Fabrication and cellular compatibility of aligned chitosan-PCL fibers for nerve tissue regeneration

被引:192
作者
Cooper, Ashleigh [1 ]
Bhattarai, Narayan [1 ]
Zhang, Miqin [1 ]
机构
[1] Univ Washington, Dept Mat Sci & Engn, 302L Roberts Hall, Seattle, WA 98195 USA
关键词
Chitosan; Aligned nanofibers; Tissue engineering; Nerve; NANOFIBROUS SCAFFOLDS; ELECTROSPUN; GROWTH; POLYCAPROLACTONE; ACETYLATION; ALIGNMENT; FTIR;
D O I
10.1016/j.carbpol.2011.02.008
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The ability to produce aligned sub-micron fibers may open new avenues for the development of scaffolds for application in tissue engineering and regenerative medicine. An area of particular interest is functional restoration of damaged or diseased nerves where the aligned fibers serve to support cell adhesion and proliferation, and guide neurite outgrowth in the direction of fiber orientation. In this study, we developed an aligned chitosan-polycaprolactone (chitosan-PCL) fibrous scaffold and investigated how the fiber alignment influenced nerve cell organization and function in comparison with randomly oriented fibrous scaffolds and cast films of the same material. Schwann cells (SCs) were shown to attach and proliferate on all the substrates regardless of their topography, demonstrating the cellular compatibility of the chitosan-PCL material. SCs grown on the aligned chitosan-PCL fibers exhibited a bipolar morphology that oriented along the fiber alignment direction, while those on the films and randomly oriented fibers had a multipolar morphology. Similarly, the chitosan-PCL material supported neuron-like PC-12 cell adhesion, and the aligned fibers regulated the growth of PC-12 cells along the fiber orientation. Additionally, PC-12 cells cultured on the aligned fibers exhibited enhanced unidirectional neurite extension along fiber orientation and significantly higher beta-tubulin gene expression than those grown on chitosan-PCL films and randomly oriented fibers. Our investigation suggested that the aligned chitosan-PCL fibers can serve as a suitable scaffold for improved nerve tissue reconstruction. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:149 / 156
页数:8
相关论文
共 30 条
[11]   Cooperative modulation of neuritogenesis by PC12 cells by topography and nerve growth factor [J].
Foley, JD ;
Grunwald, EW ;
Nealey, PF ;
Murphy, CJ .
BIOMATERIALS, 2005, 26 (17) :3639-3644
[12]   Chitin-based tubes for tissue engineering in the nervous system [J].
Freier, T ;
Montenegro, R ;
Koh, HS ;
Shoichet, MS .
BIOMATERIALS, 2005, 26 (22) :4624-4632
[13]   Electrospun poly(ε-caprolactone)/gelatin nanofibrous scaffolds for nerve tissue engineering [J].
Ghasemi-Mobarakeh, Laleh ;
Prabhakaran, Molamma P. ;
Morshed, Mohammad ;
Nasr-Esfahani, Mohammad-Hossein ;
Ramakrishna, Seeram .
BIOMATERIALS, 2008, 29 (34) :4532-4539
[14]  
GU X, 2010, PROG NEUROBIOL, V93, P204
[15]   In vitro biocompatibility of chitosan-based materials to primary culture of hippocampal neurons [J].
He, Qianru ;
Zhang, Tianyi ;
Yang, Yumin ;
Ding, Fei .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2009, 20 (07) :1457-1466
[16]   Novel chitin and chitosan nanofibers in biomedical applications [J].
Jayakumar, R. ;
Prabaharan, M. ;
Nair, S. V. ;
Tamura, H. .
BIOTECHNOLOGY ADVANCES, 2010, 28 (01) :142-150
[17]   Current applications and future perspectives of artificial nerve conduits [J].
Jiang, Xu ;
Lim, Shawn H. ;
Mao, Hai-Quan ;
Chew, Sing Yian .
EXPERIMENTAL NEUROLOGY, 2010, 223 (01) :86-101
[18]   Chitosan and its derivatives for tissue engineering applications [J].
Kim, In-Yong ;
Seo, Seog-Jin ;
Moon, Hyun-Seuk ;
Yoo, Mi-Kyong ;
Park, In-Young ;
Kim, Bom-Chol ;
Cho, Chong-Su .
BIOTECHNOLOGY ADVANCES, 2008, 26 (01) :1-21
[19]   The Development of Genipin-Crosslinked Poly(caprolactone) (PCL)/Gelatin Nanofibers for Tissue Engineering Applications [J].
Kim, Min Sup ;
Jun, Indong ;
Shin, Young Min ;
Jang, Wonhee ;
Kim, Sun I. ;
Shin, Heungsoo .
MACROMOLECULAR BIOSCIENCE, 2010, 10 (01) :91-100
[20]   Functions of intermediate filaments in neuronal development and disease [J].
Lariviere, RC ;
Julien, JP .
JOURNAL OF NEUROBIOLOGY, 2004, 58 (01) :131-148