Poly-L-ornithine enhances migration of neural stem/progenitor cells via promoting α-Actinin 4 binding to actin filaments

被引:32
作者
Ge, Hongfei [1 ,2 ]
Yu, Anyong [3 ]
Chen, Jingyu [1 ,2 ]
Yuan, Jichao [1 ,2 ]
Yin, Yi [1 ,2 ]
Duanmu, Wangsheng [1 ,2 ]
Tan, Liang [1 ,2 ]
Yang, Yang [1 ,2 ]
Lan, Chuan [1 ,2 ]
Chen, Weixiang [1 ,2 ]
Feng, Hua [1 ,2 ]
Hu, Rong [1 ,2 ]
机构
[1] Third Mil Med Univ, Southwest Hosp, Dept Neurosurg, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Southwest Hosp, Key Lab Neurotrauma, Chongqing 400038, Peoples R China
[3] Zunyi Med Coll, Affiliated Hosp 1, Dept Emergency, Zunyi 563003, Guizhou, Peoples R China
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
中国国家自然科学基金;
关键词
EPIDERMAL-GROWTH-FACTOR; STEM-CELLS; ALGINATE MICROCAPSULES; SELECTIVE EXPANSION; PROGENITOR CELLS; DIFFERENTIATION; FILOPODIA; ADHESION; BRAIN; NEUROGENESIS;
D O I
10.1038/srep37681
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The recruitment of neural stem/progenitor cells (NSPCs) for brain restoration after injury is a promising regenerative therapeutic strategy. This strategy involves enhancing proliferation, migration and neuronal differentation of NSPCs. To date, the lack of biomaterials, which facilitate these processes to enhance neural regeneration, is an obstacle for the cell replacement therapies. Our previous study has shown that NSPCs grown on poly-L-ornithine (PO) could proliferate more vigorously and differentiate into more neurons than that on Poly-L-Lysine (PLL) and Fibronectin (FN). Here, we demonstrate that PO could promote migration of NSPCs in vitro, and the underlying mechanism is PO activates alpha-Actinins 4 (ACTN4), which is firstly certified to be expessed in NSPCs, to promote filopodia formation and therefore enhances NSPCs migration. Taken together, PO might serve as a better candidate for transplanted biomaterials in the regenerative therapeutic strategy, compared with PLL and FN.
引用
收藏
页数:11
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