Macrefabricated multilayer parylene-C stencils for the generation of patterned dynamic co-cultures

被引:45
作者
Jinno, Satoshi [1 ,2 ,5 ]
Moeller, Hannes-Christian [1 ,3 ]
Chen, Chia-Ling [4 ]
Rajalingam, Bimal [1 ,5 ]
Chung, Bong Geun [1 ,5 ]
Dokmeci, Mehmet R. [4 ]
Khademhosseini, Ali [1 ,5 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med,Ctr Biomed Engn, Boston, MA 02115 USA
[2] Aichi Gakuin Univ, Sch Dent, Dept Periodontol, Nagoya, Aichi 464, Japan
[3] Ecole Super Biotechnol Strasbourg, F-67412 Illkirch Graffenstaden, France
[4] Northeastern Univ, Ctr High Rate Nanomfg, Dept Elect & Comp Engn, Boston, MA 02115 USA
[5] MIT, Harvard MIT Div Hlth Sci & Technol, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
cellular microenvironment; dynamic co-culture; parylene-C stencils; cell patterning;
D O I
10.1002/jbm.a.32030
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Co-culturing different cell types can be useful to engineer a more in vivo-like microenvironment for cells in culture. Recent approaches to generating cellular co-cultures have used microfabrication technologies to regulate the degree of cell-cell contact between different cell types. However, these approaches are often limited to the co-culture of only two cell types in static cultures. The dynamic aspect of cell-cell interaction, however, is a key regulator of many biological processes such as early development, stem cell differentiation, and tissue regeneration. In this study, we describe a micropatterning technique based on microfabricated multilayer parylene-C stencils and demonstrate the potential of parylene-C technology for co-patterning of proteins and cells with the ability to generate a series of at least five temporally controlled patterned cocultures. We generated dynamic co-cultures of murine embryonic stem cells in culture with various secondary cell types that could be sequentially introduced and removed from the co-cultures. Our studies suggested that dynamic co-cultures generated by using parylene-C stencils may be applicable in studies investigating cellular interactions in controlled microenvironments such as studies of ES cell differentiation, wound healing and development. (c) 2008 Wiley Periodicals, Inc.
引用
收藏
页码:278 / 288
页数:11
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