Literature DB >> 9833325

Analysis of the distribution of Cu, Fe and Zn and other elements in brindled mouse kidney using a scanning proton microprobe.

B J Kirby1, D M Danks, G J Legge, J F Mercer.   

Abstract

An analysis of the distribution of trace metals in the kidney cortex in normal and brindled male mice has been carried out with a scanning proton microprobe. Enzyme histochemical staining techniques were used to distinguish between proximal and distal tubules. Average copper levels were increased in brindled kidney tissue sections, with the above-normal Cu accumulation found to occur entirely within the proximal tubules. Therefore, the proximal tubule is now regarded as the location where the defect in Cu transport in brindled mice is manifested the most clearly. The distribution of Fe was found to be non-uniform with some tubule cross-sections exhibiting high concentrations in both genotypes. The distribution of Zn was found to be uniform, and the concentration was similar for each genotype.

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Year:  1998        PMID: 9833325     DOI: 10.1016/s0162-0134(98)10053-3

Source DB:  PubMed          Journal:  J Inorg Biochem        ISSN: 0162-0134            Impact factor:   4.155


  7 in total

1.  Pathological structure of the kidney from adult mice with mosaic mutation.

Authors:  M Lenartowicz; M Kowal; D Buda-Lewandowska; J Styrna
Journal:  J Inherit Metab Dis       Date:  2002-12       Impact factor: 4.982

Review 2.  In situ imaging of metals in cells and tissues.

Authors:  Reagan McRae; Pritha Bagchi; S Sumalekshmy; Christoph J Fahrni
Journal:  Chem Rev       Date:  2009-10       Impact factor: 60.622

3.  Cell-specific trafficking suggests a new role for renal ATP7B in the intracellular copper storage.

Authors:  Natalie Barnes; Mee Y Bartee; Lita Braiterman; Arnab Gupta; Vladimir Ustiyan; Vesna Zuzel; Jack H Kaplan; Ann L Hubbard; Svetlana Lutsenko
Journal:  Traffic       Date:  2009-02-18       Impact factor: 6.215

4.  Prenatal treatment of mosaic mice (Atp7a mo-ms) mouse model for Menkes disease, with copper combined by dimethyldithiocarbamate (DMDTC).

Authors:  Małgorzata Lenartowicz; Wojciech Krzeptowski; Paweł Koteja; Katarzyna Chrząścik; Lisbeth Birk Møller
Journal:  PLoS One       Date:  2012-07-18       Impact factor: 3.240

5.  Decreased Expression of the Slc31a1 Gene and Cytoplasmic Relocalization of Membrane CTR1 Protein in Renal Epithelial Cells: A Potent Protective Mechanism against Copper Nephrotoxicity in a Mouse Model of Menkes Disease.

Authors:  Olga Haberkiewicz; Paweł Lipiński; Rafał R Starzyński; Aneta Jończy; Patrycja Kurowska; Mateusz Ogórek; Aleksandra Bednarz; Sylwia Herman; Dawid Hatala; Paweł Grzmil; Zenon Rajfur; Zbigniew Baster; Małgorzata Lenartowicz
Journal:  Int J Mol Sci       Date:  2022-09-28       Impact factor: 6.208

6.  Haemolysis and perturbations in the systemic iron metabolism of suckling, copper-deficient mosaic mutant mice - an animal model of Menkes disease.

Authors:  Małgorzata Lenartowicz; Rafał R Starzyński; Wojciech Krzeptowski; Paweł Grzmil; Aleksandra Bednarz; Mateusz Ogórek; Olga Pierzchała; Robert Staroń; Anna Gajowiak; Paweł Lipiński
Journal:  PLoS One       Date:  2014-09-23       Impact factor: 3.240

Review 7.  Mottled Mice and Non-Mammalian Models of Menkes Disease.

Authors:  Małgorzata Lenartowicz; Wojciech Krzeptowski; Paweł Lipiński; Paweł Grzmil; Rafał Starzyński; Olga Pierzchała; Lisbeth Birk Møller
Journal:  Front Mol Neurosci       Date:  2015-12-18       Impact factor: 5.639

  7 in total

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