Tom Veronica J, Houlé John D
Department of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA 19129, USA.
Exp Neurol. 2008 May;211(1):315-9. doi: 10.1016/j.expneurol.2008.01.021. Epub 2008 Feb 14.
Chondroitin sulfate proteoglycans (CSPG) within the glial scar formed after central nervous system (CNS) injury are thought to play a crucial role in regenerative failure. We previously showed that delivery of the CSPG-digesting enzyme chondroitinase ABC (ChABC) via an osmotic minipump allowed axonal regeneration and functional recovery in a peripheral nerve graft (PNG)-bridging model. In this study, we sought to overcome the technical limitations associated with minipumps by microinjecting ChABC directly into the distal lesion site in the PN bridging model. Microinjection of ChABC immediately rostral and caudal to an injury site resulted in extensive CSPG digestion. We also demonstrate that this delivery technique is relatively atraumatic and does not result in a noticeable inflammatory response. Importantly, microinjections of ChABC into the lesion site permitted more regenerating axons to exit a PNG and reenter spinal cord tissue than saline injections. These results are similar to our previous findings when ChABC was delivered via a minipump and suggest that microinjecting ChABC is an effective method of delivering the potentially therapeutic enzyme directly to an injury site.
中枢神经系统(CNS)损伤后形成的胶质瘢痕中的硫酸软骨素蛋白聚糖(CSPG)被认为在再生失败中起关键作用。我们之前表明,通过渗透微型泵递送CSPG消化酶软骨素酶ABC(ChABC)可使周围神经移植(PNG)桥接模型中的轴突再生和功能恢复。在本研究中,我们试图通过在PN桥接模型中将ChABC直接显微注射到远端损伤部位来克服与微型泵相关的技术限制。在损伤部位的头端和尾端立即显微注射ChABC导致广泛的CSPG消化。我们还证明,这种递送技术相对无创,不会引起明显的炎症反应。重要的是,与注射生理盐水相比,将ChABC显微注射到损伤部位可使更多再生轴突离开PNG并重新进入脊髓组织。这些结果与我们之前通过微型泵递送ChABC时的发现相似,表明显微注射ChABC是将潜在治疗性酶直接递送至损伤部位的有效方法。