A Hollow Sphere Soft Lithography Approach for Long-Term Hanging Drop Methods

In conventional hanging drop (HD) methods, embryonic stem cell aggregates or embryoid bodies (EBs) are often maintained in small inverted droplets. Gravity limits the volumes of these droplets to less than 50 μL [mu L], and hence such cell cultures can only be sustained for a few days without freque...

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Bibliographic Details
Main Authors: Lee, Won Gu (Contributor), Ortmann, Daniel (Contributor), Hancock, Matthew J. (Contributor), Bae, Hojae (Contributor), Khademhosseini, Ali (Contributor)
Other Authors: Harvard University- (Contributor)
Format: Article
Language:English
Published: Mary Ann Liebert, 2011-03-04T18:21:05Z.
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Online Access:Get fulltext
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100 1 0 |a Lee, Won Gu  |e author 
100 1 0 |a Harvard University-  |e contributor 
100 1 0 |a Khademhosseini, Ali  |e contributor 
100 1 0 |a Lee, Won Gu  |e contributor 
100 1 0 |a Ortmann, Daniel  |e contributor 
100 1 0 |a Hancock, Matthew J.  |e contributor 
100 1 0 |a Bae, Hojae  |e contributor 
100 1 0 |a Khademhosseini, Ali  |e contributor 
700 1 0 |a Ortmann, Daniel  |e author 
700 1 0 |a Hancock, Matthew J.  |e author 
700 1 0 |a Bae, Hojae  |e author 
700 1 0 |a Khademhosseini, Ali  |e author 
245 0 0 |a A Hollow Sphere Soft Lithography Approach for Long-Term Hanging Drop Methods 
260 |b Mary Ann Liebert,   |c 2011-03-04T18:21:05Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/61412 
520 |a In conventional hanging drop (HD) methods, embryonic stem cell aggregates or embryoid bodies (EBs) are often maintained in small inverted droplets. Gravity limits the volumes of these droplets to less than 50 μL [mu L], and hence such cell cultures can only be sustained for a few days without frequent media changes. Here we present a new approach to performing long-term HD methods (10-15 days) that can provide larger media reservoirs in a HD format to maintain more consistent culture media conditions. To implement this approach, we fabricated hollow sphere (HS) structures by injecting liquid drops into noncured poly(dimethylsiloxane) mixtures. These structures served as cell culture chambers with large media volumes (500 μL [mu L] in each sphere) where EBs could grow without media depletion. The results showed that the sizes of the EBs cultured in the HS structures in a long-term HD format were approximately twice those of conventional HD methods after 10 days in culture. Further, HS cultures showed multilineage differentiation, similar to EBs cultured in the HD method. Due to its ease of fabrication and enhanced features, this approach may be of potential benefit as a stem cell culture method for regenerative medicine. 
520 |a National Institutes of Health (U.S.) (DE019024) (HL092836) (EB007249) 
520 |a Korean Research Foundation (Grant KRF-2007-357-D00035) 
520 |a German Academic Exchange Service 
546 |a en_US 
655 7 |a Article 
773 |t Tissue Engineering. Part C, Methods