首页|骨髓间充质干细胞来源的外泌体抑制地塞米松诱导的C2C12肌管萎缩

骨髓间充质干细胞来源的外泌体抑制地塞米松诱导的C2C12肌管萎缩

扫码查看
目的 研究骨髓间充质干细胞(bone marrow mesenchy-mal stem cells,BMSCs)来源的外泌体(exsomes,EXOs)对地塞米松(dexamethasone,DEX)诱导的C2C12肌管萎缩的影响。方法 (1)分离提取培养C57BL/6J小鼠BMSCs。(2)提取并鉴定BMSCs-EXOs。(3)C2C12细胞成肌分化。(4)将肌管细胞分为对照组(Control,2%马血清培养基培养48 h)、地塞米松组(DEX、浓度为10 μmol·L-1的DEX干预肌管48 h)、外泌体组(EXOs、外泌体干预肌管48 h)、外泌体抑制剂组(GW4869、10 μmol的GW4869干预BMSCs后提取的外泌体干预肌管48 h)。48 h后测量各组肌管直径,CCK-8法检测各组细胞活力,Western blot检测各组肌肉萎缩及成肌分化相关蛋白的表达量。结果 BMSCs呈长梭形,BM-SCs-EXOs在透射电镜下为圆形的双层膜结构,直径约200 nm,且高表达CD9、CD63和CD81。相比于Control组,DEX组细胞活性降低(P<0。01),肌管细胞直径减少(P<0。01),atrogin-1(P<0。05)和 MuRF-1(P<0。01)的表达明显上调,MYOD(P<0。01)蛋白表达降低;相比于DEX组,BMSCs-EXOs组细胞活性升高(P<0。01),肌管细胞直径增加(P<0。01),atrogin-1(P<0。05)和 MuRF-1(P<0。01)的表达明显下调,MYOD(P<0。01)蛋白表达升高;相比于BMSCs-EXOs组,BMSCs-EXOs(GW4869)组细胞活性降低(P<0。05),肌管细胞直径减少(P<0。01),atrogin-1(P<0。05)和 MuRF-1(P<0。05)的表达上调,MYOD(P<0。01)蛋白表达降低。结论 骨髓间充质干细胞来源的外泌体(BMSCs-EXOs)可抑制地塞米松诱导的C2C12肌管萎缩。
Bone marrow mesenchymal stem cell-derived exosomes inhibit dexamethasone-induced C2C12 myotube atrophy
Aim To investigate the effect of exosomes derived from bone marrod-derived mesenchymal stem cells(BMSCs)on dexamethasone-induced C2C12 muscular canal atrophy.Methods(1)C57BL/6J mouse bone marrow mesenchymal stem cells were isola-ted and cultured by whole bone marrow adhesion meth-od.(2)Extraction and identification of BMSCs EXOs were performed.(3)Myogenic differentiation of C2C12 cells was carried out.(4)The successfully differentia-ted myotubes were divided into the control group(cul-tured in 2%equine serum medium for 48 h),dexam-ethasone group(dexamethasone,DEX,10 μmol·L-1 concentration of DEX interfered with myotubes for 48 h),and exosomes group(exosomes,EXOs,interfered with myotubes for 48 h),exosome inhibitor group(exo-somes extracted from BMSCs after 10 µm GW4869 in-tervention,interfered with myotubes for 48 h).48 h later,the morphology and diameter of muscle tubes were observed and measured by microscope.Cell via-bility of each group was detected by CCK-8 method.The expression levels of atrogin-1 and MuRF-1,myo-genic differentiation antigen(MYOD)in each group were detected by Western blot.Results BMSCs were long spusiform,and BMSCS-EXOS showed a circular bilayer structure under transmission electron microsco-py,with a diameter of about 200 nm.CD9,CD63 and CD81 were highly expressed.Compared with the con-trol group,cell activity in DEX group decreased(P<0.01),diameter of myotubes decreased(P<0.01),expressions of atrogin-1(P<0.05)and MuRF-1(P<0.01)were significantly up-regulated,and expression of MYOD(P<0.01)was significantly down-regula-ted.Compared with the DEX group,cell activity in the BMSCs-EXOs group increased(P<0.01),diameter of myotubes increased(P<0.01),expressions of atrogin-1(P<0.05)and MuRF-1(P<0.01)were signifi-cantly down-regulated,and expression of MYOD(P<0.01)was up-regulated.Compared with the BMSCs-EXOs group,cell activity of the BMSCs-EXOs(GW4869)group decreased(P<0.05),diameter of myotubes decreased(P<0.01),expressions of atrog-in-1(P<0.05)and MuRF-1(P<0.05)were up-regulated,and expression of MYOD(P<0.01)was down-regulated.Conclusion Bone marrow mesen-chymal stem cell-derived exosomes(BM-MSCs-EXOs)inhibit dexamethasone-induced C2C12 muscle tube at-rophy.

bone marrow mesenchymal stem cellsdexamethasonemyotubeexosomemuscle atrophyC2C12

柯义兵、丁永宏、阿布都克热木·达吾提、郭浩然、兰志杰、王勇平

展开 >

兰州大学第一临床医学院,甘肃兰州 730000

宁夏医科大学,宁夏银川 750000

兰州大学第一医院骨科,甘肃兰州 730000

骨髓间充质干细胞 外泌体 地塞米松 肌管 肌肉萎缩 C2C12

2025

中国药理学通报
中国药理学会

中国药理学通报

北大核心
影响因子:1.54
ISSN:1001-1978
年,卷(期):2025.41(1)