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dc.contributor.authorXu, Chenjie
dc.contributor.authorPoh, Yuk Kee C.
dc.contributor.authorRoes, Isaac Victor
dc.contributor.authorO'Cearbhaill, Eoin D.
dc.contributor.authorMatthiesen, Mads Emil
dc.contributor.authorMu, Luye
dc.contributor.authorYang, Seung Yun
dc.contributor.authorMiranda-Nieves, David
dc.contributor.authorIrimia, Daniel
dc.contributor.authorKarp, Jeffrey Michael
dc.date.accessioned2013-01-23T21:36:00Z
dc.date.available2013-01-23T21:36:00Z
dc.date.issued2012-09
dc.date.submitted2012-01
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/76587
dc.description.abstractFlow-based microfluidic systems have been widely utilized for cell migration studies given their ability to generate versatile and precisely defined chemical gradients and to permit direct visualization of migrating cells. Nonetheless, the general need for bulky peripherals such as mechanical pumps and tubing and the complicated setup procedures significantly limit the widespread use of these microfluidic systems for cell migration studies. Here we present a simple method to power microfluidic devices for chemotaxis assays using the commercially available ALZET® osmotic pumps. Specifically, we developed a standalone chemotaxis platform that has the same footprint as a multiwell plate and can generate well-defined, stable chemical gradients continuously for up to 7 days. Using this platform, we validated the short-term (24 hours) and long-term (72 hours) concentration dependent PDGF-BB chemotaxis response of human bone marrow derived mesenchymal stem cells.en_US
dc.description.sponsorshipHarvard Stem Cell Instituteen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant HL095722)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant HL097172)en_US
dc.description.sponsorshipMassachusetts Institute of Technology (MIT-UROP program)en_US
dc.description.sponsorshipMassachusetts Institute of Technology (John Reed Fund)en_US
dc.description.sponsorshipNational Institute of Biomedical Imaging and Bioengineering (U.S.) (BioMEMS Resource Center (P41 EB 002503))en_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0044995en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/en_US
dc.sourcePLoSen_US
dc.titleA Portable Chemotaxis Platform for Short and Long Term Analysisen_US
dc.typeArticleen_US
dc.identifier.citationXu, Chenjie et al. “A Portable Chemotaxis Platform for Short and Long Term Analysis.” Ed. Jianghong Rao. PLoS ONE 7.9 (2012): e44995. Web.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.mitauthorXu, Chenjie
dc.contributor.mitauthorPoh, Yuk Kee C.
dc.contributor.mitauthorRoes, Isaac Victor
dc.contributor.mitauthorO'Cearbhaill, Eoin D.
dc.contributor.mitauthorMatthiesen, Mads Emil
dc.contributor.mitauthorMu, Luye
dc.contributor.mitauthorYang, Seung Yun
dc.contributor.mitauthorMiranda-Nieves, David
dc.contributor.mitauthorKarp, Jeffrey Michael
dc.relation.journalPLoS Oneen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsXu, Chenjie; Poh, Yuk Kee C.; Roes, Isaac; O'Cearbhaill, Eoin D.; Matthiesen, Mads Emil; Mu, Luye; Yang, Seung Yun; Miranda-Nieves, David; Irimia, Daniel; Karp, Jeffrey M.en
dc.identifier.orcidhttps://orcid.org/0000-0003-3209-8519
dc.identifier.orcidhttps://orcid.org/0000-0002-3253-7799
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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