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Observations consistent with autocrine stimulation of hybridoma cell growth and implications for large-scale antibody production

dc.contributor.authorLee, Gyun Minen_US
dc.contributor.authorKaminski, Mark S.en_US
dc.contributor.authorPalsson, Bernhard Øen_US
dc.date.accessioned2006-09-08T20:12:32Z
dc.date.available2006-09-08T20:12:32Z
dc.date.issued1992-04en_US
dc.identifier.citationLee, Gyun Min; Kaminski, Mark S.; Palsson, Bernhard O.; (1992). "Observations consistent with autocrine stimulation of hybridoma cell growth and implications for large-scale antibody production." Biotechnology Letters 14(4): 257-262. <http://hdl.handle.net/2027.42/42316>en_US
dc.identifier.issn0141-5492en_US
dc.identifier.issn1573-6776en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42316
dc.description.abstractExistence of autocrine growth factors (aGFs) may influence the serum requirement for growth of hybridoma cells and thus significantly influence process economics. For the murine hybridoma cell line S3H5/γ2bA2, critical inoculum density (cID) and serum requirement for growth were inversely related for cultivation in both T flasks and spinner flasks. In spinner flasks, an inoculum density of 10 6 cells/ml was necessary for the cells to grow in RPMI 1640 medium without serum supplement, and an inoculum density of 10 3 cell/ml was necessary in RPMI 1640 medium with 10% serum. In T flasks, where the local cell density is higher than in spinner flasks, an inoculum density of 10 6 cells/ml was necessary for the cells to grow in RPMI 1640 medium without serum supplement, and an inoculum density of 1 cell/ml was also necessary in RPMI 1640 medium with 10% serum. Further, immobilized cells at high local cell density could grow under conditions where cells in T flasks at corresponding overall cell density could not grow. The cells at high inoculum density were less sensitive to shear induced by mechanical agitation than the cells at low inoculum density. Taken together these observations support the existence of secreted aGF(s) by the hybridoma cell line used. Since the specific MAb production rate was independent of cultivation method and inoculum density, the existence of autocrine growth factors would suggest that the use of immobilized cells should improve the economics of MAb production.en_US
dc.format.extent764640 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.otherChemistryen_US
dc.subject.otherBiotechnologyen_US
dc.subject.otherOrganic Chemistryen_US
dc.subject.otherBioorganic Chemistryen_US
dc.subject.otherBiochemistry, Generalen_US
dc.subject.otherMicrobiologyen_US
dc.subject.otherAnimal Anatomy / Morphology / Histologyen_US
dc.titleObservations consistent with autocrine stimulation of hybridoma cell growth and implications for large-scale antibody productionen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumCellular Biotechnology Laboratory, Department of Chemical Engineering, University of Michigan, Herbert H. Dow Building, 48109, Ann Arbor, MIen_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan, Herbert H. Dow Building, 48109, Ann Arbor, MIen_US
dc.contributor.affiliationumCellular Biotechnology Laboratory, Department of Chemical Engineering, University of Michigan, Herbert H. Dow Building, 48109, Ann Arbor, MIen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42316/1/10529_2005_Article_BF01022320.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01022320en_US
dc.identifier.sourceBiotechnology Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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