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dc.contributor.authorMaloney, John M.
dc.contributor.authorNikova, Dessy
dc.contributor.authorLautenschläger, Franziska
dc.contributor.authorClarke, Emer
dc.contributor.authorLanger, Robert
dc.contributor.authorGuck, Jochen
dc.contributor.authorVan Vliet, Krystyn J.
dc.date.accessioned2015-03-17T15:36:40Z
dc.date.available2015-03-17T15:36:40Z
dc.date.issued2010-10
dc.date.submitted2010-05
dc.identifier.issn00063495
dc.identifier.issn1542-0086
dc.identifier.urihttp://hdl.handle.net/1721.1/96041
dc.description.abstractHuman mesenchymal stem cells (hMSCs) are therapeutically useful cells that are typically expanded in vitro on stiff substrata before reimplantation. Here we explore MSC mechanical and structural changes via atomic force microscopy and optical stretching during extended passaging, and we demonstrate that cytoskeletal organization and mechanical stiffness of attached MSC populations are strongly modulated over >15 population doublings in vitro. Cytoskeletal actin networks exhibit significant coarsening, attendant with decreasing average mechanical compliance and differentiation potential of these cells, although expression of molecular surface markers does not significantly decline. These mechanical changes are not observed in the suspended state, indicating that the changes manifest themselves as alterations in stress fiber arrangement rather than cortical cytoskeleton arrangement. Additionally, optical stretching is capable of investigating a previously unquantified structural transition: remodeling-induced stiffening over tens of minutes after adherent cells are suspended. Finally, we find that optically stretched hMSCs exhibit power-law rheology during both loading and recovery; this evidence appears to be the first to originate from a biophysical measurement technique not involving cell-probe or cell-substratum contact. Together, these quantitative assessments of attached and suspended MSCs define the extremes of the extracellular environment while probing intracellular mechanisms that contribute to cell mechanical response.en_US
dc.description.sponsorshipArnold and Mabel Beckman Foundationen_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Career Grant CBET-0644846)en_US
dc.description.sponsorshipHuman Frontier Science Program (Strasbourg, France)en_US
dc.description.sponsorshipNational Institutes of Health. National Institute for Biomedical Imaging and Bioengineering (Grant EB006348)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.bpj.2010.08.052en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceElsevieren_US
dc.titleMesenchymal Stem Cell Mechanics from the Attached to the Suspended Stateen_US
dc.typeArticleen_US
dc.identifier.citationMaloney, John M., Dessy Nikova, Franziska Lautenschläger, Emer Clarke, Robert Langer, Jochen Guck, and Krystyn J. Van Vliet. “Mesenchymal Stem Cell Mechanics from the Attached to the Suspended State.” Biophysical Journal 99, no. 8 (October 2010): 2479–2487. © 2010 Biophysical Societyen_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.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.mitauthorMaloney, John M.en_US
dc.contributor.mitauthorNikova, Dessyen_US
dc.contributor.mitauthorVan Vliet, Krystyn J.en_US
dc.contributor.mitauthorLanger, Roberten_US
dc.relation.journalBiophysical Journalen_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.orderedauthorsMaloney, John M.; Nikova, Dessy; Lautenschläger, Franziska; Clarke, Emer; Langer, Robert; Guck, Jochen; Van Vliet, Krystyn J.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5735-0560
dc.identifier.orcidhttps://orcid.org/0000-0002-6853-811X
dc.identifier.orcidhttps://orcid.org/0000-0003-4255-0492
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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