Chitosan Degradation Products Promote Nerve Regeneration by Stimulating Schwann Cell Proliferation via miR-27a/FOXO1 Axis

被引:79
|
作者
Wang, Yongjun [1 ,2 ]
Zhao, Yahong [1 ,2 ]
Sun, Cheng [1 ,2 ]
Hu, Wen [1 ,2 ]
Zhao, Jing [1 ,2 ]
Li, Guicai [1 ,2 ]
Zhang, Luzhong [1 ,2 ]
Liu, Mei [1 ,2 ]
Liu, Yan [1 ,2 ]
Ding, Fei [1 ,2 ]
Yang, Yumin [1 ,2 ]
Gu, Xiaosong [1 ,2 ]
机构
[1] Nantong Univ, Key Lab Neuroregenerat, Nantong 226001, Peoples R China
[2] Coinnovat Ctr Neuroregenerat, Nantong 226001, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomaterials; Polysaccharides; miRNA; Oligosaccharides; Regeneration; BREAST-CANCER CELLS; PERIPHERAL-NERVE; FORKHEAD TRANSCRIPTION; EARLY-STAGE; IN-VITRO; EXPRESSION; FOXO1; CHITOOLIGOSACCHARIDE; OLIGOSACCHARIDES; MIR-27;
D O I
10.1007/s12035-014-8968-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Natural polysaccharides are biomaterials widely used for constructing scaffolds in tissue engineering. While natural polysaccharides have been shown to robustly promote tissue regeneration, the underlying molecular mechanism remains largely unknown. Here, we show that chitooligosaccharides (COS), the intermediate products of chitosan degradation, stimulate peripheral nerve regeneration in rats. Our experiment also shows that COS stimulate the proliferation of Schwann cells (SCs) during nerve regeneration. By analyzing the transcriptome and gene regulatory network, we identified the miR-27a/FOXO1 axis as the main signaling pathway for mediating the proliferative effects of COS on SCs. COS increase the expression level of miR-27a and cause a reduction of FOXO1, which subsequently accelerates the cell cycle and stimulates SC proliferation to stimulate nerve regeneration. These findings define a basic pathway for oligosaccharides-mediated cell proliferation and reveal a novel aspect of polysaccharide biomaterials in tissue engineering.
引用
收藏
页码:28 / 39
页数:12
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