Topographically modified surfaces affect orientation and growth of hippocampal neurons

被引:175
作者
Dowell-Mesfin, N. M. [1 ,2 ]
Abdul-Karim, M-A [3 ]
Turner, A. M. P. [4 ]
Schanz, S. [2 ]
Craighead, H. G. [4 ]
Roysam, B. [3 ]
Turner, J. N. [1 ,2 ]
Shain, W. [1 ,2 ]
机构
[1] SUNY Albany, Sch Publ Hlth, Albany, NY USA
[2] Wadsworth Ctr, Albany, NY 12201 USA
[3] Rensselaer Polytech Inst, Troy, NY 12180 USA
[4] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14853 USA
关键词
D O I
10.1088/1741-2560/1/2/003
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Extracellular matrix molecules provide biochemical and topographical cues that influence cell growth in vivo and in vitro. Effects of topographical cues on hippocampal neuron growth were examined after 14 days in vitro. Neurons from hippocampi of rat embryos were grown on poly-L-lysine-coated silicon surfaces containing fields of pillars with varying geometries. Photolithography was used to fabricate 1 mu m high pillar arrays with different widths and spacings. beta(III)-tubulin and MAP-2 immunocytochemistry and scanning electron microscopy were used to describe neuronal processes. Automated two-dimensional tracing software quantified process orientation and length. Process growth on smooth surfaces was random, while growth on pillared surfaces exhibited the most faithful alignment to pillar geometries with smallest gap sizes. Neurite lengths were significantly longer on pillars with the smallest inter-pillar spacings (gaps) and 2 mu m pillar widths. These data indicate that physical cues affect neuron growth, suggesting that extracellular matrix topography may contribute to cell growth and differentiation. These results demonstrate new strategies for directing and promoting neuronal growth that will facilitate studies of synapse formation and function and provide methods to establish defined neural networks.
引用
收藏
页码:78 / 90
页数:13
相关论文
共 51 条
[1]   Automated tracing and change analysis of angiogenic vasculature from in vivo multiphoton confocal image time series [J].
Abdul-Karim, MA ;
Al-Kofahi, K ;
Brown, EB ;
Jain, RK ;
Roysam, B .
MICROVASCULAR RESEARCH, 2003, 66 (02) :113-125
[2]  
Abrams GA, 2000, CELL TISSUE RES, V299, P39, DOI 10.1007/s004410050004
[3]   Rapid automated three-dimensional tracing of neurons from confocal image stacks [J].
Al-Kofahi, KA ;
Lasek, S ;
Szarowski, DH ;
Pace, CJ ;
Nagy, G ;
Turner, JN ;
Roysam, B .
IEEE TRANSACTIONS ON INFORMATION TECHNOLOGY IN BIOMEDICINE, 2002, 6 (02) :171-187
[4]   Algorithms for accurate 3D registration of neuronal images acquired by confocal scanning laser microscopy [J].
Al-Kofahi, O ;
Can, A ;
Lasek, S ;
Szarowski, DH ;
Turner, JN ;
Roysam, B .
JOURNAL OF MICROSCOPY, 2003, 211 :8-18
[5]   IDENTIFICATION OF THE MAJOR PROTEINS THAT PROMOTE NEURONAL PROCESS OUTGROWTH ON SCHWANN-CELLS INVITRO [J].
BIXBY, JL ;
LILIEN, J ;
REICHARDT, LF .
JOURNAL OF CELL BIOLOGY, 1988, 107 (01) :353-361
[6]   OPTIMIZED SURVIVAL OF HIPPOCAMPAL-NEURONS IN B27-SUPPLEMENTED NEUROBASAL(TM), A NEW SERUM-FREE MEDIUM COMBINATION [J].
BREWER, GJ ;
TORRICELLI, JR ;
EVEGE, EK ;
PRICE, PJ .
JOURNAL OF NEUROSCIENCE RESEARCH, 1993, 35 (05) :567-576
[7]  
Britland S, 1996, EXP BIOL ONLINE, V1, P2
[8]  
Can A, 1999, IEEE Trans Inf Technol Biomed, V3, P125, DOI 10.1109/4233.767088
[9]  
CLARK P, 1990, DEVELOPMENT, V108, P635
[10]  
CLARK P, 1991, J CELL SCI, V99, P73