硫酸软骨素生物材料亲和递送NGF的研究进展。

Biomatter Pub Date : 2011-10-01 DOI:10.4161/biom.18791
Karen Chao Butterfield, Aaron W Conovaloff, Alyssa Panitch
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引用次数: 25

摘要

硫酸软骨素是中枢和周围神经系统细胞外基质的主要成分。硫酸软骨素在损伤时上调,因此需要通过富含硫酸软骨素的基质和合成支架促进神经突延伸的方法。我们描述了使用硫酸软骨素和一种新的硫酸软骨素结合肽来控制神经生长因子的释放。有趣的是,新型硫酸软骨素结合肽增强了硫酸软骨素凝胶的控释特性。在支架中引入硫酸软骨素可抑制皮层的初生生长,而硫酸软骨素、硫酸软骨素结合肽和神经生长因子的结合可促进硫酸软骨素凝胶中皮层神经突的初生生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial.

Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial.

Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial.

Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial.

Chondroitin sulfate is a major component of the extracellular matrix in both the central and peripheral nervous systems. Chondroitin sulfate is upregulated at injury, thus methods to promote neurite extension through chondroitin sulfate-rich matrices and synthetic scaffolds are needed. We describe the use of both chondroitin sulfate and a novel chondroitin sulfate-binding peptide to control the release of nerve growth factor. Interestingly, the novel chondroitin sulfate-binding peptide enhances the controlled release properties of the chondroitin sulfate gels. While introduction of chondroitin sulfate into a scaffold inhibits primary cortical outgrowth, the combination of chondroitin sulfate, chondroitin sulfate-binding peptide and nerve growth factor promotes primary cortical neurite outgrowth in chondroitin sulfate gels.

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