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Nanoliter Liquid Patterning in Aqueous Environments for Spatially-Defined Reagent Delivery to Mammalian Cells
Microscale biopatterning allows regulation of cell-material interactions1,2 and cell shape3, and enables multiplexed high throughput studies4,5,6,7,8 in a cell and reagent efficient manner. The majority of available techniques rely on physical contact of a stamp3, pin8, or mask9,10 with mainly a dry...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782768/ https://www.ncbi.nlm.nih.gov/pubmed/19684584 http://dx.doi.org/10.1038/nmat2515 |
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author | Tavana, H. Jovic, A. Mosadegh, B. Lee, Q. Y. Liu, X. Luker, K.E. Luker, G.D. Weiss, S. J. Takayama, S. |
author_facet | Tavana, H. Jovic, A. Mosadegh, B. Lee, Q. Y. Liu, X. Luker, K.E. Luker, G.D. Weiss, S. J. Takayama, S. |
author_sort | Tavana, H. |
collection | PubMed |
description | Microscale biopatterning allows regulation of cell-material interactions1,2 and cell shape3, and enables multiplexed high throughput studies4,5,6,7,8 in a cell and reagent efficient manner. The majority of available techniques rely on physical contact of a stamp3, pin8, or mask9,10 with mainly a dry surface. Inkjet and piezoelectric printing11 is performed in a non-contact manner but still requires a substantially dry substrate to ensure fidelity of printed patterns. These existing methods, therefore, are limited for patterning onto delicate surfaces of living cells because physical contact or substantially dry conditions are damaging to them. Microfluidic patterning with laminar streams12,13 does allow non-contact patterning in fully aqueous environments but with limited throughput and reagent diffusion across interfacial flows. Here, we describe a polymeric aqueous two-phase system (ATPS) that enables patterning nanoliters of a reagent-containing aqueous phase, in arbitrary shapes, within a second aqueous phase covering a cell monolayer. With the appropriate media formulation, reagents of interest remain confined to the patterned phase without significant diffusion. The fully aqueous environment ensures high reagent activity and cell viability. Utility of this strategy is demonstrated with patterned delivery of genetic materials to mammalian cells for phenotypic screening of gene expression and gene silencing. |
format | Text |
id | pubmed-2782768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
record_format | MEDLINE/PubMed |
spelling | pubmed-27827682010-03-01 Nanoliter Liquid Patterning in Aqueous Environments for Spatially-Defined Reagent Delivery to Mammalian Cells Tavana, H. Jovic, A. Mosadegh, B. Lee, Q. Y. Liu, X. Luker, K.E. Luker, G.D. Weiss, S. J. Takayama, S. Nat Mater Article Microscale biopatterning allows regulation of cell-material interactions1,2 and cell shape3, and enables multiplexed high throughput studies4,5,6,7,8 in a cell and reagent efficient manner. The majority of available techniques rely on physical contact of a stamp3, pin8, or mask9,10 with mainly a dry surface. Inkjet and piezoelectric printing11 is performed in a non-contact manner but still requires a substantially dry substrate to ensure fidelity of printed patterns. These existing methods, therefore, are limited for patterning onto delicate surfaces of living cells because physical contact or substantially dry conditions are damaging to them. Microfluidic patterning with laminar streams12,13 does allow non-contact patterning in fully aqueous environments but with limited throughput and reagent diffusion across interfacial flows. Here, we describe a polymeric aqueous two-phase system (ATPS) that enables patterning nanoliters of a reagent-containing aqueous phase, in arbitrary shapes, within a second aqueous phase covering a cell monolayer. With the appropriate media formulation, reagents of interest remain confined to the patterned phase without significant diffusion. The fully aqueous environment ensures high reagent activity and cell viability. Utility of this strategy is demonstrated with patterned delivery of genetic materials to mammalian cells for phenotypic screening of gene expression and gene silencing. 2009-08-16 2009-09 /pmc/articles/PMC2782768/ /pubmed/19684584 http://dx.doi.org/10.1038/nmat2515 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Tavana, H. Jovic, A. Mosadegh, B. Lee, Q. Y. Liu, X. Luker, K.E. Luker, G.D. Weiss, S. J. Takayama, S. Nanoliter Liquid Patterning in Aqueous Environments for Spatially-Defined Reagent Delivery to Mammalian Cells |
title | Nanoliter Liquid Patterning in Aqueous Environments for Spatially-Defined Reagent Delivery to Mammalian Cells |
title_full | Nanoliter Liquid Patterning in Aqueous Environments for Spatially-Defined Reagent Delivery to Mammalian Cells |
title_fullStr | Nanoliter Liquid Patterning in Aqueous Environments for Spatially-Defined Reagent Delivery to Mammalian Cells |
title_full_unstemmed | Nanoliter Liquid Patterning in Aqueous Environments for Spatially-Defined Reagent Delivery to Mammalian Cells |
title_short | Nanoliter Liquid Patterning in Aqueous Environments for Spatially-Defined Reagent Delivery to Mammalian Cells |
title_sort | nanoliter liquid patterning in aqueous environments for spatially-defined reagent delivery to mammalian cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782768/ https://www.ncbi.nlm.nih.gov/pubmed/19684584 http://dx.doi.org/10.1038/nmat2515 |
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