Kawai Mariko, Bessho Kazuhisa, Maruyama Hiroki, Miyazaki Jun-Ichi, Yamamoto Toshio
Department of Oral Morphology, Okayama University Graduate School of Medicine and Dentistry, Okayama, Japan.
Anat Rec A Discov Mol Cell Evol Biol. 2005 Dec;287(2):1264-71. doi: 10.1002/ar.a.20245.
It has been generally accepted that bone morphogenetic protein-2 (BMP-2) can induce osteogenesis in skeletal muscles via endochondral ossification. However, it is not clear how the ossification process occurs after the BMP-2 gene transfer to skeletal muscles in rats using in vivo electroporation. In this study, we evaluated the ossification process by BMP-2 gene transfer using in vivo electroporation. The gastrocnemius muscles of Wistar rats were injected with human BMP-2 gene expression vector (pCAGGS-BMP-2), followed by electroporation under the condition of 100 V, 50 msec per 1 sec, x8. Light and electron microscopic and radiographic analyses were performed at 1, 3, 5, 7, and 10 days after treatment. At 7 days, no sign of cartilage and/or bone formation was detected. However, at 10 days after in vivo electroporation, soft X-ray analysis revealed small lucent areas around the plasmid-injected region. Clusters of both cartilage tissues, leading to endochondral ossification and intramembranous bones of various sizes, were observed between muscle fibers. RT-PCR detected osteocalcin mRNA, showing bone formation at 10 days. Our findings strongly suggest that BMP-2 gene transfer using in vivo electroporation induces not only endochondral ossification but also intramembranous ossification.
人们普遍认为骨形态发生蛋白-2(BMP-2)可通过软骨内成骨诱导骨骼肌发生骨生成。然而,尚不清楚使用体内电穿孔法将BMP-2基因导入大鼠骨骼肌后,骨化过程是如何发生的。在本研究中,我们评估了使用体内电穿孔法进行BMP-2基因转移后的骨化过程。向Wistar大鼠的腓肠肌注射人BMP-2基因表达载体(pCAGGS-BMP-2),然后在100 V、每秒50毫秒、共8次的条件下进行电穿孔。在治疗后第1、3、5、7和10天进行光镜、电镜和放射学分析。在第7天,未检测到软骨和/或骨形成的迹象。然而,在体内电穿孔后第10天,软X射线分析显示在质粒注射区域周围有小的透亮区。在肌纤维之间观察到软骨组织簇,导致软骨内成骨和各种大小的膜内骨。RT-PCR检测到骨钙素mRNA,表明在第10天有骨形成。我们的研究结果强烈表明,使用体内电穿孔法进行BMP-2基因转移不仅诱导软骨内成骨,还诱导膜内成骨。