Using continuous porous silicon gradients to study the influence of surface topography on the behaviour of neuroblastoma cells

被引:97
作者
Khung, Y. L. [1 ]
Barritt, G. [2 ]
Voelcker, N. H. [1 ]
机构
[1] Flinders Univ S Australia, Sch Chem Phys & Earth Sci, Adelaide, SA 5001, Australia
[2] Flinders Univ S Australia, Sch Med, Dept Med Biochem, Adelaide, SA 5001, Australia
基金
澳大利亚研究理事会;
关键词
porous silicon; cell material interactions; topographical gradients;
D O I
10.1016/j.yexcr.2007.10.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The effects of surface topography on cell behaviour are the subject of intense research in cell biology. These effects have so far only been studied using substrate surfaces of discretely different topography. in this paper, we present a new approach to characterise cell growth on porous silicon gradients displaying pore sizes from several thousands to a few nanometers. This widely applicable format has the potential to significantly reduce sample numbers and hence analysis time and cost. Our gradient format was applied here to the culture of neuroblastoma cells in order to determine the effects of topography on cell growth parameters. Cell viability, morphology, length and area were characterised by fluorescence and scanning electron microscopy. We observed a dramatic influence of changes in surface topography on the density and morphology of adherent neuroblastoma cells. For example, pore size regimes where cell attachment is strongly discouraged were identified providing cues for the design of low-fouling surfaces. On pore size regimes more conducive to cell attachment, lateral cell-cell interactions crosslinked the cell layer to the substratum surface, while direct substrate-cell interactions were scarce. Finally, our study revealed that cells were sensitive to nanoscale surface topography with feature sizes of < 20 nm. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:789 / 800
页数:12
相关论文
共 71 条
[1]   Porosity variation in hydroxyapatite and osteoblast morphology: a scanning electron microscopy study [J].
Annaz, B ;
Hing, KA ;
Kayser, M ;
Buckland, T ;
Di Silvio, L .
JOURNAL OF MICROSCOPY, 2004, 215 :100-110
[2]  
ANTHONY JK, 2003, SCI STKE, pPE20
[3]   SHAPE CHANGES OF THE HUMAN RED-CELL STUDIED BY AQUEOUS 2-PHASE PARTITION [J].
BACKMAN, L .
FEBS LETTERS, 1990, 262 (01) :107-110
[4]   THE FINE-STRUCTURE OF CONTINUOUS HUMAN NEURO-BLASTOMA LINES SK-N-SH, SK-N-BE(2), AND SK-N-MC [J].
BARNES, EN ;
BIEDLER, JL ;
SPENGLER, BA ;
LYSER, KM .
IN VITRO-JOURNAL OF THE TISSUE CULTURE ASSOCIATION, 1981, 17 (07) :619-631
[5]   Nature of the silicon-animal cell interface [J].
Bayliss, SC ;
Buckberry, LD ;
Harris, PJ ;
Tobin, M .
JOURNAL OF POROUS MATERIALS, 2000, 7 (1-3) :191-195
[6]  
Bayliss SC, 1999, ADV MATER, V11, P318, DOI 10.1002/(SICI)1521-4095(199903)11:4<318::AID-ADMA318>3.0.CO
[7]  
2-Z
[8]   The culture of neurons on silicon [J].
Bayliss, SC ;
Buckberry, LD ;
Fletcher, I ;
Tobin, MJ .
SENSORS AND ACTUATORS A-PHYSICAL, 1999, 74 (1-3) :139-142
[9]  
BECKER JW, 1989, P NATL ACAD SCI USA, V86, P5670
[10]   Attenuation of δ opioid receptor-mediated signaling by kainic acid in neural cells:: involvement of protein kinase C and intracellular Ca2+ [J].
Ben, LH ;
Zhao, J ;
Xin, SM ;
Luo, SQ ;
Pei, G .
NEUROPHARMACOLOGY, 1999, 38 (07) :991-998