Barberat Sacha, Nagarajan Sakthivel, Habib Michel, Lebrun Aurélien, Nieswic Naomi, Lauzon Marc-Antoine, Aubert-Pouëssel Anne, Blanquer Sébastien, Labour Marie-Noëlle
ICGM, Univ Montpellier, CNRS, ENSCM, 34293 Montpellier, France.
PAC Chimie Balard, Univ Montpellier, CNRS, ENSCM, 34293 Montpellier, France.
ACS Biomater Sci Eng. 2025 Sep 8;11(9):5498-5511. doi: 10.1021/acsbiomaterials.5c00479. Epub 2025 Aug 18.
Peripheral nerve injury increasingly affects people around the world, leading to very incapacitating conditions with the loss of motor and sensory functions. Combining biomaterials with glial cells is particularly promising to reconnect injured axons to their original target, as they represent a supportive environment facilitating cell and axonal growth. Neural tissue engineering using biomimetic soft scaffolds often faces challenges related to handling, suturability, and integration into the host tissue. This study aimed to develop a soft and flexible biomimetic scaffold that supports colonization with a high density of glial Schwann cells (SCs). The strategy consists of printing tubular multichannel (500 to 1000 μm channels) nerve guides (NG) (5 × 5 mm) presenting an anisotropic architecture using a high-resolution stereolithography printing process. To this aim, the synthesis of photosensitive methacrylated gelatin (GelMA) inks was optimized and combined with various ratios of dimethacrylated F127 Pluronic. We showed that the physicochemical and mechanical properties of the printed hydrogels can be controlled by polymer concentrations and ratios. Specifically, in a 12:3 GelMA:F127DMA ratio, Pluronic provides enhanced flexibility while maintaining softness similar to nerve tissues. Importantly, gelatin-Pluronic scaffolds better withstand handling than gelatin scaffolds, as demonstrated by a higher strain at break in compression assays. Moreover, strain at break in suturing experiments was more than doubled with GelMA:F127DMA (35%) hydrogels in contrast to fragile and brittle gelatin-only scaffolds (15%). Schwann cells adhere, proliferate, and remain viable over 7 days within the channels demonstrating that these cellularized gelatin-Pluronic nerve guides hold significant promise for nerve regeneration.
周围神经损伤在全球范围内对人们的影响日益增加,会导致运动和感觉功能丧失,造成严重的功能障碍。将生物材料与神经胶质细胞相结合对于使受损轴突重新连接到其原始靶点特别有前景,因为它们代表了一个有利于细胞和轴突生长的支持性环境。使用仿生软支架的神经组织工程常常面临与操作、可缝合性以及与宿主组织整合相关的挑战。本研究旨在开发一种柔软且灵活的仿生支架,以支持高密度的施万细胞(SCs)定植。该策略包括使用高分辨率立体光刻印刷工艺打印具有各向异性结构的管状多通道(通道直径为500至1000μm)神经导管(NG)(尺寸为5×5mm)。为此,对光敏甲基丙烯酸化明胶(GelMA)油墨的合成进行了优化,并与不同比例的二甲基丙烯酸化F127普朗尼克相结合。我们表明,打印水凝胶的物理化学和机械性能可通过聚合物浓度和比例来控制。具体而言,在GelMA:F127DMA比例为12:3时,普朗尼克在保持与神经组织相似柔软度的同时增强了柔韧性。重要的是,明胶 - 普朗尼克支架在处理时比明胶支架更耐用,这在压缩试验中表现为更高的断裂应变。此外,与易碎且脆的仅含明胶的支架(15%)相比,GelMA:F127DMA(35%)水凝胶在缝合实验中的断裂应变增加了一倍多。施万细胞在通道内7天内能够黏附、增殖并保持存活,这表明这些细胞化的明胶 - 普朗尼克神经导管在神经再生方面具有巨大潜力。