Three-Dimensional Nanofibrous Scaffolds Incorporating Immobilized BDNF Promote Proliferation and Differentiation of Cortical Neural Stem Cells

被引:131
作者
Horne, Malcolm K. [2 ]
Nisbet, David R. [3 ,4 ]
Forsythe, John S. [3 ]
Parish, Clare L. [1 ]
机构
[1] Univ Melbourne, Florey Neurosci Inst, Ctr Neurosci, Melbourne, Vic 3010, Australia
[2] St Vincents Hosp, Fitzroy, Vic 3065, Australia
[3] Monash Univ, Dept Mat Engn, Div Biol Engn, Melbourne, Vic 3004, Australia
[4] Mental Hlth Res Inst Victoria, Parkville, Vic, Australia
基金
澳大利亚国家健康与医学研究理事会; 澳大利亚研究理事会;
关键词
EPIDERMAL-GROWTH-FACTOR; GUIDE NEURITE OUTGROWTH; SPINAL-CORD-INJURY; CONCENTRATION GRADIENTS; ELECTROSPUN NANOFIBERS; CORTICOSPINAL NEURONS; EXTRACELLULAR-MATRIX; HYDROGEL SCAFFOLDS; DEPENDENT SURVIVAL; FIBERS;
D O I
10.1089/scd.2009.0158
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Attempts to repair the central nervous system damaged as a result of trauma or disease will depend on the ability to restore the appropriate neuronal connectivity. This will rely on establishing appropriate chemical and physical environments for supporting neural cells and their processes and in this regard, engineering of biomaterials is of increasing interest. It will be important to understand how cells behave on these biomaterials in vitro, prior to future in vivo application. We reveal that modification of 3-dimensional (3D) electrospun poly-e-caprolactone (PCL) nanofiber scaffolds by fiber alignment and aminolysation is superior to classical 2-dimensional (2D) culture-ware in promoting in vitro proliferation and differentiation of cortical cells. Many studies have examined the importance of exogenous soluble factors to promote cell fate specification. Here, we demonstrate that tethering the neurotrophin, brain-derived neurotrophic factor (BDNF), onto modified nanofibers is superior to culturing in the presence of soluble BDNF. Functional immobilization of BDNF to polymer nanofibers enhances neural stem cell (NSC) proliferation and directs cell fate toward neuronal and oligodendrocyte specification, essential for neural tissue repair. These findings indicate that modified PCL nanofibrous 3D scaffolds are capable of supporting NSCs and their derivatives and may present a new avenue for encouraging neural repair in the future.
引用
收藏
页码:843 / 852
页数:10
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