利用非病毒BMP基因表达载体和体内电穿孔技术进行骨再生的基因治疗

RAN Pub Date : 2016-04-01 DOI:10.11159/NDDTE16.107
M. Kawai, K. Ohura
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引用次数: 0

摘要

骨形态发生蛋白(bone morphogenetic protein, BMP)重组蛋白或BMP基因转移到骨骼肌后可诱导异位骨形成。我们提出了一种新的BMP基因转移方法,即结合非病毒BMP基因表达载体和体内电穿孔。然后,我们应用该方法将BMP-2基因导入大鼠骨骼肌,在靶部位诱导异位骨形成。我们将BMP基因表达载体pCAGGS-BMP-2注射到大鼠骨骼肌中,在100电压、50 msec条件下立即电穿孔。8个脉冲。BMP基因移植21天后,骨骼肌出现异位骨形成。在BMP家族中,BMP-2/4或BMP-2/7异源二聚体比BMP-2、BMP-4或BMP-7同源二聚体具有更强的骨诱导潜能。然后,我们构建了BMP-2/7异二聚体产生的载体:pCAGGS-BMP-2/7。它没有IRES位点,因此BMP-2和BMP-7基因的表达是相等的。将pCAGGS-BMP-2/7质粒载体注入骨骼肌,立即进行体内电穿孔,在基因转移10天后快速诱导异位骨形成。为了临床应用,我们需要在低于100电压的条件下进行更安全的体内电穿孔操作。如果我们将条件设置为50电压和8脉冲,基因传递效率也会降低。但是,当我们诱导脉冲数时,它恢复了。我们评估了适当的电压和脉冲数与100电压相同的基因转移效率。我们尝试将该基因转移系统应用于低于50电压条件下的牙槽骨再生。由于牙周病或外伤引起的牙槽骨缺损,常用骨修复材料和自体骨移植。但是,这些疗法有时对患者有一些风险,比如感染或骨折。我们开发的骨再生基因治疗系统将更加安全,减轻患者负担。
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Gene Therapy for Bone Regeneration using Non-viral BMP Gene Expression Vector and in vivo Electroporation
It is well known that bone morphogenetic protein (BMP) induces ectopic bone formation when the recombinant protein or BMP gene is transferred into the skeletal muscle. We developed a novel method for BMP gene transfer, which is combination with nonviral BMP gene expression vector and in vivo electroporation. Then, we applied this method to transfer BMP-2 gene into the skeletal muscles of rats and induced the ectopic bone formation in the target sites. We injected BMP gene expression vector, pCAGGS-BMP-2, in the skeletal muscles of rats and immediately electroporated under the conditions of 100 voltage, 50 msec., and 8 pulses. We found the ectopic bone formation in the skeletal muscles 21 days after BMP gene transfer. In the BMP family, BMP-2/4 or BMP-2/7 heterodimer has stronger potential for bone induction compared with BMP-2, BMP-4 or BMP-7 homodimer. Then, we constructed BMP-2/7 heterodimer produced vector: pCAGGS-BMP-2/7. It has no IRES site, therefore each of BMP-2 and BMP-7 gene expression is equal. When we injected pCAGGS-BMP-2/7 plasmid vector in the skeletal muscles and immediately performed in vivo electroporation, the ectopic bone formation was induced quickly on 10 days after gene transfer. For clinical application, we need more safe procedure on in vivo electroporation under the condition of lower voltage than 100 voltage. If we set the condition: 50 voltage and 8 pulses, the efficiency of gene transfer also reduced. But, when we induced pulse number, it recovered. We evaluated proper voltage and pulse number as the same gene transfer efficiency of 100 voltage. We tried to apply this gene transfer system for alveolar bone regeneration under the condition less 50 voltage. We often use bone prosthetic material and autogenous bone graft for alveolar bone defect caused by periodontal disease or trauma. But, these therapies sometimes have some risk for patients such as infection or fractures. Our developed gene therapy system for bone regeneration will be with more safety and with less burden on the patient.
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