McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania.
J Biomed Mater Res A. 2018 Feb;106(2):450-459. doi: 10.1002/jbm.a.36235. Epub 2017 Oct 23.
Peripheral nerve possesses the inherent ability to regrow and recover following injury. However, nerve regeneration is often slow and incomplete due to limitations associated with the local microenvironment during the repair process. Manipulation of the local microenvironment at the site of nerve repair, therefore, represents a significant opportunity for improvement in downstream outcomes. Macrophages and Schwann cells play a key role in the orchestration of early events after peripheral nerve injury. We describe the production, characterization, and use of an injectable, peripheral nerve-specific extracellular matrix-based hydrogel (PNSECM) for promoting modulation of the local macrophage and Schwann cell responses at the site of nerve repair in a rodent model of sciatic nerve injury. We show that PNSECM hydrogels largely maintain the matrix structure associated with normal native peripheral nerve tissue. PNSECM hydrogels were also found to promote increased macrophage invasion, higher percentages of M2 macrophages and enhanced Schwann cell migration when used as a lumen filler in a rodent model of nerve gap repair using an inert nerve guidance conduit. These results suggest that an injectable PNSECM hydrogel can provide a supportive, bioactive scaffold which promotes repair of peripheral nerve in vivo. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 450-459, 2018.
周围神经在受伤后具有再生和恢复的固有能力。然而,由于修复过程中局部微环境的限制,神经再生通常较为缓慢且不完全。因此,操纵神经修复部位的局部微环境为改善下游结果提供了一个重要机会。巨噬细胞和许旺细胞在外周神经损伤后的早期事件中起着关键作用。我们描述了一种可注射的、周围神经特异性细胞外基质基水凝胶(PNSECM)的制备、表征及其应用,以促进调节鼠坐骨神经损伤模型中神经修复部位的局部巨噬细胞和许旺细胞反应。结果表明,PNSECM 水凝胶在很大程度上保持了与正常天然周围神经组织相关的基质结构。当作为惰性神经引导管用于鼠神经间隙修复模型中的管腔填充物时,PNSECM 水凝胶还被发现可促进巨噬细胞的侵袭,增加 M2 巨噬细胞的比例,并增强许旺细胞的迁移。这些结果表明,可注射的 PNSECM 水凝胶可为体内周围神经修复提供支持性的、生物活性支架。 © 2017 Wiley Periodicals, Inc. J 生物材料 Res 部分 A:106A:450-459,2018 年。