Three-dimensional tissue culture based on magnetic cell levitation

被引:0
|
作者
Glauco R. Souza
Jennifer R. Molina
Robert M. Raphael
Michael G. Ozawa
Daniel J. Stark
Carly S. Levin
Lawrence F. Bronk
Jeyarama S. Ananta
Jami Mandelin
Maria-Magdalena Georgescu
James A. Bankson
Juri G. Gelovani
T. C. Killian
Wadih Arap
Renata Pasqualini
机构
[1] David H. Koch Center,Department of Neuro
[2] The University of Texas M.D. Anderson Cancer Center,Oncology
[3] The University of Texas M.D. Anderson Cancer Center,Department of Bioengineering
[4] Rice University,Department of Physics and Astronomy
[5] Rice University,Department of Chemistry
[6] Nano3D Biosciences,Department of Imaging Physics
[7] Inc.,Department of Experimental Diagnostic Imaging
[8] Rice University,undefined
[9] The University of Texas M.D. Anderson Cancer Center,undefined
[10] The University of Texas M.D. Anderson Cancer Center,undefined
[11] Present address: Nano3D Biosciences,undefined
[12] Inc.,undefined
[13] Houston,undefined
[14] Texas 77030,undefined
[15] USA,undefined
来源
Nature Nanotechnology | 2010年 / 5卷
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摘要
Cell culture is an essential tool in drug discovery, tissue engineering and stem cell research. Conventional tissue culture produces two-dimensional cell growth with gene expression, signalling and morphology that can be different from those found in vivo, and this compromises its clinical relevance1,2,3,4,5. Here, we report a three-dimensional tissue culture based on magnetic levitation of cells in the presence of a hydrogel consisting of gold, magnetic iron oxide nanoparticles and filamentous bacteriophage. By spatially controlling the magnetic field, the geometry of the cell mass can be manipulated, and multicellular clustering of different cell types in co-culture can be achieved. Magnetically levitated human glioblastoma cells showed similar protein expression profiles to those observed in human tumour xenografts. Taken together, these results indicate that levitated three-dimensional culture with magnetized phage-based hydrogels more closely recapitulates in vivo protein expression and may be more feasible for long-term multicellular studies.
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页码:291 / 296
页数:5
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