4.8 Article

Peptide-Tethered Hydrogel Scaffold Promotes Recovery from Spinal Cord Transection via Synergism with Mesenchymal Stem Cells

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 9, 期 4, 页码 3330-3342

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b12829

关键词

hyaluronic acid; hydrogel scaffold; mesenchymal stem cells; adhesive peptide; spinal cord injury; tissue engineering

资金

  1. National Natural Science Foundation of China [81102392, 81620108028, 81473143, 81430087]
  2. Natural Science Foundation of Zhejiang Province [LZ14H300001]
  3. Zhejiang Provincial Program for the Cultivation of High -Level Innovative Health Talents
  4. National Science and Technology Major Project [2013ZX09402103]

向作者/读者索取更多资源

Spinal cord injury (SCI) is one of the most devastating injuries. Treatment strategies for SCI are required to overcome comprehensive issues. Implantation of biomaterial scaffolds and stem cells has been demonstrated to be a promising strategy. However, a comprehensive recovery effect is difficult to achieve. In the comprehensive treatment process, the specific roles of the implanted scaffolds and of stem cells in combined strategy are usually neglected. In this study, a peptide modified scaffold is developed based on hyaluronic acid and an adhesive peptide PPFLMLLKGSTR. Synchrotron radiation micro computed tomography measurement provides insights to the three-dimensional inner topographical property and perspective porous structure of the scaffold. The modified scaffold significantly improves cellular survival and adhesive growth of mesenchymal stem cells during 3D culture in vitro. After implantation in transected spinal cord, the modified scaffold and mesenchymal stems are found to function in synergy to restore injured spinal cord tissue, with respective strengths. Hindlimb motor function scores exhibit the most significant impact of the composite implant at 2 weeks post injury, which is the time secondary injury factors begin to take hold. Investigation on the secondary injury factors including inflammatory response and astrocyte overactivity at 10 days post injury reveals the possible underlying reason. Implants of the scaffold, cells, and especially the combination of both elicit inhibitory effects on these adverse factors. The study develops a promising implant for spinal cord tissue engineering and reveals the roles of the scaffold and stem cells. More importantly, the results provide the first understanding of the bioactive peptide PPFLMLLKGSTR concerning its functions on mesenchymal stem cells and spinal cord tissue restoration.

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