期刊论文详细信息
Journal of Nanobiotechnology
Bioimprinted polymer platforms for cell culture using soft lithography
Maan M Alkaisi2  John J Evans1  Volker Nock2  Lynn M Murray2 
[1] The MacDiarmid Institute for Advanced Materials and Nanotechnology, and Centre for Neuroendocrinology, Department of Obstetrics and Gynaecology, University of Otago, Christchurch 8011, New Zealand;The MacDiarmid Institute for Advanced Materials and Nanotechnology, Department of Electrical and Computer Engineering, University of Canterbury, Christchurch 8140, New Zealand
关键词: Cell microenvironment;    Surface topography;    Soft lithography;    Cancer cell;    Cell culture platform;    Bioimprint;   
Others  :  1137470
DOI  :  10.1186/s12951-014-0060-6
 received in 2014-08-05, accepted in 2014-12-12,  发布年份 2014
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【 摘 要 】

Background

It is becoming recognised that traditional methods of culture in vitro on flat substrates do not replicate physiological conditions well, and a number of studies have indicated that the physical environment is crucial to the directed functioning of cells in vivo. In this paper we report the development of a platform with cell-like features that is suitable for in vitro investigation of cell activity. Biological cells were imprinted in hard methacrylate copolymer using soft lithography. The cell structures were replicated at high nanometre scale resolution, as confirmed by atomic force microscopy. Optimisation of the methacrylate-based co-polymer mixture for transparency and biocompatibility was performed, and cytotoxicity and chemical stability of the cured polymer in cell culture conditions were evaluated. Cells of an endometrial adenocarcinoma cell line (Ishikawa) were cultured on bioimprinted substrates.

Results

The cells exhibited differential attachment on the bioimprint substrate surface compared to those on areas of flat surface and preferentially followed the pattern of the original cell footprint.

Conclusions

The results revealed for the first time that the cancer cells distinguished between behavioural cues from surfaces that had features reminiscent of themselves and that of flat areas. Therefore the imprinted platform will lend itself to detailed studies of relevant physical substrate environments on cell behaviour. The material is not degraded and its permanency allows reuse of the same substrate in multiple experimental runs. It is simple and does not require expensive or specialised equipment. In this work cancer cells were studied, and the growth behaviour of the tumour-derived cells was modified by alterations of the cells’ physical environment. Implications are also clear for studies in other crucial areas of health, such as wound healing and artificial tissues.

【 授权许可】

   
2015 Murray et al.; licensee BioMed Central.

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【 参考文献 】
  • [1]Mills AM, Longacre TA: Endometrial hyperplasia. Semin Diagn Pathol 2010, 27:199-214.
  • [2]Bhattacharya N: Fetal cell/tissue therapy in adult disease: a new horizon in regenerative medicine. Clin Exp Obstet Gynecol 2004, 31:167-173.
  • [3]Longmate WM, Dipersio CM: Integrin regulation of epidermal functions in wounds. Adv Wound Care 2014, 3:229-246.
  • [4]Lindstrom S, Andersson-Svahn H: Overview of single-cell analyses: microdevices and applications. Lab Chip 2010, 10:3363-3372.
  • [5]Kraning-Rush CM, Reinhart-King CA: Controlling matrix stiffness and topography for the study of tumor cell migration. Cell Adh Migr 2012, 6:274-279.
  • [6]Blattler T, Huwiler C, Ochsner M, Stadler B, Solak H, Voros J, Grandin HM: Nanopatterns with biological functions. J Nanosci Nanotechnol 2006, 6:2237-2264.
  • [7]Lan H, Liu H: UV-nanoimprint lithography: structure, materials and fabrication of flexible molds. J Nanosci Nanotechnol 2013, 13:3145-3172.
  • [8]Biggs MJ, Richards RG, Dalby MJ: Nanotopographical modification: a regulator of cellular function through focal adhesions. Nanomed 2010, 6:619-633.
  • [9]Nikkhah M, Edalat F, Manoucheri S, Khademhosseini A: Engineering microscale topographies to control the cell-substrate interface. Biomaterials 2012, 33:5230-5246.
  • [10]Muys JJ, Alkaisi MM, Evans JJ: Cancer imaging by atomic force microscopy using a bioimprint cellular transfer technique. J Nanobiotechnol 2005, 4(1):10.
  • [11]Muys JJ, Alkaisi MM, Evans JJ: Bioimprint: nanoscale analysis by replication of cellular topography using soft lithography. J Biomed Nanotechnol 2006, 2:1-5.
  • [12]Murray LM, Nock V, Alkaisi MM, Lee JJM, Woodfield TBF: Fabrication of polymeric substrates with micro- and nanoscale topography bioimprinted at progressive cell morphologies.J Va Sci & Technol B: Microelectron and Nanometer Struct 2012, 30:06F902–906F902–906.
  • [13]Nock V, Murray L, Samsuri F, Alkaisi MM, Evans JJ: Microfluidics-assisted photo nanoimprint lithography for the formation of cellular bioimprints.J Vac Sci & Technol B 2010, 28:C6K17–C16K22.
  • [14]Nock V, Murray L, Samsuri F, Alkaisi MM, Evans JJ: Microfluidic arrays for bioimprint of cancer cells. Microelectron Eng 2011, 88:1828-1831.
  • [15]Wang X, Zhang Y, Du K, Fang X: Atomic force microscope observation on ultrastructures in plant cells. J Nanosci Nanotechnol 2010, 10:6624-6628.
  • [16]Li JJ, Zhou XT, Shi J, Zhang F, Li X, Jiang LM, Chen Y: Upside and downside views of adherent cells on patterned substrates: three-dimensional image reconstruction. Microelectron Eng 2013, 110:365-368.
  • [17]Samsuri F, Mitchell JS, Alkaisi MM, Evans JJ: Formation of Nanoscale Bioimprints of Muscle Cells Using UV-Cured Spin-Coated Polymers. J Nanotech 2009, 2009:6.
  • [18]Samsuri F, Alkaisi MM, Evans JJ, Chitcholtan K, Mitchell JS: Detection of changes in cell membrane structures using the Bioimprint technique. Microelectron Eng 2011, 88:1871-1874.
  • [19]DePorter SM, Luib I, McNaughton BR: Programmed cell adhesion and growth on cell-imprinted polyacrylamide hydrogels. Soft Matter 2012, 8:10403-10408.
  • [20]Jeon H, Kim G: Effects of a cell-imprinted poly(dimethylsiloxane) surface on the cellular activities of MG63 osteoblast-like cells: preparation of a patterned surface, surface characterization, and bone mineralization. Langmuir 2012, 28:13423-13430.
  • [21]Tong WY, Shen W, Yeung CW, Zhao Y, Cheng SH, Chu PK, Chan D, Chan GC, Cheung KM, Yeung KW, Lam YW: Functional replication of the tendon tissue microenvironment by a bioimprinted substrate and the support of tenocytic differentiation of mesenchymal stem cells. Biomaterials 2012, 33:7686-7698.
  • [22]Spivaka DA, Shea KJ: Investigation into the scope and limitations of molecular imprinting with DNA molecules. Anal Chim Acta 2001, 435:65-74.
  • [23]Bolisay LD, Culver JN, Kofinas P: Molecularly imprinted polymers for tobacco mosaic virus recognition. Biomaterials 2006, 27:4165-4168.
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