[1]宫树一 王景续 穆胜凯.微小RNA-34a对强直性脊柱炎滑膜成纤维细胞成骨分化的影响[J].中国中医骨伤科杂志,2021,29(09):1-4.
 GONG Shuyi WANG Jingxu MU Shengkai.Efficacy of miRNA-34a on the Osteogenic Differentiation ofSynovial Fibroblasts in Ankylosing Spondylitis and Its Mechanism[J].Chinese Journal of Traditional Medical Traumatology & Orthopedics,2021,29(09):1-4.
点击复制

微小RNA-34a对强直性脊柱炎滑膜成纤维细胞成骨分化的影响()
分享到:

《中国中医骨伤科杂志》[ISSN:1005-0205/CN:42-1340/R]

卷:
第29卷
期数:
2021年09期
页码:
1-4
栏目:
实验研究
出版日期:
2021-09-15

文章信息/Info

Title:
Efficacy of miRNA-34a on the Osteogenic Differentiation ofSynovial Fibroblasts in Ankylosing Spondylitis and Its Mechanism
文章编号:
1005-0205(2021)09-0001-04
作者:
宫树一1 王景续1 穆胜凯1
1沈阳市骨科医院脊柱外科(沈阳,110044)
Author(s):
GONG Shuyi1 WANG Jingxu1 MU Shengkai1
1Department of Ridge Column Surgery,Shenyang Orthopaedics Hospital,Shenyang 110044,China.
关键词:
强直性脊柱炎 滑膜成纤维细胞 成骨分化 信号通路
Keywords:
ankylosing spondylitis synovial fibroblasts osteogenic differentiation notch signaling pathway
分类号:
R-33
文献标志码:
A
摘要:
目的:探讨miRNA-34a对强直性脊柱炎(AS)滑膜成纤维细胞成骨分化的影响及其机制。方法:将滑膜成纤维细胞分为正常组(来自创伤性骨折患者的细胞)、AS对照组(来自AS患者的细胞)、AS+NC组(转染阴性对照并给予转化生长因子-β1(TGF-β1)和 骨形态发生蛋白2(BMP-2)处理AS细胞)和AS+miRNA-34a寡核苷酸模拟物(miRNA-34a mimics)组(转染miRNA-34a mimics并给予TGF-β1和 BMP-2处理AS细胞),采用实时-PCR检测各组细胞中miRNA-34a和成骨相关基因碱性磷酸酶(ALP)、骨钙素(OCN)、Runt相关转录因子2(Runx2)mRNA以及Notch信号通路的Notch1受体与其下游靶基因Hes1 mRNA的表达水平; 将Notch信号通路激活剂rhNF-κB加入含miRNA-34a mimics的细胞中,观察ALP、OCN和Runx2 mRNA的表达变化。结果:与正常组相比,AS对照组和AS+NC组细胞中miRNA-34a表达降低,ALP、OCN、Runx2、Notch1和Hes1 mRNA的表达水平均明显升高(P<0.05); 与AS+NC组相比,AS+miRNA-34a mimics组细胞中miRNA-34a表达升高,而ALP、OCN、Runx2、Notch1和Hes1 mRNA的表达水平均明显降低(P<0.05)。给予rhNF-κB作用后,miRNA-34a mimics对ALP、OCN和Runx2 mRNA的抑制作用减弱。结论:miRNA-34a可通过调控Notch信号通路抑制AS滑膜成纤维细胞的成骨分化能力。
Abstract:
Objective:To investigate the efficacy of miRNA-34a on osteogenic differentiation of ankylosing spondylitis(AS)synovial fibroblasts and its mechanism.Methods:Synovial fibroblasts were divided into normal group(cells from patients with traumatic fractures),AS control group(cells from patients with AS),AS+NC group(transfection negative control and treatment of AS cells with TGF-β1 and BMP-2)and AS + miRNA-34a mimics group(transfection of miRNA-34a mimics and treatment of AS cells with TGF-β1 and BMP-2).The expression levels of miRNA-34a and osteogenesis-related genes ALP,OCN,Runx2 mRNA,as well as Notch signaling pathway Notch1 receptor and its downstream target gene Hes1 mRNA in the cells of each group were detected by RT-PCR.The Notch signaling pathway activator rhNF-κB was added into the cells containing miRNA-34a mimics,and the expression changes of ALP,OCN and Runx2 mRNA were observed.Results:Compared with the normal group,the expression of miRNA-34a in AS control group and AS+NC group was decreased,and the expression levels of ALP,OCN,Runx2,Notch1 and Hes1 mRNA were significantly increased(P<0.05).Compared with AS+NC group,the expression of miRNA-34a in AS+miRNA-34a mimics group was increased,while the expression levels of ALP,OCN,Runx2,Notch1 and Hes1 mRNA were significantly decreased(P<0.05).The inhibitory efficacy of miRNA-34a mimics on ALP,OCN and Runx2 mRNA were reversed after giving rhNF-κB.Conclusion:miRNA-34a can inhibit the osteogenic differentiation of AS synovial fibroblasts by regulating the Notch signaling pathway.

参考文献/References:

[1] 郭洪録,郭晓利,李力毅,等.表没食子儿茶素没食子酸对强直性脊柱炎大鼠Th1/Th2免疫平衡,软骨细胞凋亡的影响[J].郑州大学学报(医学版),2020,55(5):676-681.
[2] 包乌吉斯古冷,赵君,刘睿.补肾清热汤联合中药外敷治疗肾虚湿热型强直性脊柱炎的效果观察[J].实用临床医药杂志,2019,23(18):54-57.
[3] 杜志峰,李振彬.强直性脊柱炎疾病活动相关细胞因子分析[J].河北医学,2019,25(11):173-176.
[4] 勾志静,耿良.补肾强脊颗粒联合塞来昔布对强直性脊柱炎成纤维细胞抗骨化作用及BMP/Smad信号通路的影响[J].陕西中医,2018,39(9):1194-1197.
[5] AKKOUCH A, ELIASON S, SWEAT M E,et al.Enhancement of microRNA-200c on osteogenic differentiation and bone regeneration by targeting Sox2-mediated Wnt signaling and Klf4[J].Hum Gene Ther,2019,30(11):1405-1418.
[6] 王贵玲,杨谛,郭佳杰,等.MicroRNA 34a-5p对成骨细胞炎症反应及分化的影响[J].口腔医学研究,2017,33(11):1139-1142.
[7] 袁明权,王博,王秋霞,等.补肾中药治疗强直性脊柱炎临床疗效Meta分析[J].西部中医药,2020,33(11):76-85.
[8] TANG S L,HUANG Q H,WU L G,et al.MiR-124 regulates osteoblast differentiation through GSK-3β in ankylosing spondylitis[J].Eur Rev Med Pharmacol Sci,2018,22(20):6616-6624.
[9] 王亚寒,罗建平,王小刚,等.微小RNA-145靶向Notch通路抑制人韧带成纤维细胞向成骨细胞分化[J].中华实验外科杂志,2017,34(11):1828-1831.
[10] IWAMOTO N, FUKUI S, TAKATANI A,et al.Osteogenic differentiation of fibroblast-like synovial cells in rheumatoid arthritis is induced by microRNA-218 through a ROBO/Slit pathway[J].Arthritis Res Ther,2018,20(1):189-199.
[11] SHEN Y,LIU Y,GAO H,et al.N-Acetyl-L-leucine-polyethylenimine-mediated miR-34a delivery improves osteogenesis and bone formation in vitro and in vivo[J].Rsc Advances,2018,8(15):8080-8088.
[12] YU W W,ZHENG Y,YANG Z J,et al.N-AC-l-Leu-PEI-mediated miR-34a delivery improves osteogenic differentiation under orthodontic force[J].Oncotarget,2017,8(66):110460-110473.
[13] XIN W,WANG X,ZHANG W,et al.Tumor necrosis factor-α inhibits bone marrow stem cell differentiation into osteoblasts by downregulating microRNA-34a expression[J].Ann Clin Lab Sci,2019,49(3):324-329.
[14] 程孟文,周毅.MiR-34a在牙周膜细胞成骨向分化中的作用[J].口腔医学研究,2017,33(9):928-932.
[15] 胡通,苑迎娇,李文静,等.BMP-2对大鼠延迟再植牙牙周膜愈合影响的实验研究[J].河北医科大学学报,2018,39(12):1411-1414.
[16] 晋瑞,李嫚,雷喆,等.转化生长因子-β1对MC3T3-E1小鼠成骨细胞骨形成的影响[J].郑州大学学报(医学版),2018,53(3):378-381.
[17] 张宇博,冯华明,黄笃,等.老年髋部骨折患者骨密度与骨碱性磷酸酶、Ⅰ型胶原羧基端前肽、Ⅰ型胶原羧基端交联肽的相关性[J].实用临床医药杂志,2019,23(3):20-23.
[18] 才忠民,王欢,尚平,等.前列腺素E2诱导大鼠骨髓间充质干细胞成骨分化过程中p38 MAPK信号通路蛋白的表达[J].郑州大学学报(医学版),2020,55(1):61-65.
[19] IYYANAR P, THANGARAJ M P, EAMES B F,et al.Htra1 is a novel transcriptional target of Runx2 that promotes osteogenic differentiation[J].Cell Physiol Biochem,2019,53(5):832-850.
[20] BAGHERI L, PELLATI A, RIZZO P,et al.Notch pathway is active during osteogenic differentiation of human bone marrow mesenchymal stem cells induced by pulsed electromagnetic fields[J].J Tissue Eng Regen Med,2018,12(2):304-315.

备注/Memo

备注/Memo:
基金项目:辽宁省自然科学基金指导计划项目(20180550704)
更新日期/Last Update: 1900-01-01