脊髓损伤
自愈水凝胶
祖细胞
神经干细胞
脊髓
材料科学
祖细胞
脚手架
生物医学工程
干细胞
细胞生物学
医学
神经科学
生物
高分子化学
作者
Thomas J. Tigner,Gabrielle Dampf,Ashley Tucker,Yu‐Chi Huang,Vipin Jagrit,Abigail J. Clevenger,Arpita Mohapatra,Shreya Raghavan,Jennifer N. Dulin,Daniel L. Alge
标识
DOI:10.1002/adhm.202303912
摘要
Spinal cord injury (SCI) is a serious condition with limited treatment options. Neural progenitor cell (NPC) transplantation is a promising treatment option, and the identification of novel biomaterial scaffolds that support NPC engraftment and therapeutic activity is a top research priority. The objective of this study is to evaluate in situ assembled poly (ethylene glycol) (PEG)-based granular hydrogels for NPC delivery in a murine model of SCI. Microgel precursors are synthesized by using thiol-norbornene click chemistry to react four-armed PEG-amide-norbornene with enzymatically degradable and cell adhesive peptides. Unreacted norbornene groups are utilized for in situ assembly into scaffolds using a PEG-di-tetrazine linker. The granular hydrogel scaffolds exhibit good biocompatibility and do not adversely affect the inflammatory response after SCI. Moreover, when used to deliver NPCs, the granular hydrogel scaffolds supported NPC engraftment, do not adversely affect the immune response to the NPC grafts, and successfully support graft differentiation toward neuronal or astrocytic lineages as well as axonal extension into the host tissue. Collectively, these data establish PEG-based granular hydrogel scaffolds as a suitable biomaterial platform for NPC delivery and justify further testing, particularly in the context of more severe SCI.
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