State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou 510060, China.
PCFM Lab, GD HPPC Lab, School of Chemistry, Sun Yat-sen University, Guangzhou 510275, China.
ACS Appl Bio Mater. 2021 Aug 16;4(8):6473-6487. doi: 10.1021/acsabm.1c00616. Epub 2021 Aug 5.
Decellularized peripheral nerve matrix hydrogel (DNM-G) has drawn increasing attention in the field of neural tissue engineering, owing to its high tissue-specific bioactivity, drug/cell delivery capability, and multifunctional processability. However, the mechanisms and influencing factors of DNM-G formation have been rarely reported. To enable potential biological applications, the relationship between gelation conditions (including digestion time and gel concentration) and mechanical properties/stability (sol-gel transition temperature, gelation time, nanotopology, and storage modulus) of the DNM-G were systematically investigated in this study. The adequate-digested decellularized nerve matrix solution exhibited higher mechanical property, shorter gelation time, and a lower gelation temperature. A noteworthy increase of β-sheet proportion was identified through Fourier-transform infrared spectroscopy (FTIR) and circular dichroism (CD) characterizations, which suggested the possible major secondary structure formation during the phase transition. Besides, the DNM-G degraded fast that over 70% mass loss was noted after 4 weeks when immersing in PBS. A natural cross-linking agent, genipin, was gently introduced into DNM-G to enhance its mechanical properties and stability without changing its microstructure and biological performance. As a prefabricated scaffold, DNM-G remarkably increased the length and penetration depth of dorsal root ganglion (DRG) neurites compared to collagen gel. Furthermore, the DNM-G promoted the myelination and facilitated the formation of the morphological neural network. Finally, we demonstrated the feasibility of applying DNM-G in support-free extrusion-based 3D printing. Overall, the mechanical and biological performance of DNM-G can be manipulated by tuning the processing parameters, which is key to the versatile applications of DNM-G in regenerative medicine.
去细胞周围神经基质水凝胶(DNM-G)由于其具有高组织特异性生物活性、药物/细胞递送能力和多功能加工性能,在神经组织工程领域引起了越来越多的关注。然而,DNM-G 形成的机制和影响因素很少有报道。为了实现潜在的生物学应用,本研究系统研究了凝胶化条件(包括消化时间和凝胶浓度)与 DNM-G 的机械性能/稳定性(溶胶-凝胶转变温度、凝胶化时间、纳米拓扑结构和储能模量)之间的关系。充分消化的去细胞神经基质溶液表现出更高的机械性能、更短的凝胶化时间和更低的凝胶化温度。傅里叶变换红外光谱(FTIR)和圆二色性(CD)特性表明,β-折叠比例显著增加,这表明在相变过程中可能形成主要的二级结构。此外,DNM-G 降解迅速,在 PBS 中浸泡 4 周后,超过 70%的质量损失。一种天然交联剂京尼平被温和地引入 DNM-G 中,以增强其机械性能和稳定性,而不会改变其微观结构和生物性能。作为预制支架,与胶原凝胶相比,DNM-G 显著增加了背根神经节(DRG)神经突的长度和穿透深度。此外,DNM-G 促进了髓鞘形成并有助于形态神经网络的形成。最后,我们证明了在无支撑挤出式 3D 打印中应用 DNM-G 的可行性。总之,通过调整加工参数可以控制 DNM-G 的机械和生物学性能,这是 DNM-G 在再生医学中多功能应用的关键。