Using continuous porous silicon gradients to study the influence of surface topography on the behaviour of neuroblastoma cells
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 gra...
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| Published in | Experimental cell research Vol. 314; no. 4; pp. 789 - 800 |
|---|---|
| Main Authors | , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Elsevier Inc
15.02.2008
Elsevier BV |
| Subjects | |
| Online Access | Get full text |
| ISSN | 0014-4827 1090-2422 |
| DOI | 10.1016/j.yexcr.2007.10.015 |
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| Abstract | 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. |
|---|---|
| AbstractList | 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. 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.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. 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. [PUBLICATION ABSTRACT] 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. |
| Author | Barritt, G. Khung, Y.L. Voelcker, N.H. |
| Author_xml | – sequence: 1 givenname: Y.L. surname: Khung fullname: Khung, Y.L. organization: School of Chemistry, Physics and Earth Sciences, Flinders University, GPO Box 2100, Adelaide 5001, South Australia, Australia – sequence: 2 givenname: G. surname: Barritt fullname: Barritt, G. organization: Department of Medical Biochemistry, School of Medicine, Flinders University, GPO Box 2100, Adelaide 5001, South Australia, Australia – sequence: 3 givenname: N.H. surname: Voelcker fullname: Voelcker, N.H. email: nico.voelcker@flinders.edu.au organization: School of Chemistry, Physics and Earth Sciences, Flinders University, GPO Box 2100, Adelaide 5001, South Australia, Australia |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18054914$$D View this record in MEDLINE/PubMed https://www.osti.gov/biblio/21045940$$D View this record in Osti.gov |
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| SubjectTerms | 60 APPLIED LIFE SCIENCES Cell Count Cell growth Cell Line, Tumor Cell material interactions Cell Proliferation Cells Cellular biology CROSS-LINKING FLUORESCENCE Humans Microscopy, Confocal Microscopy, Electron, Scanning Microscopy, Fluorescence MORPHOLOGY NANOSTRUCTURES Nanostructures - chemistry Nanotechnology Neuroblastoma Neurons - cytology Neurons - ultrastructure POROUS MATERIALS Porous silicon Pseudopodia - ultrastructure SCANNING ELECTRON MICROSCOPY SILICON Silicon - chemistry SUBSTRATES Surface Properties Topographical gradients |
| Title | Using continuous porous silicon gradients to study the influence of surface topography on the behaviour of neuroblastoma cells |
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