BD PuraMatrix peptide hydrogel as a culture system for human fetal Schwann cells in spinal cord regeneration

脊髓 脊髓损伤 再生(生物学) 纳米纤维 雪旺细胞 胎儿 自组装肽 坐骨神经 脚手架 病理 医学 化学 解剖 生物医学工程 细胞生物学 生物 材料科学 神经科学 纳米技术 怀孕 遗传学
作者
Fatemeh Moradi,Mehrdad Bahktiari,Mohammad Taghi Joghataei,Maliheh Nobakht,Masoud Soleimani,Gholamreza Hasanzadeh,Ali Fallah,Sam Zarbakhsh,Leila Beigom Hejazian,Maryam Shirmohammadi,Fatemeh Maleki
出处
期刊:Journal of Neuroscience Research [Wiley]
卷期号:90 (12): 2335-2348 被引量:74
标识
DOI:10.1002/jnr.23120
摘要

Abstract BD PuraMatrix peptide hydrogel, a three‐dimensional cell culture model of nanofiber scaffold derived from the self‐assembling peptide RADA16, has been applied to regenerative tissue repair in order to develop novel nanomedicine systems. In this study with PuraMatrix, self‐assembling nanofiber scaffold (SAPNS) and Schwann cells (SCs) were isolated from human fetal sciatic nerves, cultured within SAPNS, and then transplanted into the spinal cord after injury (SCI) in rats. First, the peptide nanofiber scaffold was evaluated via scanning electron microscopy and atomic force microscopy. With phase‐contrast microscopy, the appearance of representative human fetal SCs encapsulated in PuraMatrix on days 3, 5, and 7 in 12‐well plates was revealed. The Schwann cells in PuraMatrix were cultured for 2 days, and the SCs had active proliferative potential. Spinal cord injury was induced by placing a 35‐g weight on the dura of T9–T10 segments for 15 min, followed by in vivo treatment with SAPNS and human fetal SCs (100,000 cells/10 μl/injection) grafted into spinal cord 7 days after SCI. After treatment, the recovery of motor function was assessed periodically using the Basso, Beattie, and Bresnahan scoring system. Eight weeks after grafting, animals were perfusion fixed, and the survival of implanted cells was analyzed with antibody recognizing SCs. Immunohistochemical analysis of grafted lumber segments at 8 weeks after grafting revealed reduced asterogliosis and considerably increased infiltration of endogenous S100 + cells into the injury site, suggesting that PuraMatrix may play an important role in the repair observed after SAPNS and human fetal SC transplantation. © 2012 Wiley Periodicals, Inc.

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