• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

BMP7 基因修饰的 BMSCs 与负载型组织工程骨增强山羊股骨缺损的愈合。

Enhanced healing of goat femur-defect using BMP7 gene-modified BMSCs and load-bearing tissue-engineered bone.

机构信息

Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, No. 639 Zhi Zhaoju Road, Shanghai 200011, P. R. China.

出版信息

J Orthop Res. 2010 Mar;28(3):412-8. doi: 10.1002/jor.20973.

DOI:10.1002/jor.20973
PMID:19725097
Abstract

Segmental defect regeneration is still a clinical challenge. In this study, we investigated the feasibility of bone marrow stromal cells (BMSCs) infected with adenoviral vector containing the bone morphogenetic protein 7 gene (AdBMP7) and load-bearing to enhance bone regeneration in a critically sized femoral defect in the goat model. The defects were implanted with AdBMP7-infected BMSCs/coral (BMP7 group) or noninfected BMSCs/coral (control group), respectively, stabilized with an internal fixation rod and interlocking nails. Bridging of the segmental defects was evaluated by radiographs monthly, and confirmed by biomechanical tests. Much callus was found in the BMP7 group, and nails were taken off after 3 months of implantation, indicating that regenerated bone in the defect can be remodeled by load-bearing, whereas after 6 months in control group. After load-bearing, it is about 5 months; the mechanical property of newly formed bone in the BMP7 group was restored, but 8 months in control group. Our data suggested that the BMP7 gene-modified BMSCs and load-bearing can promote bone regeneration in segmental defects.

摘要

节段性缺损的再生仍然是一个临床挑战。在这项研究中,我们研究了感染含有骨形态发生蛋白 7 基因的腺病毒载体的骨髓基质细胞(BMSCs)和负载以增强山羊模型中临界尺寸股骨缺损骨再生的可行性。将 AdBMP7 感染的 BMSCs/珊瑚(BMP7 组)或未感染的 BMSCs/珊瑚(对照组)分别植入缺陷部位,并用内部固定杆和锁定钉固定。通过每月进行 X 线评估和生物力学测试来确认节段性缺损的桥接。在 BMP7 组中发现了大量骨痂,植入 3 个月后取出了钉子,表明缺损部位的再生骨可以通过负重进行重塑,而在对照组中则需要 6 个月。在负重后,大约需要 5 个月;BMP7 组中新形成的骨的机械性能得以恢复,但对照组则需要 8 个月。我们的数据表明,BMP7 基因修饰的 BMSCs 和负载可以促进节段性缺损中的骨再生。

相似文献

1
Enhanced healing of goat femur-defect using BMP7 gene-modified BMSCs and load-bearing tissue-engineered bone.BMP7 基因修饰的 BMSCs 与负载型组织工程骨增强山羊股骨缺损的愈合。
J Orthop Res. 2010 Mar;28(3):412-8. doi: 10.1002/jor.20973.
2
Tissue-engineered bone repair of goat-femur defects with osteogenically induced bone marrow stromal cells.用成骨诱导的骨髓基质细胞进行山羊股骨缺损的组织工程骨修复。
Tissue Eng. 2006 Mar;12(3):423-33. doi: 10.1089/ten.2006.12.423.
3
[The feasibility of adenoviral co-transduction of BMP2 and BMP7 for the expression of recombinant human BMP2/7 heterodimer in rat bone marrow mesenchymal stem cells].腺病毒共转导BMP2和BMP7在大鼠骨髓间充质干细胞中表达重组人BMP2/7异二聚体的可行性
Zhonghua Zheng Xing Wai Ke Za Zhi. 2016 Mar;32(2):125-29.
4
Repair of goat tibial defects with bone marrow stromal cells and beta-tricalcium phosphate.用骨髓基质细胞和β-磷酸三钙修复山羊胫骨缺损
J Mater Sci Mater Med. 2008 Jun;19(6):2367-76. doi: 10.1007/s10856-007-3348-3. Epub 2007 Dec 25.
5
[Effect of adeno-BMP7 transfection on osteogenesis of BMSCs].腺病毒介导的骨形态发生蛋白7转染对骨髓间充质干细胞成骨作用的影响
Zhonghua Zheng Xing Wai Ke Za Zhi. 2006 Jan;22(1):59-62.
6
Large-scale bicortical skull bone regeneration using ex vivo replication-defective adenoviral-mediated bone morphogenetic protein-2 gene-transferred bone marrow stromal cells and composite biomaterials.采用体外复制缺陷型腺病毒介导的骨形态发生蛋白-2 基因转染骨髓基质细胞和复合生物材料进行大规模双皮质颅骨骨再生。
Neurosurgery. 2009 Dec;65(6 Suppl):75-81; discussion 81-3. doi: 10.1227/01.NEU.0000345947.33730.91.
7
Repair of canine mandibular bone defects with bone marrow stromal cells and coral.用骨髓基质细胞和珊瑚修复犬下颌骨缺损。
Tissue Eng Part A. 2010 Apr;16(4):1385-94. doi: 10.1089/ten.TEA.2009.0472.
8
NELL1 promotes high-quality bone regeneration in rat femoral distraction osteogenesis model.NELL1 促进大鼠股骨牵张成骨模型中的高质量骨再生。
Bone. 2011 Mar 1;48(3):485-95. doi: 10.1016/j.bone.2010.10.166. Epub 2010 Oct 17.
9
Comparing the osteogenic potential of bone marrow and tendon-derived stromal cells to repair a critical-sized defect in the rat femur.比较骨髓和肌腱来源的基质细胞修复大鼠股骨临界尺寸缺损的成骨潜能。
J Tissue Eng Regen Med. 2017 Jul;11(7):2014-2023. doi: 10.1002/term.2097. Epub 2015 Oct 29.
10
Healing of critically sized femoral defects, using genetically modified mesenchymal stem cells from human adipose tissue.使用来自人脂肪组织的基因改造间充质干细胞修复临界尺寸的股骨缺损。
Tissue Eng. 2005 Jan-Feb;11(1-2):120-9. doi: 10.1089/ten.2005.11.120.

引用本文的文献

1
Gene Therapy for Regenerative Medicine.用于再生医学的基因治疗
Pharmaceutics. 2023 Mar 6;15(3):856. doi: 10.3390/pharmaceutics15030856.
2
Musculoskeletal tissue engineering: Adipose derived stromal cell implementation for the treatment of osteoarthritis.肌肉骨骼组织工程学:脂肪来源基质细胞在骨关节炎治疗中的应用。
Biomaterials. 2022 Jul;286:121544. doi: 10.1016/j.biomaterials.2022.121544. Epub 2022 May 6.
3
Clinical Applications of Cell-Scaffold Constructs for Bone Regeneration Therapy.细胞-支架构建物在骨再生治疗中的临床应用。
Cells. 2021 Oct 8;10(10):2687. doi: 10.3390/cells10102687.
4
Bone Morphogenetic Protein-2 Rapidly Heals Two Distinct Critical Sized Segmental Diaphyseal Bone Defects in a Porcine Model.骨形态发生蛋白-2 可快速治愈猪模型中两种不同的临界尺寸节段骨干骨缺损。
Mil Med. 2023 Jan 5;188(1-2):117-124. doi: 10.1093/milmed/usab360.
5
Systematic Review of the Preclinical Technology Readiness of Orthopedic Gene Therapy and Outlook for Clinical Translation.骨科基因治疗临床前技术成熟度的系统评价及临床转化前景
Front Bioeng Biotechnol. 2021 Mar 17;9:626315. doi: 10.3389/fbioe.2021.626315. eCollection 2021.
6
Internal Fixation Construct and Defect Size Affect Healing of a Translational Porcine Diaphyseal Tibial Segmental Bone Defect.内固定结构和缺损大小影响猪胫骨骨干节段性骨缺损的愈合。
Mil Med. 2021 Nov 2;186(11-12):e1115-e1123. doi: 10.1093/milmed/usaa516.
7
Enhancement of osteogenesis of rabbit bone marrow derived mesenchymal stem cells by transfection of human BMP-2 and EGFP recombinant adenovirus via Wnt signaling pathway.通过Wnt信号通路转染人BMP-2和EGFP重组腺病毒增强兔骨髓间充质干细胞的成骨作用
Exp Ther Med. 2018 Nov;16(5):4030-4036. doi: 10.3892/etm.2018.6735. Epub 2018 Sep 13.
8
Tissue Engineering and Cell-Based Therapies for Fractures and Bone Defects.用于骨折和骨缺损的组织工程与基于细胞的疗法。
Front Bioeng Biotechnol. 2018 Jul 31;6:105. doi: 10.3389/fbioe.2018.00105. eCollection 2018.
9
Transplantation of periodontal ligament cell sheets expressing human β‑defensin‑3 promotes anti‑inflammation in a canine model of periodontitis.表达人β防御素-3 的牙周膜细胞片的移植促进牙周炎犬模型中的抗炎作用。
Mol Med Rep. 2017 Nov;16(5):7459-7467. doi: 10.3892/mmr.2017.7514. Epub 2017 Sep 19.
10
The Role of Three-Dimensional Scaffolds in Treating Long Bone Defects: Evidence from Preclinical and Clinical Literature-A Systematic Review.三维支架在治疗长骨缺损中的作用:临床前和临床文献的证据——系统评价。
Biomed Res Int. 2017;2017:8074178. doi: 10.1155/2017/8074178. Epub 2017 Aug 9.