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首页> 外文期刊>Journal of nanomaterials >Self-assembling peptide nanofiber scaffold enhanced with RhoA inhibitor CT04 improves axonal regrowth in the transected spinal cord
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Self-assembling peptide nanofiber scaffold enhanced with RhoA inhibitor CT04 improves axonal regrowth in the transected spinal cord

机译:RhoA抑制剂CT04增强的自组装肽纳米纤维支架可改善横断脊髓的轴突再生长

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摘要

The present study was designed to explore the therapeutic potential of self-assembling peptide nanofiber scaffold (SAPNS) delivered RhoA inhibitor to ameliorate the hostile microenvironment of injured spinal cord for axonal regeneration. After a transection was applied to the thoracic spinal cord of mice, the combination of SAPNS and CT04 (a cell permeable RhoA inhibitor), single SAPNS with vehicle, or saline was transplanted into the lesion cavity. Results showed that SAPNS+CT04 implants achieved the best therapeutic outcomes among treatment groups. The novel combination not only reconstructed the injured nerve gap but also elicited significant axonal regeneration and motor functional recovery. Additionally, the combination also effectively reduced the apoptosis and infiltration of activated macrophages in the injured spinal cord. Collectively, the present study demonstrated that SAPNS-based delivery of RhoA inhibitor CT04 presented a highly potential therapeutic strategy for spinal cord injury with reknitting lesion gap, attenuating secondary injury, and improving axonal regrowth.
机译:本研究旨在探讨自组装肽纳米纤维支架(SAPNS)递送的RhoA抑制剂改善受损脊髓轴突再生的不利微环境的治疗潜力。在将横切线应用于小鼠的胸脊髓后,将SAPNS和CT04(细胞可渗透的RhoA抑制剂),具有载体的单SAPNS或盐水的组合移植到病变腔中。结果表明,SAPNS + CT04植入物在治疗组中获得了最佳的治疗效果。这种新颖的组合不仅可以重建受损的神经间隙,还可以引起明显的轴突再生和运动功能恢复。另外,该组合还有效减少了受损脊髓中凋亡和活化巨噬细胞的浸润。总体而言,本研究表明,基于SAPNS的RhoA抑制剂CT04的递送为脊髓损伤提供了高度潜在的治疗策略,可重新编织病灶间隙,减轻继发性损伤并改善轴突再生长。

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