Literature DB >> 9587138

Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis.

Z L Harris1, L W Klomp, J D Gitlin.   

Abstract

Aceruloplasminemia is an autosomal recessive disorder characterized by progressive neurodegeneration of the retina and basal ganglia associated with specific inherited mutations in the ceruloplasmin gene. Clinical and pathologic studies in patients with aceruloplasminemia revealed a marked accumulation of iron in affected parenchymal tissues, a finding consistent with early work identifying ceruloplasmin as a ferroxidase and with recent findings showing an essential role for a homologous copper oxidase in iron metabolism in yeast. The presence of neurologic symptoms in aceruloplasminemia is unique among the known inherited and acquired disorders of iron metabolism; recent studies revealed an essential role for astrocyte-specific expression of ceruloplasmin in iron metabolism and neuronal survival in the central nervous system. Recognition of aceruloplasminemia provides new insights into the genetic and environmental determinants of copper metabolism and has important implications for our understanding of the role of copper in human neurodegenerative diseases.

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Year:  1998        PMID: 9587138     DOI: 10.1093/ajcn/67.5.972S

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   7.045


  43 in total

1.  Mining copper transport genes.

Authors:  N C Andrews
Journal:  Proc Natl Acad Sci U S A       Date:  2001-06-05       Impact factor: 11.205

Review 2.  Iron homeostasis and eye disease.

Authors:  Allison Loh; Majda Hadziahmetovic; Joshua L Dunaief
Journal:  Biochim Biophys Acta       Date:  2008-11-14

Review 3.  Iron metabolism in the eye: a review.

Authors:  M Goralska; J Ferrell; J Harned; M Lall; S Nagar; L N Fleisher; M C McGahan
Journal:  Exp Eye Res       Date:  2008-11-21       Impact factor: 3.467

Review 4.  Aceruloplasminaemia: a rare but important cause of iron overload.

Authors:  Adam Doyle; Ferry Rusli; Prithi Bhathal
Journal:  BMJ Case Rep       Date:  2015-05-14

5.  Diagnosis of copper transport disorders.

Authors:  Lisbeth B Møller; Julia D Hicks; Courtney S Holmes; David S Goldstein; Cornelia Brendl; Peter Huppke; Stephen G Kaler
Journal:  Curr Protoc Hum Genet       Date:  2011-07

6.  Targeted suppression of the ferroxidase and iron trafficking activities of the multicopper oxidase Fet3p from Saccharomyces cerevisiae.

Authors:  Tzu-Pin Wang; Liliana Quintanar; Scott Severance; Edward I Solomon; Daniel J Kosman
Journal:  J Biol Inorg Chem       Date:  2003-04-09       Impact factor: 3.358

7.  Menkes Copper ATPase (Atp7a) is a novel metal-responsive gene in rat duodenum, and immunoreactive protein is present on brush-border and basolateral membrane domains.

Authors:  Jennifer J Ravia; Renu M Stephen; Fayez K Ghishan; James F Collins
Journal:  J Biol Chem       Date:  2005-08-04       Impact factor: 5.157

Review 8.  Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.

Authors:  P de Bie; P Muller; C Wijmenga; L W J Klomp
Journal:  J Med Genet       Date:  2007-08-23       Impact factor: 6.318

Review 9.  The SLC40 basolateral iron transporter family (IREG1/ferroportin/MTP1).

Authors:  Andrew T McKie; David J Barlow
Journal:  Pflugers Arch       Date:  2003-06-27       Impact factor: 3.657

10.  Copper binding components of blood plasma and organs, and their responses to influx of large doses of (65)Cu, in the mouse.

Authors:  Anthony Cabrera; Erin Alonzo; Eric Sauble; Yu Ling Chu; Dionne Nguyen; Maria C Linder; Dee S Sato; Andrew Z Mason
Journal:  Biometals       Date:  2008-03-21       Impact factor: 2.949

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