Three-dimensional nanofibrillar surfaces covalently modified with tenascin-C-derived peptides enhance neuronal growth in vitro

被引:75
作者
Ahmed, I
Liu, HY
Mamiya, PC
Ponery, AS
Babu, AN
Weik, T
Schindler, M
Meiners, S
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Pharmacol, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Dept Psychol, New Brunswick, NJ 08903 USA
[3] Donaldson Co Inc, Minneapolis, MN 55440 USA
[4] Michigan State Univ, Dept Biochem & Mol Biol, E Lansing, MI 48824 USA
关键词
nanofiber; neuron; tenascin-C; peptide; extracellular matrix;
D O I
10.1002/jbm.a.30587
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Current methods to promote growth Of Cultured neurons use two-dimensional (2D) glass or polystyrene Surfaces coated with a charged molecule (e.g. poly-L-lysine (PLL)) or an isolated extracellular matrix (ECM) protein (e.g. laminin-1.). However, these 2D Surfaces represent a poor topological approximation of the three-dimensional (3D) architecture of the assembled ECM that regulates neuronal growth ill vivo. Here we report on the development of a new 3D synthetic nanofibrillar surface for the culture of neurons. This nanofibrillar surface is composed of polyamide nanofibers whose organization mimics the porosity and geometry of the ECM. Neuronal adhesion and neurite outgrowth from cerebellar granule, cerebral cortical, hippocampal, motor, and dorsal root ganglion neurons were similar on nanofibers and PLL-coated glass coverslips; however, neurite generation was increased, Moreover, covalent modification of the nanofibers with neuroactive peptides derived from human teriascin-C significantly enhanced the ability of the nanofibers to facilitate neuronal attachment, neurite generation, and neurite extension in vitro. Hence the 3D nanofibrillar surface provides a physically and chemically stabile cell Culture surface for neurons and, potentially, an exciting new opportunity for the development of peptide-modified matrices for use in strategies designed to encourage axonal regrowth following central nervous system injury. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:851 / 860
页数:10
相关论文
共 38 条
[1]  
Abramoff MD., 2004, Biophot. Int., V11, P36, DOI DOI 10.1201/9781420005615.AX4
[2]  
Abrams GA, 2000, CELL TISSUE RES, V299, P39, DOI 10.1007/s004410050004
[3]  
AKBUM BF, 2004, NAT NEUROSCI, V7, P145
[4]  
Chernousov MA, 2000, HISTOL HISTOPATHOL, V15, P593, DOI 10.14670/HH-15.593
[5]   Poly(L-lysine) as a model drug macromolecule with which to investigate secondary structure and membrane transport, part I: physicochemical and stability studies [J].
Chittchang, M ;
Alur, HH ;
Mitra, AK ;
Johnston, TP .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2002, 54 (03) :315-323
[6]  
Chung HY, 2004, Polymer, polymer microfiber, polymer nanofiber and applications including filter structures. US Patent No, Patent No. [6,743,273 B2, 6743273]
[7]   Taking cell-matrix adhesions to the third dimension [J].
Cukierman, E ;
Pankov, R ;
Stevens, DR ;
Yamada, KM .
SCIENCE, 2001, 294 (5547) :1708-1712
[8]   Decorin suppresses neurocan, brevican, phosphacan and NG2 expression and promotes axon growth across adult rat spinal cord injuries [J].
Davies, JE ;
Tang, XF ;
Denning, JW ;
Archibald, SJ ;
Davies, SJA .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2004, 19 (05) :1226-1242
[9]   A cultural renaissance: in vitro cell biology embraces three-dimensional context [J].
Edelman, DB ;
Keefer, EW .
EXPERIMENTAL NEUROLOGY, 2005, 192 (01) :1-6
[10]  
ESCURAT M, 1990, J NEUROSCI, V10, P764