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dc.contributor.authorBerger, Christoph T.
dc.contributor.authorSips, Magdalena
dc.contributor.authorCheney, Patrick C.
dc.contributor.authorAlter, Galit
dc.contributor.authorYamanaka, Yvonne J.
dc.contributor.authorLove, John C
dc.date.accessioned2013-07-18T15:39:41Z
dc.date.available2013-07-18T15:39:41Z
dc.date.issued2012-08
dc.date.submitted2012-07
dc.identifier.issn1757-9694
dc.identifier.issn1757-9708
dc.identifier.urihttp://hdl.handle.net/1721.1/79616
dc.description.abstractNatural killer (NK) cells are a subset of innate immune lymphocytes that interrogate potential target cells and rapidly respond by lysing them or secreting inflammatory immunomodulators. Productive interactions between NK cells and targets such as tumor cells or virally infected cells are critical for immunological control of malignancies and infections. For individual NK cells, however, the relationship between the characteristics of these cell–cell interactions, cytolysis, and secretory activity is not well understood. Here, we used arrays of subnanoliter wells (nanowells) to monitor individual NK cell–target cell interactions and quantify the resulting cytolytic and secretory responses. We show that NK cells operate independently when lysing a single target cell and that lysis is most probable during an NK cell's first encounter with a target. Furthermore, we demonstrate that the secretion of interferon-γ (IFN-γ) occurs most often among NK cells that become the least motile upon contacting a target cell but is largely independent of cytolysis. Our findings demonstrate that integrated analysis of the cell–cell interaction parameters, cytolytic activity, and secretory activity of single NK cells can reveal new insights into how these complex functions are related within individual cells.en_US
dc.description.sponsorshipCharles A. Dana Foundationen_US
dc.description.sponsorshipW. M. Keck Foundationen_US
dc.description.sponsorshipRagon Institute of MGH, MIT and Harvarden_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Fellowship)en_US
dc.description.sponsorshipMassachusetts Institute of Technology (Collamore-Rogers Fellowship)en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/c2ib20167den_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourceProf. Love via Erja Kajosaloen_US
dc.titleSingle-cell analysis of the dynamics and functional outcomes of interactions between human natural killer cells and target cellsen_US
dc.typeArticleen_US
dc.identifier.citationYamanaka, Yvonne J., Christoph T. Berger, Magdalena Sips, et al. 2012 Single-cell Analysis of the Dynamics and Functional Outcomes of Interactions Between Human Natural Killer Cells and Target Cells. Integrative Biology 4(10): 1175.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentRagon Institute of MGH, MIT and Harvarden_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.approverLove, J. Christopheren_US
dc.contributor.mitauthorLove, J. Christopheren_US
dc.contributor.mitauthorYamanaka, Yvonne Joyen_US
dc.contributor.mitauthorBerger, Christoph T.en_US
dc.contributor.mitauthorSips, Magdalenaen_US
dc.contributor.mitauthorCheney, Patrick C.en_US
dc.contributor.mitauthorAlter, Galiten_US
dc.relation.journalIntegrative Biologyen_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.orderedauthorsYamanaka, Yvonne J.; Berger, Christoph T.; Sips, Magdalena; Cheney, Patrick C.; Alter, Galit; Love, J. Christopheren_US
dc.identifier.orcidhttps://orcid.org/0000-0003-0921-3144
dc.identifier.orcidhttps://orcid.org/0000-0003-1570-9445
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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