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

Lan Luo, Wan Hao Yan, Feng Qiu Zhang, Zhi Peng Fan
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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.

CB1 通过增强骨髓间充质干细胞的线粒体转移促进牙周韧带干细胞的成骨分化潜能
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韧带干细胞(PDLSCs)成骨分化的作用和机制:方法:在骨间充质干细胞(BMSCs)和牙周韧带干细胞(PDLSCs)中进行线粒体双向转移。采用激光共聚焦显微镜和定量流式细胞术观察线粒体转移和线粒体定量转移效率。采用实时反转录聚合酶链反应(RT-PCR)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:在 BMSCs 和 PDLSCs 之间观察到线粒体的双向转移。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 的条件培养基能显著增强 PDLSCs 的矿化能力。去除 HA-CB1 BMSCs 条件培养基中的线粒体后,PDLSCs 的矿化能力并没有增强。HO-1、PGC-1α、NRF-1、ND1和HK2在HA-CB1 BMSCs中的表达水平明显提高:结论:HA-CB1 BMSCs的CM能明显增强炎症微环境中PDLSCs受损的成骨分化能力,CM中的线粒体发挥了重要作用。CB1与HO-1/PGC-1α/NRF-1线粒体生物生成途径的激活有关,并能显著提高BMSCs中线粒体的含量。
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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