A DAMP-scavenging, IL-10-releasing hydrogel promotes neural regeneration and motor function recovery after spinal cord injury

被引:160
作者
Shen, He [1 ]
Xu, Bai [2 ]
Yang, Chao [3 ]
Xue, Weiwei [2 ]
You, Zhifeng [1 ]
Wu, Xianming [2 ]
Ma, Dezun [2 ]
Shao, Dan [3 ]
Leong, Kam [4 ]
Dai, Jianwu [1 ,2 ]
机构
[1] Chinese Acad Sci, Suzhou Inst NanoTech & NanoBion, Div Nanobiomed, Suzhou 215123, Peoples R China
[2] Chinese Acad Sci, Inst Genet & Dev Biol, State Key Lab Mol Dev Biol, Beijing 100101, Peoples R China
[3] South China Univ Technol, Sch Biomed Sci & Engn, Inst Life Sci, Guangzhou Int Campus, Guangzhou 510006, Guangdong, Peoples R China
[4] Columbia Univ, Dept Biomed Engn, New York, NY 10027 USA
基金
中国国家自然科学基金;
关键词
Complete spinal cord injury; Inflammatory microenvironment; Dual-functional scaffold; Hydrogel; Neuroregeneration; TOLL-LIKE RECEPTORS; CELLS; ACTIVATION; DIFFERENTIATION; INTERLEUKIN-10; EXPRESSION; SYSTEM; SCAR;
D O I
10.1016/j.biomaterials.2021.121279
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Spinal cord injury (SCI) creates an inflammatory microenvironment characterized by damage-associated molecular patterns (DAMPs) and immune cell activation that exacerbate secondary damage and impair neurological recovery. Here we develop an immunoregulatory hydrogel scaffold for treating SCI that scavenges DAMPs and slowly releases the anti-inflammatory cytokine interleukin-10 (IL-10). We created this dual-functional scaffold by modifying a photocrosslinked gelatin hydrogel with the cationic, DAMP-binding polymer poly (amidoamine) and with IL-10, and compared the therapeutic activity of this scaffold with that of gelatin-only, gelatin + poly (amidoamine), and gelatin + IL-10 scaffolds in vitro and in vivo. In vitro, the dual-functional scaffold scavenged anionic DAMPs and exhibited sustained release of IL-10, reduced the proinflammatory responses of macrophages and microglia, and enhanced the neurogenic differentiation of neural stem cells. In a complete transection SCI mouse model, the injected dual-functional scaffold suppressed proinflammatory cytokine production, promoted the M2 macrophage/microglia phenotype, and led to neural regeneration and axon growth without scar formation to a greater extent than the single-function or control scaffolds. This DAMP-scavenging, IL-10-releasing scaffold provides a new strategy for promoting neural regeneration and motor function recovery following severe SCI.
引用
收藏
页数:12
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