaluate the degree of osteogenic differentiation of PDLSCs.

RESULTS

Bidirectional mitochondrial transfer was observed between BMSCs and PDLSCs. The indirect co-culture system could simulate intercellular mitochondrial transfer. Compared with the conditioned medium (CM) for BMSCs, that for HA-CB1 BMSCs could significantly enhance the mineralisation ability of PDLSCs. The mineralisation ability of PDLSCs could not be enhanced after removing the mitochondria in CM for HA-CB1 BMSCs. The expression level of HO-1, PGC-1α, NRF-1, ND1 and HK2 was significantly increased in HA-CB1 BMSCs.

CONCLUSION

CM for HA-CB1 BMSCs could significantly enhance the damaged osteogenic differentiation ability of PDLSCs in the inflammatory microenvironment, and the mitochondria of CM played an important role. CB1 was related to the activation of the HO-1/PGC-1α/NRF-1 mitochondrial biogenesis pathway, and significantly increased the mitochondrial content in BMSCs.

摘要

目的

揭示大麻素受体 1(CB1)和线粒体在炎症微环境中促进牙周膜干细胞(PDLSCs)成骨分化中的作用和机制。

方法

在骨髓间充质干细胞(BMSCs)和 PDLSCs 中进行双向线粒体转移。激光共聚焦显微镜和定量流式细胞术用于观察线粒体转移和定量线粒体转移效率。实时逆转录聚合酶链反应(RT-PCR)用于检测基因表达。碱性磷酸酶(ALP)活性、茜素红染色(ARS)和定量钙离子分析用于评估 PDLSCs 的成骨分化程度。

结果

观察到 BMSCs 和 PDLSCs 之间存在双向线粒体转移。间接共培养系统可以模拟细胞间线粒体转移。与 BMSCs 的条件培养基(CM)相比,HA-CB1 BMSCs 的 CM 可显著增强 PDLSCs 的矿化能力。去除 HA-CB1 BMSCs 的 CM 中的线粒体后,PDLSCs 的矿化能力不能增强。HA-CB1 BMSCs 中 HO-1、PGC-1α、NRF-1、ND1 和 HK2 的表达水平显著增加。

结论

HA-CB1 BMSCs 的 CM 可显著增强炎症微环境中受损的 PDLSCs 成骨分化能力,CM 中的线粒体起重要作用。CB1 与 HO-1/PGC-1α/NRF-1 线粒体生物发生途径的激活有关,可显著增加 BMSCs 中的线粒体含量。

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