• 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

在马第四掌骨截骨模型中使用编码骨形态发生蛋白-2和蛋白-7基因的腺病毒载体进行直接体内基因转移的评估。

Evaluation of direct in vivo gene transfer in an equine metacarpal IV ostectomy model using an adenoviral vector encoding the bone morphogenetic protein-2 and protein-7 gene.

作者信息

Southwood Louise L, Kawcak Christopher E, Hidaka Chisa, McIlwraith C Wayne, Werpy Natasha, Macleay Jennifer, Frisbie David D

机构信息

Department of Clinical Studies, New Bolton Center, University of Pennsylvania, Kennett Square, PA 19348, USA.

出版信息

Vet Surg. 2012 Apr;41(3):345-54. doi: 10.1111/j.1532-950X.2011.00947.x. Epub 2012 Feb 6.

DOI:10.1111/j.1532-950X.2011.00947.x
PMID:22308976
Abstract

OBJECTIVE

To evaluate gene transfer in an equine metacarpal IV (MCIV) ostectomy model using adenoviral vectors encoding the human bone morphogenetic protein-2 and protein-7 gene (Ad-BMP-2/-7).

EXPERIMENTAL ANIMALS

Healthy adult horses (n = 15).

METHODS

A plate stabilized, critical size 1.5 cm ostectomy was created in left and right MCIV. The ostectomy site was injected with either Ad-green fluorescent protein (Ad-GFP) or Ad-hBMP-2/-7 at completion of surgery; the same treatment was assigned to both the left and right forelimb of each horse (n = 5 horses/group). Bone healing was evaluated radiographically every 2 weeks for 16 weeks. Horses in a pilot study (n = 5) were used as untreated controls for radiographic evaluation to 8 weeks. After euthanasia at 16 weeks bone healing was evaluated using dual energy X-ray absorptiometry (DEXA) and histomorphometry. Data were analyzed using an ANOVA or Kruskal-Wallis test. Level of significance was P < .05.

RESULTS

At 4 and 6 weeks, the Ad-GFP group had a significantly lower percentage defect ossification compared with the untreated control group. There was no significant difference between untreated and Ad-hBMP-2/-7 groups at any time point and no significant difference in bone healing radiographically, histologically, or using DEXA between any groups at 16 weeks.

CONCLUSIONS

Ad-hBMP-2/-7 did not improve bone healing in horses at 16 weeks.

摘要

目的

在马的第四掌骨(MCIV)截骨模型中,使用编码人骨形态发生蛋白-2和蛋白-7基因的腺病毒载体(Ad-BMP-2/-7)评估基因转移情况。

实验动物

健康成年马(n = 15)。

方法

在左右MCIV上制造一个尺寸为1.5厘米的钢板固定临界大小截骨术。手术完成时,在截骨部位注射Ad-绿色荧光蛋白(Ad-GFP)或Ad-hBMP-2/-7;每匹马的左右前肢接受相同治疗(n = 5匹马/组)。每2周进行一次X线摄影评估骨愈合情况,持续16周。在一项初步研究中的马(n = 5)用作未治疗对照组,进行8周的X线摄影评估。在16周实施安乐死后,使用双能X线吸收法(DEXA)和组织形态计量学评估骨愈合情况。数据采用方差分析或Kruskal-Wallis检验进行分析。显著性水平为P < 0.05。

结果

在4周和6周时,与未治疗对照组相比,Ad-GFP组的缺损骨化百分比显著更低。在任何时间点,未治疗组和Ad-hBMP-2/-7组之间均无显著差异,且在16周时,任何组之间在X线摄影、组织学或使用DEXA评估的骨愈合方面均无显著差异。

结论

Ad-hBMP-2/-7在16周时未改善马的骨愈合情况。

相似文献

1
Evaluation of direct in vivo gene transfer in an equine metacarpal IV ostectomy model using an adenoviral vector encoding the bone morphogenetic protein-2 and protein-7 gene.在马第四掌骨截骨模型中使用编码骨形态发生蛋白-2和蛋白-7基因的腺病毒载体进行直接体内基因转移的评估。
Vet Surg. 2012 Apr;41(3):345-54. doi: 10.1111/j.1532-950X.2011.00947.x. Epub 2012 Feb 6.
2
Osteogenic gene regulation and relative acceleration of healing by adenoviral-mediated transfer of human BMP-2 or -6 in equine osteotomy and ostectomy models.腺病毒介导的人骨形态发生蛋白-2或-6在马截骨术和骨切除术模型中的成骨基因调控及愈合相对加速作用
J Orthop Res. 2008 Jun;26(6):764-71. doi: 10.1002/jor.20585.
3
Direct delayed human adenoviral BMP-2 or BMP-6 gene therapy for bone and cartilage regeneration in a pony osteochondral model.直接延迟的人腺病毒 BMP-2 或 BMP-6 基因治疗在小马骨关节模型中的骨和软骨再生。
Osteoarthritis Cartilage. 2011 Aug;19(8):1066-75. doi: 10.1016/j.joca.2011.05.007. Epub 2011 Jun 2.
4
Adenoviral-mediated transfer of human BMP-6 gene accelerates healing in a rabbit ulnar osteotomy model.腺病毒介导的人骨形态发生蛋白-6基因转移可加速兔尺骨截骨模型的愈合。
J Orthop Res. 2004 Nov;22(6):1261-70. doi: 10.1016/j.orthres.2004.03.014.
5
Comparative efficacy of dermal fibroblast-mediated and direct adenoviral bone morphogenetic protein-2 gene therapy for bone regeneration in an equine rib model.真皮成纤维细胞介导与直接腺病毒骨形态发生蛋白-2 基因治疗在马肋模型中骨再生的比较疗效。
Gene Ther. 2010 Jun;17(6):733-44. doi: 10.1038/gt.2010.13. Epub 2010 Mar 11.
6
Assessment of the mineral density and mineral content of the equine third metacarpal and first phalanx bone by dual energy x-ray absorptiometry.通过双能X线吸收法评估马第三掌骨和第一指骨的骨密度和矿物质含量。
Acta Vet Hung. 2010 Sep;58(3):317-29. doi: 10.1556/AVet.58.2010.3.5.
7
Direct percutaneous gene delivery to enhance healing of segmental bone defects.直接经皮基因递送以促进节段性骨缺损的愈合。
J Bone Joint Surg Am. 2006 Feb;88(2):355-65. doi: 10.2106/JBJS.E.00464.
8
Healing of large segmental bone defects induced by expedited bone morphogenetic protein-2 gene-activated, syngeneic muscle grafts.加速骨形态发生蛋白-2 基因激活、同种异体肌肉移植物诱导的大节段骨缺损的愈合。
Hum Gene Ther. 2009 Dec;20(12):1589-96. doi: 10.1089/hum.2009.037.
9
Synergistic effect of bone morphogenetic proteins 2 and 7 by ex vivo gene therapy in a rat spinal fusion model.骨形态发生蛋白 2 和 7 的体外基因治疗在大鼠脊柱融合模型中的协同作用。
J Bone Joint Surg Am. 2013 Sep 4;95(17):1612-9. doi: 10.2106/JBJS.L.01396.
10
Evaluation of Ad-BMP-2 for enhancing fracture healing in an infected defect fracture rabbit model.
J Orthop Res. 2004 Jan;22(1):66-72. doi: 10.1016/S0736-0266(03)00129-3.

引用本文的文献

1
Gene Therapy in Orthopaedics: Progress and Challenges in Pre-Clinical Development and Translation.骨科中的基因治疗:临床前开发与转化中的进展与挑战
Front Bioeng Biotechnol. 2022 Jun 28;10:901317. doi: 10.3389/fbioe.2022.901317. eCollection 2022.
2
Influence of a novel scaffold composed of polyurethane, hydroxyapatite, and decellularized bone particles on the healing of fourth metacarpal defects in mares.新型聚氨酯、羟基磷灰石和脱细胞骨颗粒支架对马第四掌骨缺损愈合的影响。
Vet Surg. 2021 Jul;50(5):1117-1127. doi: 10.1111/vsu.13608. Epub 2021 May 5.
3
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.
4
Genetic modification of scAAV-equine-BMP-2 transduced bone-marrow-derived mesenchymal stem cells before and after cryopreservation: An "off-the-shelf" option for fracture repair.冻存前后 scAAV-马-BMP-2 转导骨髓间充质干细胞的基因修饰:骨折修复的“即用型”选择。
J Orthop Res. 2019 Jun;37(6):1310-1317. doi: 10.1002/jor.24209. Epub 2019 Feb 21.
5
The challenges of promoting osteogenesis in segmental bone defects and osteoporosis.促进节段性骨缺损和成骨不全症中骨生成的挑战。 (注:原文中osteoporosis一般指骨质疏松症,这里可能是osteogenesis imperfecta的误写,按照正确的osteogenesis imperfecta翻译为成骨不全症,如果原文无误则按照骨质疏松症翻译,译文可改为:促进节段性骨缺损和骨质疏松症中骨生成的挑战。)
J Orthop Res. 2018 Jun;36(6):1559-1572. doi: 10.1002/jor.23845. Epub 2018 Mar 6.
6
Implant Composed of Demineralized Bone and Mesenchymal Stem Cells Genetically Modified with AdBMP2/AdBMP7 for the Regeneration of Bone Fractures in .由脱矿骨和经AdBMP2/AdBMP7基因修饰的间充质干细胞组成的植入物用于[具体部位]骨折的再生 。 (你提供的原文最后“in.”后面似乎缺少具体信息)
Stem Cells Int. 2016;2016:7403890. doi: 10.1155/2016/7403890. Epub 2016 Oct 13.
7
Gene therapy approaches to regenerating the musculoskeletal system.用于再生肌肉骨骼系统的基因治疗方法。
Nat Rev Rheumatol. 2015 Apr;11(4):234-42. doi: 10.1038/nrrheum.2015.28. Epub 2015 Mar 17.