Suppr超能文献

骨髓间充质干细胞通过缝隙连接向脊髓损伤大鼠运动神经元的线粒体转移。

Mitochondrial Transfer from Bone Marrow Mesenchymal Stem Cells to Motor Neurons in Spinal Cord Injury Rats via Gap Junction.

机构信息

Department of Basic Medicine Sciences, Zhejiang University School of Medicine, Hangzhou 310058, China.

Department of Orthopedic Surgery, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou 310009, China.

出版信息

Theranostics. 2019 Mar 17;9(7):2017-2035. doi: 10.7150/thno.29400. eCollection 2019.

Abstract

Recent studies have demonstrated that bone marrow mesenchymal stem cells (BMSCs) protect the injured neurons of spinal cord injury (SCI) from apoptosis while the underlying mechanism of the protective effect of BMSCs remains unclear. In this study, we found the transfer of mitochondria from BMSCs to injured motor neurons and detected the functional improvement after transplanting. Primary rat BMSCs were co-cultured with oxygen-glucose deprivation (OGD) injured VSC4.1 motor neurons or primary cortical neurons. FACS analysis was used to detect the transfer of mitochondria from BMSCs to neurons. The bioenergetics profiling of neurons was detected by Extracellular Flux Analysis. Cell viability and apoptosis were also measured. BMSCs and isolated mitochondria were transplanted into SCI rats. TdT-mediated dUTP nick end labelling staining was used to detect apoptotic neurons in the ventral horn. Immunohistochemistry and Western blotting were used to measure protein expression. Re-myelination was examined by transmission electron microscope. BBB scores were used to assess locomotor function. MitoTracker-Red labelled mitochondria of BMSCs could be transferred to the OGD injured neurons. The gap junction intercellular communication (GJIC) potentiator retinoid acid increased the quantity of mitochondria transfer from BMSCs to neurons, while GJIC inhibitor 18β glycyrrhetinic acid decreased mitochondria transfer. Internalization of mitochondria improved the bioenergetics profile, decreased apoptosis and promoted cell survival in post-OGD motor neurons. Furthermore, both transplantation of mitochondria and BMSCs to the injured spinal cord improved locomotor functional recovery in SCI rats. To our knowledge, this is the first evidence that BMSCs protect against SCI through GJIC to transfer mitochondrial to the injured neurons. Our findings suggested a new therapy strategy of mitochondria transfer for the patients with SCI.

摘要

最近的研究表明,骨髓间充质干细胞(BMSCs)可以保护脊髓损伤(SCI)中受损的神经元免于凋亡,但其保护作用的潜在机制尚不清楚。在本研究中,我们发现 BMSCs 将线粒体从供体细胞转移到受损的运动神经元中,并检测到移植后的功能改善。 原代大鼠 BMSCs 与氧葡萄糖剥夺(OGD)损伤的 VSC4.1 运动神经元或原代皮质神经元共培养。使用流式细胞术分析检测 BMSCs 向神经元转移线粒体的情况。通过细胞外通量分析检测神经元的生物能谱。还测量了细胞活力和细胞凋亡。将 BMSCs 和分离的线粒体移植到 SCI 大鼠中。TdT 介导的 dUTP 缺口末端标记染色用于检测腹角中凋亡的神经元。免疫组织化学和 Western blot 用于测量蛋白质表达。通过透射电子显微镜检查髓鞘再形成。BBB 评分用于评估运动功能。 MitoTracker-Red 标记的 BMSCs 线粒体可转移至 OGD 损伤的神经元。间隙连接细胞间通讯(GJIC)增强剂视黄酸增加了 BMSCs 向神经元转移的线粒体数量,而 GJIC 抑制剂 18β 甘草次酸减少了线粒体的转移。线粒体内化改善了 OGD 运动神经元的生物能谱,减少了细胞凋亡并促进了细胞存活。此外,将线粒体和 BMSCs 移植到受伤的脊髓中均可改善 SCI 大鼠的运动功能恢复。 据我们所知,这是第一个证明 BMSCs 通过 GJIC 保护 SCI 的证据,即将线粒体转移到受损的神经元中。我们的研究结果为 SCI 患者提供了一种新的线粒体转移治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/059f/6485285/fa64b9d76ea6/thnov09p2017g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验