Neural cell type-specific responses to glycomimetic functionalized collagen

被引:26
|
作者
Masand, Shirley N. [1 ]
Perron, Isaac J. [1 ]
Schachner, Melitta [2 ,3 ]
Shreiber, David I. [1 ]
机构
[1] Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, WM Keck Ctr Collaborat Neurosci, Piscataway, NJ 08854 USA
[3] Rutgers State Univ, Dept Cell Biol & Neurosci, Piscataway, NJ 08854 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Nerve regeneration; PSA; HNK-1; Glycans; PERIPHERAL-NERVE REGENERATION; POLYSIALIC ACID; SCHWANN-CELLS; L2/HNK-1; CARBOHYDRATE; NEURITE OUTGROWTH; ADHESION MOLECULE; MOTOR-NEURONS; GROWTH-FACTOR; RGD PEPTIDES; RECOVERY;
D O I
10.1016/j.biomaterials.2011.10.013
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Despite their noted functional role, glycans have had limited therapeutic use due to difficulties in synthesis and quick degradation in vivo. The recent discovery of glycomimetics has provided new opportunities for their application. In this study, we have functionalized type I collagen with peptide mimics of two glycans: (1) polysialic acid (PSA) and (2) an epitope first discovered on human natural killer cells (HNK-1). These glycans and their glycomimetic counterparts have been shown to be important regulators of repair following injury through their unique and phenotypically specific effects on neural behavior. We show that these molecules retain their bioactivity following functionalization to the collagen backbone. Grafted HNK-1 encouraged motor neuron outgrowth, while grafted PSA encouraged sensory and motor neuron outgrowth and enhanced Schwann cell proliferation and process extension. These data support the potential of glycomimetic-functionalized collagen as a biomaterial strategy to increase the efficiency of synaptic reconnection following nervous system injury. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:790 / 797
页数:8
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