Shang Junkui, Qiao Hui, Hao Peng, Gao Yudan, Zhao Wen, Duan Hongmei, Yang Zhaoyang, Li Xiaoguang
J Biomed Nanotechnol. 2019 Apr 1;15(4):703-716. doi: 10.1166/jbn.2019.2732.
Neural circuit reconstruction is the main target of functional restoration after adult spinal cord injury (SCI). The microenvironment after adult SCI is hostile to neural regeneration. Here, we designed a bFGF controlled releasing system (bFGF-CRS) by loading bFGF onto the sodium hyaluronate collagen scaffolds to modify the hostile microenvironment. We found that the bFGF-CRS scaffolds had proper mechanical properties for spinal cord regeneration and could slowly release bFGF for up to 6 weeks under the physiological condition. After implantation, the bFGF-CRS scaffolds could reduce microglial activation, promote revascularization, elicit endogenous neurogenesis and promote regrowth of transected axons. The endogenous mature newly born neurons could form synaptic-like connections with each other or with host neurons, including cortex neurons, brainstem neurons and spinal interneurons. The functional nascent neural networks between the lesion area and the host spinal cord were established. It eventually led to hindlimb locomotion recovery. Our study suggests that the bFGF-CRS scaffolds, modifying the microenvironment of the lesion area, can rebuild the damaged neural circuit, thus support great potential for SCI treatment in the clinical application.
神经回路重建是成年脊髓损伤(SCI)后功能恢复的主要目标。成年SCI后的微环境不利于神经再生。在此,我们通过将碱性成纤维细胞生长因子(bFGF)负载到透明质酸钠胶原蛋白支架上,设计了一种bFGF控释系统(bFGF-CRS),以改善这种不利的微环境。我们发现,bFGF-CRS支架具有适合脊髓再生的机械性能,并且在生理条件下能够缓慢释放bFGF长达6周。植入后,bFGF-CRS支架可以减少小胶质细胞的激活,促进血管再生,引发内源性神经发生,并促进横断轴突的再生。内源性成熟的新生神经元可以相互之间或与宿主神经元(包括皮层神经元、脑干神经元和脊髓中间神经元)形成类似突触的连接。在损伤区域和宿主脊髓之间建立了功能性的新生神经网络。最终导致后肢运动功能恢复。我们的研究表明,bFGF-CRS支架通过改善损伤区域的微环境,可以重建受损的神经回路,因此在临床应用中为SCI治疗提供了巨大的潜力。