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Matrix interactions modulate neurotrophin-mediated neurite outgrowth and pathifnding

机译:基质相互作用调节神经营养蛋白介导的神经突向外生长和致病

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Both matrix biochemistry and neurotrophic factors are known to modulate neurite outgrowth and pathifnding; however, the interplay between these two factors is less studied. While previous work has shown that the biochemical identity of the matrix can alter the outgrowth of neurites in response to neurotrophins, the importance of the concentration of cell-adhesive ligands is unknown. Using engineered elastin-like protein matrices, we recently demonstrated a synergistic effect between matrix-bound cell-adhesive ligand density and soluble nerve growth factor treat-ment on neurite outgrowth from dorsal root ganglia. This synergism was mediated by Schwann cell-neurite contact through L1CAM. Cell-adhesive ligand density was also shown to alter the pathifnding behavior of dorsal root ganglion neurites in response to a gradient of nerve growth factor. While more cell-adhesive matrices promoted neurite outgrowth, less cell-adhesive ma-trices promoted more faithful neurite pathifnding. These studies emphasize the importance of considering both matrix biochemistry and neurotrophic factors when designing biomaterials for peripheral nerve regeneration.
机译:已知基质生物化学和神经营养因子均可调节神经突的长出和侵袭。然而,这两个因素之间的相互作用尚待研究。尽管先前的工作表明基质的生化特性可以响应神经营养蛋白改变神经突的生长,但细胞粘附配体浓度的重要性尚不清楚。使用工程化的弹性蛋白样蛋白基质,我们最近证明了基质结合的细胞粘附配体密度和可溶性神经生长因子治疗对背根神经节神经突生长的协同作用。这种协同作用是通过许万氏细胞神经突通过L1CAM接触介导的。还显示细胞粘附的配体密度响应神经生长因子的梯度而改变背根神经节神经突的致病行为。虽然更多的细胞粘附基质促进神经突生长,而更少的细胞粘附基质促进更忠实的神经突寻路。这些研究强调在设计用于周围神经再生的生物材料时,必须同时考虑基质生物化学和神经营养因子。

著录项

  • 来源
    《中国神经再生研究(英文版)》 |2015年第4期|514-517|共4页
  • 作者单位

    Department of Bioengineering, Stanford University, Stanford, CA 94305, USA;

    Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305, USA;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-19 03:44:31
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