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A cone-plate apparatus for the in vitro biochemical and molecular analysis of the effect of shear stress on adherent cells

dc.contributor.authorMalek, Adel M.en_US
dc.contributor.authorAhlquist, Richarden_US
dc.contributor.authorGibbons, Gary H.en_US
dc.contributor.authorDzau, Victor J.en_US
dc.contributor.authorIzumo, Seigoen_US
dc.date.accessioned2006-09-08T21:12:58Z
dc.date.available2006-09-08T21:12:58Z
dc.date.issued1995-09en_US
dc.identifier.citationMalek, Adel M.; Ahlquist, Richard; Gibbons, Gary H.; Dzau, Victor J.; Izumo, Seigo; (1995). "A cone-plate apparatus for the in vitro biochemical and molecular analysis of the effect of shear stress on adherent cells." Methods in Cell Science 17(3): 165-176. <http://hdl.handle.net/2027.42/43234>en_US
dc.identifier.issn1381-5741en_US
dc.identifier.issn1573-0603en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/43234
dc.description.abstractLiving cells are constantly exposed to a variety of complex mechanical stimuli which are though to be critical in the control of tissue structure and function. Endothelial and smooth muscle cells in the blood vessel are ideal candidates for the study of blood flow-induced cellular regulation. We describe here a cone-plate viscometer apparatus which is specially-designed for studying the effect of fluid shear stress on large populations of adherent cells in vitro. Using conventional polystyrene tissue culture plates, the apparatus is self-contained, fits inside a standard tissue culture incubator, and provides 75–150 cm 2 of useful surface area for cell growth. This capability makes it ideal for studying gene regulation using Northern analysis, nuclear runoff transcription, transfection with reporter constructs, as well as immunochemical staining. The closed-volume design of the device is also well-suited for isotopic labelling, pharmacological studies, and for the detection of minute amounts of secreted cell products. The setup allows the use of either steady, time- and direction-varying laminar, or turbulent shear stress. We provide a detailed assembly procedure and review the method for computing shear stress magnitude and Reynolds number. Ink flow analysis, dynamic response characterization, and LDH measurements are presented to confirm the device's fluid mechanical properties and demonstrate the absence of cell injury.en_US
dc.format.extent1722121 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 Biochemistryen_US
dc.subject.otherPlant Sciencesen_US
dc.subject.otherAnimal Anatomy / Morphology / Histologyen_US
dc.subject.otherBiomechanicsen_US
dc.subject.otherCell Cultureen_US
dc.subject.otherEndotheliumen_US
dc.subject.otherMechanotransductionen_US
dc.subject.otherMechanical Stressen_US
dc.subject.otherScientific Instrumentsen_US
dc.subject.otherRheologyen_US
dc.titleA cone-plate apparatus for the in vitro biochemical and molecular analysis of the effect of shear stress on adherent cellsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumCardiovascular Research Center, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherDepartment of Neurosurgery, Brigham & Women's Hospital/Children's Hospital and Harvard Medical School, Boston, MAen_US
dc.contributor.affiliationotherDepartment of Neurosurgery, Brigham & Women's Hospital/Children's Hospital and Harvard Medical School, Boston, MAen_US
dc.contributor.affiliationotherFalk Cardiovascular Center, Stanford University Medical School, Stanford, CAen_US
dc.contributor.affiliationotherFalk Cardiovascular Center, Stanford University Medical School, Stanford, CAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/43234/1/11022_2004_Article_BF00996123.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00996123en_US
dc.identifier.sourceMethods in Cell Scienceen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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