Panzer Kate V, Burrell Justin C, Helm Kaila V T, Purvis Erin M, Zhang Qunzhou, Le Anh D, O'Donnell John C, Cullen D Kacy
Center for Brain Injury and Repair, Department of Neurosurgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Center for Neurotrauma, Neurodegeneration and Restoration, Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA, United States.
Front Bioeng Biotechnol. 2020 Nov 20;8:580654. doi: 10.3389/fbioe.2020.580654. eCollection 2020.
Following peripheral nerve injury comprising a segmental defect, the extent of axon regeneration decreases precipitously with increasing gap length. Schwann cells play a key role in driving axon re-growth by forming aligned tubular guidance structures called bands of Büngner, which readily occurs in distal nerve segments as well as within autografts - currently the most reliable clinically-available bridging strategy. However, host Schwann cells generally fail to infiltrate large-gap acellular scaffolds, resulting in markedly inferior outcomes and motivating the development of next-generation bridging strategies capable of fully exploiting the inherent pro-regenerative capability of Schwann cells. We sought to create preformed, implantable Schwann cell-laden microtissue that emulates the anisotropic structure and function of naturally-occurring bands of Büngner. Accordingly, we developed a biofabrication scheme leveraging biomaterial-induced self-assembly of dissociated rat primary Schwann cells into dense, fiber-like three-dimensional bundles of Schwann cells and extracellular matrix within hydrogel micro-columns. This engineered microtissue was found to be biomimetic of morphological and phenotypic features of endogenous bands of Büngner, and also demonstrated 8 and 2× faster rates of axonal extension from primary rat spinal motor neurons and dorsal root ganglion sensory neurons, respectively, compared to 3D matrix-only controls or planar Schwann cells. To our knowledge, this is the first report of accelerated motor axon outgrowth using aligned Schwann cell constructs. For translational considerations, this microtissue was also fabricated using human gingiva-derived Schwann cells as an easily accessible autologous cell source. These results demonstrate the first tissue engineered bands of Büngner (TE-BoBs) comprised of dense three-dimensional bundles of longitudinally aligned Schwann cells that are readily scalable as implantable grafts to accelerate axon regeneration across long segmental nerve defects.
在包括节段性缺损的周围神经损伤后,随着间隙长度的增加,轴突再生的程度会急剧下降。雪旺细胞通过形成称为Büngner带的排列成管状的引导结构,在驱动轴突重新生长中起关键作用,这在远端神经节段以及自体移植物中很容易发生,自体移植物是目前临床上最可靠的桥接策略。然而,宿主雪旺细胞通常无法浸润大间隙无细胞支架,导致结果明显较差,这促使人们开发能够充分利用雪旺细胞固有促再生能力的下一代桥接策略。我们试图创建预先形成的、可植入的载有雪旺细胞的微组织,以模拟天然Büngner带的各向异性结构和功能。因此,我们开发了一种生物制造方案,利用生物材料诱导解离的大鼠原代雪旺细胞自组装成水凝胶微柱内致密的、纤维状的三维雪旺细胞和细胞外基质束。研究发现,这种工程化微组织模仿了内源性Büngner带的形态和表型特征,并且与仅含三维基质的对照或平面雪旺细胞相比,分别显示出大鼠原代脊髓运动神经元和背根神经节感觉神经元的轴突延伸速度快8倍和2倍。据我们所知,这是使用排列的雪旺细胞构建体加速运动轴突生长的首次报道。出于转化研究的考虑,这种微组织也使用人牙龈来源的雪旺细胞作为易于获取的自体细胞来源制造。这些结果证明了首个由纵向排列的雪旺细胞致密三维束组成的组织工程化Büngner带(TE-BoBs),它可以很容易地扩展为可植入移植物,以加速跨长节段神经缺损的轴突再生。