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dc.contributor.authorVoldman, Joel
dc.contributor.authorPrzybyla, Laralynne M.
dc.date.accessioned2014-10-21T14:39:52Z
dc.date.available2014-10-21T14:39:52Z
dc.date.issued2012-04
dc.identifier.issn1936-1327
dc.identifier.issn1936-1335
dc.identifier.urihttp://hdl.handle.net/1721.1/91017
dc.description.abstractAlthough stem cell fate is traditionally manipulated by exogenously altering the cells' extracellular signaling environment, the endogenous autocrine and paracrine signals produced by the cells also contribute to their two essential processes: self-renewal and differentiation. Autocrine and/or paracrine signals are fundamental to both embryonic stem cell self-renewal and early embryonic development, but the nature and contributions of these signals are often difficult to fully define using conventional methods. Microfluidic techniques have been used to explore the effects of cell-secreted signals by controlling cell organization or by providing precise control over the spatial and temporal cellular microenvironment. Here we review how such techniques have begun to be adapted for use with embryonic stem cells, and we illustrate how many remaining questions in embryonic stem cell biology could be addressed using microfluidic technologies.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (EB007278)en_US
dc.description.sponsorshipSingapore-MIT Allianceen_US
dc.description.sponsorshipNational Science Foundation (U.S.) (0939511)en_US
dc.language.isoen_US
dc.publisherAnnual Reviewsen_US
dc.relation.isversionofhttp://dx.doi.org/10.1146/annurev-anchem-062011-143122en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleProbing Embryonic Stem Cell Autocrine and Paracrine Signaling Using Microfluidicsen_US
dc.typeArticleen_US
dc.identifier.citationPrzybyla, Laralynne, and Joel Voldman. “Probing Embryonic Stem Cell Autocrine and Paracrine Signaling Using Microfluidics.” Annual Review of Analytical Chemistry 5, no. 1 (July 19, 2012): 293–315.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.mitauthorPrzybyla, Laralynneen_US
dc.contributor.mitauthorVoldman, Joelen_US
dc.relation.journalAnnual Review of Analytical Chemistryen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsPrzybyla, Laralynne; Voldman, Joelen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-8898-2296
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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