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pubmed-article:10733933pubmed:abstractTextCaco-2 cells undergo differentiation to an enterocytic-like cell when maintained in a post-confluent state for 1-2 weeks. During this period Caco-2 cells begin to express high levels brush border membrane associated enzymes such as dipeptidyl peptidase IV. Using the dipeptidyl peptidase IV gene promoter in electrophoretic mobility shift assays, we have shown for the first time that levels of hepatocyte nuclear factor 1alpha increase three- to fourfold during Caco-2 cell differentiation. Transient cotransfection experiments with 3T3 cells using dipeptidyl peptidase IV promoter constructs and expression vectors containing hepatocyte nuclear factor 1alpha and beta show that the ratio of alpha and beta modulates reporter gene expression. These results suggest that the increase in levels of hepatocyte nuclear factor 1alpha that occur during intestinal cell differentiation, are important for expression of dipeptidyl peptidase IV and other intestinal proteins.lld:pubmed
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pubmed-article:10733933pubmed:authorpubmed-author:KimY SYSlld:pubmed
pubmed-article:10733933pubmed:authorpubmed-author:EricksonR HRHlld:pubmed
pubmed-article:10733933pubmed:authorpubmed-author:LamR WRWlld:pubmed
pubmed-article:10733933pubmed:copyrightInfoCopyright 2000 Academic Press.lld:pubmed
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pubmed-article:10733933pubmed:pagination235-9lld:pubmed
pubmed-article:10733933pubmed:dateRevised2010-11-18lld:pubmed
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pubmed-article:10733933pubmed:articleTitleRole of hepatocyte nuclear factor 1alpha and 1beta in the transcriptional regulation of human dipeptidyl peptidase IV during differentiation of Caco-2 cells.lld:pubmed
pubmed-article:10733933pubmed:affiliationGastrointestinal Research Laboratory, Department of Veterans Affairs Medical Center, San Francisco, California 94121, USA. neko@itsa.ucsf.edulld:pubmed
pubmed-article:10733933pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10733933pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:10733933pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
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