Spinal Cord Injury Center, Heidelberg University Hospital, Germany.
Exp Neurol. 2012 May;235(1):62-9. doi: 10.1016/j.expneurol.2011.01.015. Epub 2011 Jan 31.
During the past decades, new insights into mechanisms that limit plasticity and functional recovery after spinal cord injury have spurred the development of novel approaches to enhance axonal regeneration and rearrangement of spared circuitry. Gene therapy may provide one means to address mechanisms that underlie the insufficient regenerative response of injured neurons and can also be used to identify factors important for axonal growth. Several genetic approaches aimed to modulate the environment of injured axons, for example by localized expression of growth factors, to enhance axonal sprouting and regeneration and to guide regenerating axons towards their target have been described. In addition, genetic modification of injured neurons via intraparenchymal injection, or via retrograde transport of viral vectors has been used to manipulate the intrinsic growth capacity of injured neurons. In this review we will summarize some of the progress and limitations of cell transplantation and gene therapy to enhance axonal bridging and regeneration across a lesion site, and to maximize the function, collateral sprouting and connectivity of spared axonal systems.
在过去的几十年中,对限制脊髓损伤后可塑性和功能恢复的机制的新认识促使人们开发了新的方法来增强轴突再生和保留电路的重新排列。基因治疗可能是解决损伤神经元再生反应不足的机制的一种手段,也可用于鉴定对轴突生长重要的因素。已经描述了几种旨在调节损伤轴突环境的遗传方法,例如通过局部表达生长因子来增强轴突发芽和再生,并引导再生轴突向其靶标。此外,通过脑内注射或逆行运输病毒载体对损伤神经元进行基因修饰,已被用于操纵损伤神经元的内在生长能力。在这篇综述中,我们将总结一些细胞移植和基因治疗的进展和局限性,以增强损伤部位的轴突桥接和再生,并最大限度地提高保留轴突系统的功能、侧支发芽和连接性。