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富含 GDNF 的去细胞细胞外基质增强神经发生和髓鞘再生,促进脊髓损伤后的运动功能恢复。

Decellularized extracellular matrix enriched with GDNF enhances neurogenesis and remyelination for improved motor recovery after spinal cord injury.

机构信息

Key Laboratory for Ultrafine Materials of Ministry of Education, Frontiers Science Center for Materiobiology and Dynamic Chemistry, Engineering Research Center for Biomaterials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, PR China.

Key Laboratory for Ultrafine Materials of Ministry of Education, Frontiers Science Center for Materiobiology and Dynamic Chemistry, Engineering Research Center for Biomaterials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, PR China.

出版信息

Acta Biomater. 2024 May;180:308-322. doi: 10.1016/j.actbio.2024.04.015. Epub 2024 Apr 16.

Abstract

Motor functional improvement represents a paramount treatment objective in the post-spinal cord injury (SCI) recovery process. However, neuronal cell death and axonal degeneration following SCI disrupt neural signaling, impeding the motor functional recovery. In this study, we developed a multifunctional decellularized spinal cord-derived extracellular matrix (dSECM), crosslinked with glial cell-derived neurotrophic factor (GDNF), to promote differentiation of stem cells into neural-like cells and facilitate axonogenesis and remyelination. After decellularization, the immunogenic cellular components were effectively removed in dSECM, while the crucial protein components were retained which supports stem cells proliferation and differentiation. Furthermore, sustained release of GDNF from the dSECM facilitated axonogenesis and remyelination by activating the PI3K/Akt and MEK/Erk pathways. Our findings demonstrate that the dSECM-GDNF platform promotes neurogenesis, axonogenesis, and remyelination to enhance neural signaling, thereby yielding promising therapeutic effects for motor functional improvement after SCI. STATEMENT OF SIGNIFICANCE: The dSECM promotes the proliferation and differentiation of MSCs or NSCs by retaining proteins associated with positive regulation of neurogenesis and neuronal differentiation, while eliminating proteins related to negative regulation of neurogenesis. After crosslinking, GDNF can be gradually released from the platform, thereby promoting neural differentiation, axonogenesis, and remyelination to enhance neural signaling through activation of the PI3K/Akt and MEK/Erk pathways. In vivo experiments demonstrated that dSECM-GDNF/MSC@GelMA hydrogel exhibited the ability to facilitate neuronal regeneration at 4 weeks post-surgery, while promoting axonogenesis and remyelination at 8 weeks post-surgery, ultimately leading to enhanced motor functional recovery. This study elucidates the ability of neural regeneration strategy to promote motor functional recovery and provides a promising approach for designing multifunctional tissue for SCI treatment.

摘要

运动功能的改善是脊髓损伤(SCI)后康复过程中的首要治疗目标。然而,SCI 后神经元细胞死亡和轴突变性会破坏神经信号传递,阻碍运动功能的恢复。在这项研究中,我们开发了一种多功能去细胞化脊髓源性细胞外基质(dSECM),与胶质细胞源性神经营养因子(GDNF)交联,以促进干细胞向神经样细胞分化,并促进轴突发生和髓鞘再生。去细胞化后,dSECM 中有效的去除了免疫原性细胞成分,同时保留了支持干细胞增殖和分化的关键蛋白成分。此外,dSECM 中 GDNF 的持续释放通过激活 PI3K/Akt 和 MEK/Erk 通路促进了轴突发生和髓鞘再生。我们的研究结果表明,dSECM-GDNF 平台通过促进神经发生、轴突发生和髓鞘再生来增强神经信号传递,从而为 SCI 后运动功能改善提供了有前景的治疗效果。

意义声明

dSECM 通过保留与神经发生和神经元分化的正调控相关的蛋白,同时消除与神经发生的负调控相关的蛋白,促进 MSC 或 NSC 的增殖和分化。交联后,GDNF 可以从平台上逐渐释放,从而通过激活 PI3K/Akt 和 MEK/Erk 通路促进神经分化、轴突发生和髓鞘再生,增强神经信号传递。体内实验表明,dSECM-GDNF/MSC@GelMA 水凝胶在手术后 4 周表现出促进神经元再生的能力,而在手术后 8 周表现出促进轴突发生和髓鞘再生的能力,最终导致运动功能恢复增强。本研究阐明了神经再生策略促进运动功能恢复的能力,并为设计用于 SCI 治疗的多功能组织提供了一种有前途的方法。

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