These authors contributed equally to this work.
Microfabricated multilayer parylene-C stencils for the generation of patterned dynamic co-cultures
Article first published online: 28 APR 2008
DOI: 10.1002/jbm.a.32030
Copyright © 2008 Wiley Periodicals, Inc.
Additional Information
How to Cite
Jinno, S., Moeller, H.-C., Chen, C.-L., Rajalingam, B., Chung, B. G., Dokmeci, M. R. and Khademhosseini, A. (2008), Microfabricated multilayer parylene-C stencils for the generation of patterned dynamic co-cultures. Journal of Biomedical Materials Research Part A, 86A: 278–288. doi: 10.1002/jbm.a.32030
Publication History
- Issue published online: 20 MAY 2008
- Article first published online: 28 APR 2008
- Manuscript Accepted: 14 FEB 2008
- Manuscript Received: 11 FEB 2008
Funded by
- Coulter Foundation
- National Institutes of Health (NIH)
- Center for Integration of Medicine and Innovative Technology (CIMIT)
- Institute for Soldier Nanotechnology (ISN)
- Charles Stark Draper Laboratory
- Abstract
- Article
- References
- Cited By
Keywords:
- cellular microenvironment;
- dynamic co-culture;
- parylene-C stencils;
- cell patterning
Abstract
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 co-cultures. 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. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res, 2008

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