神经组织工程中具有排列地形的仿生可注射三维水凝胶

Liza J. Severs, Lindsay N. Cates, Dane M Dewees, Riana T. Hoagland, P. Horner, C. Hofstetter, Zin Z. Khaing
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引用次数: 1

摘要

脊髓损伤导致沿脊柱轴线携带信息的高度组织化细胞结构的破坏。目前,没有临床公认的策略可以帮助脊髓损伤后的轴突再生。实验神经再生的努力包括创造最佳的生物材料与排列的地形,以支持增强的神经元再生。水凝胶是一种高含水量的软质生物材料,被广泛用作与中枢神经系统(CNS)连接的支架。目前可用的方法来创建三维非晶水凝胶内的地形通常是复杂的。在这里,我们研究了一种简单且可重复的方法,该方法使用与神经元细胞兼容的热凝胶仿生聚合物在3D基质中产生一致排列的原纤维。以I型胶原(Col)为基础的热凝胶水凝胶系统与另外两种天然细胞外基质蛋白:层粘连蛋白I (LN)和透明质酸(HA)结合使用。研究了所有凝胶类型(Col、Col LN、Col HA)的凝胶动力学,发现所有三种聚合物组合在37°C下形成一致的凝胶。Col溶液形成凝胶更快(17 min),而Col LN和Col HA需要更长的时间(~22 min)。采用抽吸和喷射的方法制备了含有排列纤维的col基水凝胶。然后用扫描电子显微镜(SEM)检查凝胶。扫描电镜图像证实了所有凝胶类型的成功排列,纤维的大小与胶原蛋白的报道值一致(直径约250 nm)。我们发现胚胎脊髓神经元在体外培养14天后存活并产生与胶原原纤维对齐的过程。接下来,我们研究了在T7/T8胸脊髓挫伤后急性植入对齐和非对齐的Col水凝胶的功能。在所有植入物中均发现泛神经元抗体阳性原纤维,排列的水凝胶支持沿植入水凝胶平行方向的神经突生长。我们的数据表明,热凝胶仿生水凝胶可以通过吸入和喷射的方法产生排列的基质。本文概述的水凝胶的材料组成和排列过程为中枢神经系统的再生治疗提供了一个新的平台,该平台与体外和体内神经元细胞的存活和生长相兼容。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biomimetic Injectable 3D Hydrogels with Aligned Topography for Neural Tissue Engineering
Spinal cord trauma leads to destruction of the highly organized cytoarchitecture that carries information along the axis of the spinal column. Currently, there are no clinically accepted strategies that can help regenerate severed axons after spinal cord injury. Experimental neuroregenerative efforts include the creation of optimal biomaterials with aligned topography to support enhanced neuronal regeneration. Hydrogels are soft biomaterials with high water content that are widely used as scaffolds to interface with the central nervous system (CNS). Current available methods to create topography within the 3D amorphous hydrogels are typically complex. Here we examine a simple and reproducible method that results in consistently aligned fibrils within 3D matrices using thermally gelling biomimetic polymers that are compatible with neuronal cells. A collagen type I (Col)-based thermally gelling hydrogel system was used in combination with two other native extracellular matrix proteins: laminin I (LN), and hyaluronic acid (HA). Gelling kinetics for all gel types (Col, Col LN, Col HA) were examined, and we found that all three combinations of polymer formed consistent gels at 37°C. Col solution was faster to form gels (17 min), while Col LN and Col HA took longer (~22 minutes). A method of aspiration and ejection was used to produce Col-based hydrogels containing aligned fibrils. Gels were then examined using scanning electron microscopy (SEM). SEM images confirmed successful alignment in all gel types, and the size of fibers was consistent with reported values for collagen (~250 nm in diameter). We found that embryonic spinal cord neurons survive and produce processes aligned to collagen fibrils after 14 days in vitro. Next, we investigated the functionality of aligned and non-aligned Col hydrogels implanted acutely after a contusion type spinal cord injury to the thoracic spinal cord at T7/T8. Pan neuronal antibody-positive fibrils were found within all implants, aligned hydrogels supported neurite growth along the parallel direction of the implanted hydrogels. Our data indicate that thermally gelling biomimetic hydrogels can produce aligned matrices by a method of aspiration and ejection. The material composition and process of aligning hydrogels outlined here presents a novel platform for regenerative therapies for the CNS that is compatible with the survival and growth of neuronal cells in vitro and in vivo.
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