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骨形态发生蛋白4电穿孔基因转移诱导异位骨形成的基因表达分析

Gene expression analysis of ectopic bone formation induced by electroporatic gene transfer of BMP4.

作者信息

Kotajima Satoshi, Kishimoto Koshi N, Watanuki Munenori, Hatori Masahito, Kokubun Shoichi

机构信息

Department of Orthopaedic Surgery, Tohoku University School of Medicine, Sendai, Miyagi, Japan.

出版信息

Ups J Med Sci. 2006;111(2):231-41. doi: 10.3109/2000-1967-044.

Abstract

Implantation of bone morphogenetic protein (BMP) using a carrier or by BMP gene transfer into rodent muscle can induce bone formation. Implanted BMP becomes bioactive immediately after implantation. In BMP gene transfer, there is a time-lag between the secretion of gene products and bone formation. We analyzed the gene expression of chondrogenic and osteogenic specific markers in the process of ectopic bone formation by using semi-quantitative RT-PCR. A plasmid vector containing mouse BMP4 gene (pCAGGS-BMP4) was transferred into the gastrocnemius muscles of mice using electroporation. Histological examination revealed the process of endochondral bone formation in the pCAGGS-BMP4 transferred muscles. As chondrogenic markers, aggrecan gene maximal expression was detected on day 7 and decreased by day 14, and for collagen X the gene maximal expression was on day 10. As osteogenic markers, osteocalcin (OCN), bone sialoprotein (BSP) and osteopontin (OPN) gene expressions were clearly detected from day 10 and then increased by day 14. In conclusion, the present study proved that ectopic bone formation by BMP4 gene transfer into the muscle induced endochondral ossification that corresponded well with that to that by implantation of demineralized bone matrix.

摘要

使用载体植入骨形态发生蛋白(BMP)或通过BMP基因转移至啮齿动物肌肉中可诱导骨形成。植入的BMP在植入后立即具有生物活性。在BMP基因转移中,基因产物分泌与骨形成之间存在时间滞后。我们通过半定量RT-PCR分析了异位骨形成过程中软骨生成和成骨特异性标志物的基因表达。使用电穿孔法将含有小鼠BMP4基因的质粒载体(pCAGGS-BMP4)转移到小鼠的腓肠肌中。组织学检查揭示了pCAGGS-BMP4转移肌肉中软骨内骨形成的过程。作为软骨生成标志物,聚集蛋白聚糖基因在第7天检测到最大表达,并在第14天下降,而胶原蛋白X基因的最大表达在第10天。作为成骨标志物,骨钙素(OCN)、骨唾液蛋白(BSP)和骨桥蛋白(OPN)基因表达从第10天开始清晰检测到,然后在第14天增加。总之,本研究证明,通过将BMP4基因转移到肌肉中进行异位骨形成可诱导软骨内骨化,这与植入脱矿骨基质诱导的骨化情况非常吻合。

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