School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.
IEEE Trans Biomed Eng. 2011 Jul;58(7):1900-6. doi: 10.1109/TBME.2010.2103075. Epub 2010 Dec 30.
One of the grand challenges in neuroengineering is to stimulate regeneration after central nervous system (CNS) or peripheral nervous system (PNS) injury to restore function. The state of the art today is that PNS injuries heal to a limited extent, whereas CNS injuries are largely intractable to regeneration. In this context, we examine the underlying biochemical and cellular constraints on endogenous healing of neural tissues. Identification and characterization of endogenous "rate-limiting" processes that constrain regeneration would allow one to craft solutions to overcome critical impediments for accelerated healing. It is increasingly evident that biochemical pathways triggered by the nature and duration of injury-triggered inflammatory response may determine the endogenous constraints and subsequently determine regenerative fate. In this paper, critical endogenous constraints of PNS and CNS regeneration are identified, and the effects of modulating the phenotypes of immune cells on neuronal regeneration are discussed.
神经工程学的重大挑战之一是在中枢神经系统 (CNS) 或周围神经系统 (PNS) 损伤后刺激再生,以恢复功能。目前的技术水平是,PNS 损伤在一定程度上可以愈合,而 CNS 损伤则在很大程度上难以再生。在这种情况下,我们研究了内源性神经组织愈合的潜在生化和细胞限制。鉴定和表征限制再生的内源性“限速”过程,将有助于制定解决方案来克服加速愈合的关键障碍。越来越明显的是,由损伤引发的炎症反应的性质和持续时间触发的生化途径可能决定内源性限制,并随后决定再生命运。本文确定了 PNS 和 CNS 再生的关键内源性限制,并讨论了调节免疫细胞表型对神经元再生的影响。