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Authordc.contributor.authorEspinoza, Alejandra 
Authordc.contributor.authorLe Blanc, Solange 
Authordc.contributor.authorOlivares, Manuel 
Authordc.contributor.authorPizarro Aguirre, Fernando 
Authordc.contributor.authorRuz, Manuel 
Authordc.contributor.authorArredondo, Miguel 
Admission datedc.date.accessioned2019-03-11T13:04:02Z
Available datedc.date.available2019-03-11T13:04:02Z
Publication datedc.date.issued2012
Cita de ítemdc.identifier.citationBiological Trace Element Research, Volumen 146, Issue 2, 2018, Pages 281-286
Identifierdc.identifier.issn01634984
Identifierdc.identifier.issn15590720
Identifierdc.identifier.other10.1007/s12011-011-9243-2
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/165593
Abstractdc.description.abstractIron (Fe), copper (Cu), and zinc (Zn) fulfill various essential biological functions and are vital for all living organisms. They play important roles in oxygen transport, cell growth and differentiation, neurotransmitter synthesis, myelination, and synaptic transmission. Because of their role in many critical functions, they are commonly used in food fortification and supplementation strategies globally. To determine the involvement of divalent metal transporter 1 (DMT1) and human copper transporter 1 (hCTR1) on Fe, Cu, and Zn uptake, Caco-2 cells were transfected with four different shRNA plasmids to selectively inhibit DMT1 or hCTR1 transporter expression. Fe and Cu uptake and total Zn content measurements were performed in shRNA-DMT1 and shRNA-hCTR1 cells. Both shRNA-DMT1 and shRNA-hCTR1 cells had lower apical Fe uptake (a decrease of 51% and 41%, respectively), Cu uptake (a decrease of 25.8% and 38.5%, respectively), and Zn content (a decrease of 23.1% and 22.7%, respectively) com
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceBiological Trace Element Research
Keywordsdc.subjectCopper
Keywordsdc.subjectDMT1
Keywordsdc.subjectHCTR1
Keywordsdc.subjectIron
Keywordsdc.subjectShRNA
Keywordsdc.subjectZinc
Títulodc.titleIron, copper, and zinc transport: Inhibition of divalent metal transporter 1 (DMT1) and human copper transporter 1 (hCTR1) by shRNA
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile