Article: ZIP2 and ZIP4 mediate age-related zinc fluxes across the retinal pigment epithelium

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TitleZIP2 and ZIP4 mediate age-related zinc fluxes across the retinal pigment epithelium
AuthorsLeung, KW1
Gvritishvili, A1
Liu, Y1
TombranTink, J1
KeywordsAge-related macular degeneration
Aging
Retina
RPE cells
Zinc transport
Zinc transporters
Issue Date2012
CitationJournal Of Molecular Neuroscience, 2012, v. 46 n. 2, p. 122-137 [How to Cite?]
DOI: http://dx.doi.org/10.1007/s12031-011-9536-0
AbstractDecreases in systemic and cellular levels of zinc (Zn 2+) during normal aging correlate with several age-related pathologies including age-related macular degeneration. Zn 2+ homeostasis in tissues is not only dependent on dietary intake but also on optimal expression and function of its influx (ZIP) and efflux (ZnT) transporters. We recently showed that many of the Zn 2+ transporters are expressed by the retinal pigment epithelial (RPE) cells. In this study, we present evidence that RPE cells contain less endogenous Zn 2+ with increased aging and transport this ion vectorially with greater transport from the basal to apical direction. Expression of two Zn 2+ influx transporters, ZIP2 and ZIP4, is reduced as a function of RPE age. Gene silencing of ZIP2 and ZIP4 in RPE cells from young donors or their overexpression in cells from older donors confirms that these two transporters are essential in controlling Zn 2+ influx and sequestration in RPE cells. Both transporters are distributed on the basal surface of the RPE where they are likely to control Zn 2+ homeostasis in the outer retina. © Springer Science+Business Media, LLC 2011.
ISSN0895-8696
2011 Impact Factor: 2.504
2011 SCImago Journal Rankings: 0.221
DOIhttp://dx.doi.org/10.1007/s12031-011-9536-0
ReferencesReferences in Scopus
DC Field
Value
dc.contributor.authorLeung, KW
dc.contributor.authorGvritishvili, A
dc.contributor.authorLiu, Y
dc.contributor.authorTombranTink, J
dc.date.accessioned2012-10-25T04:57:11Z
dc.date.available2012-10-25T04:57:11Z
dc.date.issued2012
dc.description.abstractDecreases in systemic and cellular levels of zinc (Zn 2+) during normal aging correlate with several age-related pathologies including age-related macular degeneration. Zn 2+ homeostasis in tissues is not only dependent on dietary intake but also on optimal expression and function of its influx (ZIP) and efflux (ZnT) transporters. We recently showed that many of the Zn 2+ transporters are expressed by the retinal pigment epithelial (RPE) cells. In this study, we present evidence that RPE cells contain less endogenous Zn 2+ with increased aging and transport this ion vectorially with greater transport from the basal to apical direction. Expression of two Zn 2+ influx transporters, ZIP2 and ZIP4, is reduced as a function of RPE age. Gene silencing of ZIP2 and ZIP4 in RPE cells from young donors or their overexpression in cells from older donors confirms that these two transporters are essential in controlling Zn 2+ influx and sequestration in RPE cells. Both transporters are distributed on the basal surface of the RPE where they are likely to control Zn 2+ homeostasis in the outer retina. © Springer Science+Business Media, LLC 2011.
dc.description.natureLink_to_subscribed_fulltext
dc.identifier.citationJournal Of Molecular Neuroscience, 2012, v. 46 n. 2, p. 122-137 [How to Cite?]
DOI: http://dx.doi.org/10.1007/s12031-011-9536-0
dc.identifier.citeulike9363874
dc.identifier.doihttp://dx.doi.org/10.1007/s12031-011-9536-0
dc.identifier.epage137
dc.identifier.issn0895-8696
2011 Impact Factor: 2.504
2011 SCImago Journal Rankings: 0.221
dc.identifier.issue2
dc.identifier.scopuseid_2-s2.0-84863385420
dc.identifier.spage122
dc.identifier.urihttp://hdl.handle.net/10722/169868
dc.identifier.volume46
dc.languageeng
dc.publisher.placeUnited States
dc.relation.ispartofJournal of Molecular Neuroscience
dc.relation.referencesReferences in Scopus
dc.subjectAge-related macular degeneration
dc.subjectAging
dc.subjectRetina
dc.subjectRPE cells
dc.subjectZinc transport
dc.subjectZinc transporters
dc.titleZIP2 and ZIP4 mediate age-related zinc fluxes across the retinal pigment epithelium
dc.typeArticle
Author Affiliations
  1. Penn State College of Medicine