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首页> 外文期刊>Neuroscience Research: The Official Journal of the Japan Neuroscience Society >Nonviral HVJ (hemagglutinating virus of Japan) liposome-mediated retrograde gene transfer of human hepatocyte growth factor into rat nervous system promotes functional and histological recovery of the crushed nerve.
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Nonviral HVJ (hemagglutinating virus of Japan) liposome-mediated retrograde gene transfer of human hepatocyte growth factor into rat nervous system promotes functional and histological recovery of the crushed nerve.

机译:非病毒HVJ(日本血凝病毒)脂质体介导的人类肝细胞生长因子逆行基因转移到大鼠神经系统中,可促进神经压迫的功能和组织学恢复。

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摘要

Hepatocyte growth factor (HGF) is well known to be involved in many biological functions, such as organ regeneration and angiogenesis, and to exert neurotrophic effects on motor, sensory, and parasympathetic neurons. In this study, we gave repeated intramuscular injections of the human HGF gene, using nonviral HVJ (hemagglutinating virus of Japan) liposome method, to examine whether transfection of the rat nervous system with this gene is able to exert neurotrophic effects facilitating recovery of a crushed nerve. The expression of HGF protein and HGF mRNA indicated that gene transfer into the nervous system did occur via retrograde axonal transport. At 4 weeks after crush, electrophysiological examination of the crushed nerve showed a significantly shorter mean latency and a significantly greater mean maximum M-wave amplitude with repeated injections of HGF gene. Furthermore, histological findings showed that the mean diameter of the axons, the axon number and the axon population were significantly larger in the group with repeated injections of HGF gene. The above results show that repeated human HGF gene transfer into the rat nervous system is able to promote crushed-nerve recovery, both electrophysiologically and histologically, and suggest that HGF gene transfer has potential for the treatment of crushed nerve.
机译:众所周知,肝细胞生长因子(HGF)参与许多生物学功能,例如器官再生和血管生成,并对运动,感觉和副交感神经元产生神经营养作用。在这项研究中,我们使用非病毒性HVJ(日本血凝病毒)脂质体方法反复进行了人类HGF基因的肌肉注射,以检查用该基因转染大鼠神经系统是否能够发挥神经营养作用,从而促进压碎物的恢复。神经。 HGF蛋白和HGF mRNA的表达表明基因转移确实通过逆行轴突运输发生到神经系统中。挤压后4周,对神经的电生理检查显示,重复注射HGF基因后,平均潜伏期明显缩短,平均最大M波幅值明显升高。此外,组织学结果显示,在重复注射HGF基因的组中,轴突的平均直径,轴突数目和轴突群体显着更大。以上结果表明,人HGF基因的反复转移进入大鼠神经系统能够在电生理和组织学上促进神经粉碎性恢复,并且表明HGF基因转移具有治疗神经粉碎性的潜力。

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