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作 者:杨平 雷智杰 于江林 邱旭升 陈一心 戚晓阳[1,3] Yang Ping;Lei Zhijie;Yu Jianglin;Qiu Xusheng;Chen Yixin;Qi Xiaoyang(Department of Orthopaedics,Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine,Nanjing 210000,China;Department of Orthopaedics,Nanjing Drum Tower Hospital Clinical College of Jiangsu University,Nanjing 210000,China;Department of Orthopaedics,Nanjing Drum Tower Hospital,the Affiliated Hospital of Nanjing University Medical School,Nanjing 210000,China)
机构地区:[1]南京中医药大学鼓楼临床医学院骨科,江苏南京210000 [2]江苏大学鼓楼临床医学院骨科,江苏南京210000 [3]南京大学医学院附属鼓楼医院骨科,江苏南京210000
出 处:《实用骨科杂志》2024年第6期514-518,共5页Journal of Practical Orthopaedics
基 金:南京市卫生局重点项目(ZKX21029)。
摘 要:目的研究负载纤维蛋白原的胶原膜对大鼠股骨骨折愈合的影响及机制。方法将大鼠股骨骨折模型随机分为三组,分别为对照组、胶原膜组、负载纤维蛋白原胶原膜组。术后第8周取患侧股骨行Micro-CT分析骨痂形成情况。大鼠原代骨髓间充质干细胞(bone marrow mesenchymal stem cell,BMSC)分为成骨对照组、纤维蛋白原+成骨诱导组、纤维蛋白原+PNU-74654+成骨诱导组。BCIP/NBT染色法检测BMSC的碱性磷酸酶(alkaline phosphatases,ALP)水平,Wsetern blot分别检测成骨指标Ⅰ型胶原蛋白(collagenⅠ,COL-1)、ALP、Runt相关转录因子2(Runt-related transcription factor 2,RUNX2)、β-Catenin的蛋白表达。结果Micro-CT显示术后2个月大鼠股骨骨折端的骨痂形成量,负载纤维蛋白原胶原膜组显著多于胶原膜组和对照组。ALP染色和Western blot结果显示纤维蛋白原能够促进成骨表,且纤维蛋白原通过激活Wnt/β-Catenin信号通路上调成骨指标的表达,而使用PNU-74654(Wnt/β-Catenin通路抑制剂)后成骨指标表达显著下降(P<0.05)。结论负载纤维蛋白原的胶原膜能加速骨折愈合。纤维蛋白原通过激活Wnt/β-Catenin信号通路能促进BMSC成骨分化。Objective To investigate the effect and mechanism of the collagen membrane loaded with fibrinogen on healing of femoral fractures in rats.Methods The rat femur fracture models were randomly divided into three groups:control group,collagen membrane group,and fibrinogen-loaded collagen membrane group.At 8 weeks post-surgery,the affected femurs of the rats were analyzed using Micro-CT scanning to assess callus formation.Primary bone marrow mesenchymal stem cells(BMSC)were divided into osteogenic control group,fibrinogen+osteogenic induction group,fibrinogen+PNU-74654+osteogenic induction group.BCIP/NBT staining was used to detect the level of alkaline phosphatases(ALP)in BMSC.Wsetern blot was used to detect the protein expression of osteogenic markers,collagenⅠ(COL-1),ALP,Runt-related transcription factor 2(RUNX2),andβ-Catenin.Results The Micro-CT analysis revealed that at 2 months post-surgery,the fibrinogen-loaded collagen membrane group exhibited significantly higher levels of callus formation compared to the control group.ALP staining and Western blot results further indicated that fibrinogen promotes osteogenesis by upregulating the expression of osteogenic markers through the activation of the Wnt/β-Catenin signaling pathway.However,when PNU-74654(a Wnt/β-Catenin inhibitor)was utilized,the expression of osteogenic markers was significantly reduced(P<0.05).Conclusion The fibrinogen-loaded collagen membrane can accelerate femur fracture healing in rats,and fibrinogen accomplishes this by promoting osteogenic differentiation of bone marrow mesenchymal stem cells(BMSCs)via the activation of the Wnt/β-Catenin signaling pathway.
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