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The influence of extra-cellular matrix and stroma remodeling on the productivity of long-term human bone marrow cultures

dc.contributor.authorSchwartz, Richard M.en_US
dc.contributor.authorCaldwell, Jerryen_US
dc.contributor.authorClarke, Michael F.en_US
dc.contributor.authorEmerson, Stephen G.en_US
dc.contributor.authorPalsson, Bernhard Øen_US
dc.date.accessioned2006-09-08T20:31:52Z
dc.date.available2006-09-08T20:31:52Z
dc.date.issued1992-01en_US
dc.identifier.citationSchwartz, Richard M.; Caldwell, Jerry; Clarke, Michael F.; Emerson, Stephen G.; Palsson, Bernhard Ø; (1992). "The influence of extra-cellular matrix and stroma remodeling on the productivity of long-term human bone marrow cultures." Cytotechnology 10(3): 217-224. <http://hdl.handle.net/2027.42/42613>en_US
dc.identifier.issn0920-9069en_US
dc.identifier.issn1573-0778en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42613
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1369237&dopt=citationen_US
dc.description.abstractThe stromal cell layer is believed to play an important role in long-term human bone marrow cultures (LTHBMCs). At present, neither the role that the stromal cell extra-cellular matrix (ECM) plays in influencing stroma behavior is well understood nor are the effects of stroma aging. Rapid medium exchanged LTHBMCs were established on surfaces precoated with human natural fibronectin and type 1 rat tail collagen. Although initial adhesion of hematopoietic cells was improved by the presence of both ECMs, the overall progenitor and nonadherent cell productivity was not improved nor did the stroma grow to confluency faster. Thus, the ECMs used did not significantly influence the cell productivity of LTHBMCs. To examine the influence of stromal cell layer aging, conditioned medium was obtained from the first two weeks of LTHBMCs that was subsequently concentrated and used as a medium supplement in a second set of slowly exchanged LTHBMCs. The presence of the concentrated conditioned medium (conCM) enhanced the production of nonadherent cells three-fold compared with control over an eight week culture period. Control cultures that were exposed to conCM after 4 weeks in culture significantly improved their cell productivity during the latter 4 weeks of culture compared with control. The productivity of cultures exposed to conCM for 4 weeks dropped significantly when unsupplemented medium was used for the latter 4 weeks of culture. Interestingly, phytohemagglutin-stimulated leukocyte-conditioned medium stimulated LTHMBCs in a similar fashion, as did conditioned medium from early LTHBMCs. Taken together, these results strongly suggest that the stromal cell layer does produce important factors for active hematopoiesis during its growth to confluence.en_US
dc.format.extent657887 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Springer Science+Business Mediaen_US
dc.subject.otherLife Sciencesen_US
dc.subject.otherAnimal Anatomy / Morphology / Histologyen_US
dc.subject.otherHematopoiesisen_US
dc.subject.otherExtra-cellular Matrixen_US
dc.subject.otherStromal Cellsen_US
dc.subject.otherConditioned Mediumen_US
dc.subject.otherRapid Perfusionen_US
dc.titleThe influence of extra-cellular matrix and stroma remodeling on the productivity of long-term human bone marrow culturesen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumCellular Biotechnology Laboratory, Department of Chemical Engineering, University of Michigan, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumCellular Biotechnology Laboratory, Department of Chemical Engineering, University of Michigan, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDivision of Hematology and Oncology, Department of Internal Medicine, University of Michigan, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDivision of Hematology and Oncology, Department of Internal Medicine, University of Michigan, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumCellular Biotechnology Laboratory, Department of Chemical Engineering, University of Michigan, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid1369237en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42613/1/10616_2004_Article_BF00146672.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00146672en_US
dc.identifier.sourceCytotechnologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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