...
首页> 外文期刊>Bone >Effect of lentiviral vector overexpression alpha-calcitonin gene-related peptide on titanium implant osseointegration in alpha-CGRP-deficient mice
【24h】

Effect of lentiviral vector overexpression alpha-calcitonin gene-related peptide on titanium implant osseointegration in alpha-CGRP-deficient mice

机译:慢病毒载体过表达α-降钙素基因相关肽对α-CGRP缺陷小鼠钛植入骨整合的影响

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

alpha-Calcitonin gene-related peptide (alpha-CGRP) plays a significant pathophysiological role in bone development, metabolism and remodeling around dental implants. However, the half-life of alpha-CGRP in plasma is only 10 min, which affects its long-time application and an alternative approach should be developed to deliver alpha-CGRP over long periods of time. The aim of this study is to investigate whether a lentiviral alpha-CGRP overexpression vector system can express this target-gene longer at peri-implant sites, thus enhancing osseointegration. Animals were divided to the following groups: alpha-CGRP(-/-), alpha-CGRP(-/-) with lentivirus transfection and alpha-CGRP(+/+) mice. MS Spectrum imaging observations identified the successful transfection of alpha-CGRP around experimental implants inserted in the femurs at 5 days after injection. Histomorphometrical analysis indicated an increase of bone-implant contact (BIC) at 1-month healing in the transfection group. Moreover, real-time RT-PCR and western blot results of bone-related markers Runx2, Osterix, and BSP levels elevated in lentivirus-transfected mice at 21 days, compared to the untreated alpha-CGRP(-/-) mice. There was no significant difference between the transfection group and alpha-CGRP(+/+) group. Further alpha-CGRP protein detection confirmed the persistent expression of this transgene at 21 days post-operatively. These results suggest that this lentiviral vector system expresses alpha-CGRP in an effective, appropriate and sustained manner, which might have a potential application in enhancing titanium implant osseointegration. (C) 2016 Elsevier Inc. All rights reserved.
机译:α-降钙素基因相关的肽(α-CGRP)在骨骼发育,新陈代谢和牙科植入物周围重塑中起着显着的病理生理作用。然而,血浆中α-cgrp的半衰期仅为10分钟,这影响其长期应用,并且应该开发一种替代方法来在长时间内提供alpha-cgrp。本研究的目的是研究慢病毒α-CGRP过表达载体系统是否能够在PERI植入部位表达该靶基因,从而增强骨整合。将动物分为以下基团:α-CGRP( - / - ),具有慢病毒转染和α-CGRP(+ / +)小鼠的α-CGRP( - / - )。 MS谱成像观察结果确定了在注射后5天内在插入股骨中的实验植入物周围的α-CGRP成功转染。组织素仪分析表明在转染组中1个月愈合的骨植入触点(BIC)增加。此外,与未处理的α-CGRP( - / - )小鼠相比,在慢病毒转染小鼠中,实时RT-PCR和Western runx2,Osterix和BSP水平的实时RT-PCR和Western印迹结果。转染组和α-CGRP(+ / +)组之间没有显着差异。此外,α-CGRP蛋白质检测证实了可操作后21天内转基因的持续表达。这些结果表明,该慢病毒载体系统以有效,适当和持续的方式表达α-CGRP,其可能在增强钛植入骨整合方面具有潜在的应用。 (c)2016年Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号