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Regulation of rat mammary gene expression by extracellular matrix components

dc.contributor.authorBlum, Joanne L.en_US
dc.contributor.authorZeigler, Mary E.en_US
dc.contributor.authorWicha, Max S.en_US
dc.date.accessioned2006-04-07T19:45:07Z
dc.date.available2006-04-07T19:45:07Z
dc.date.issued1987-12en_US
dc.identifier.citationBlum, Joanne L., Zeigler, Mary E., Wicha, Max S. (1987/12)."Regulation of rat mammary gene expression by extracellular matrix components." Experimental Cell Research 173(2): 322-340. <http://hdl.handle.net/2027.42/26485>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WFC-4DTSSV3-4P/2/e1aab6e8a66fbb1cf59b6676c5d68ae6en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/26485
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3691666&dopt=citationen_US
dc.description.abstractIn the mammary gland the induction and maintenance of differentiation are dependent on both lactogenic hormones and the extracellular matrix (ECM). Since mammary epithelial cells differentiate on a basement membrane in vivo we have examined the effects of basement membrane components on the expression of milk protein genes in primary rat mammary cultures. We examined the effects of a basement membrane gel derived from the Englebreth-Holm-Swarm tumor as well as its major component, laminin, on the expression of a group of milk protein genes. We demonstrate that the basement membrane gel induces [alpha]-casein and [alpha]-lactalbumin ([alpha]-LA) accumulation up to 160- and 70-fold, respectively, of that on tissue culture plastic. Laminin, a major component of the basement membrane, also caused significant induction of these same proteins. In order to determine whether these ECM effects occurred at a translational or post-translational level, pulse-chase experiments were performed. These experiments demonstrated that a laminin substratum selectively effects milk protein turnover and secretion. In order to demonstrate whether ECM effects occurred at the level of steady state accumulation of mRNA we performed dot blot and Northern analyses using cloned cDNA probes for [alpha]-, [beta]-, and [gamma]-caseins and [alpha]-LA. These studies demonstrated that ECM components induced [alpha]- and [beta]-caseins up to 10-fold and [alpha]-LA up to 3-fold, with no significant effect on [gamma]-casein. These results demonstrate that milk protein genes are not coordinately regulated by ECM components. Furthermore, since the amount of induction of milk proteins exceeds the amount of induction of mRNAs for these proteins, we conclude that in our system a major effect of ECM components is at the translational and/or post-translational levels. Based on these findings we propose a model in which basement membrane components effect mammary gene expression at multiple levels.en_US
dc.format.extent5340964 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleRegulation of rat mammary gene expression by extracellular matrix componentsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_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.affiliationumDivision of Hematology/Oncology, Department of Internal Medicine and Program in Cell and Molecular Biology, Simpson Memorial Research Institute, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.contributor.affiliationumDivision of Hematology/Oncology, Department of Internal Medicine and Program in Cell and Molecular Biology, Simpson Memorial Research Institute, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.contributor.affiliationumDivision of Hematology/Oncology, Department of Internal Medicine and Program in Cell and Molecular Biology, Simpson Memorial Research Institute, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.identifier.pmid3691666en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/26485/1/0000021.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0014-4827(87)90274-6en_US
dc.identifier.sourceExperimental Cell Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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