Human Mpv17-like protein is localized in peroxisomes and regulates expression of antioxidant enzymes (Q24319739)

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Toshihiro Yasuda

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Etsuko Tsubota

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Hisakazu Takatsuka

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Takasumi Matsuki

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Koichiro Kishi

Biochemical and Biophysical Research Communications

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language of work or name

English

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publication date

9 June 2006

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published in

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volume

344

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issue

3

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page(s)

948-54

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cites work

The glomerulosclerosis gene Mpv17 encodes a peroxisomal protein producing reactive oxygen species

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Cloning, mapping, genomic organization, and expression of mouse M-LP, a new member of the peroxisomal membrane protein Mpv17 domain family

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Inner ear defect similar to Alport's syndrome in the glomerulosclerosis mouse model Mpv17

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Endogenous hydrogen peroxide and peroxidative metabolism in adipocytes in response to insulin and sulfhydryl reagents

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Transgenic mouse model of kidney disease: Insertional inactivation of ubiquitously expressed gene leads to nephrotic syndrome

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A novel alternative spliced Mpv17-like protein isoform localizes in cytosol and is expressed in a kidney- and adult-specific manner

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Glomerular overproduction of oxygen radicals in Mpv17 gene-inactivated mice causes podocyte foot process flattening and proteinuria: A model of steroid-resistant nephrosis sensitive to radical scavenger therapy.

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The regulation of catalase gene expression in mouse muscle cells is dependent on the CCAAT-binding factor NF-Y.

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p38 Mitogen-activated protein kinase is a critical component of the redox-sensitive signaling pathways activated by angiotensin II. Role in vascular smooth muscle cell hypertrophy.

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M-LP, Mpv17-like protein, has a peroxisomal membrane targeting signal comprising a transmembrane domain and a positively charged loop and up-regulates expression of the manganese superoxide dismutase gene

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Production of hydrogen peroxide by transforming growth factor-beta 1 and its involvement in induction of egr-1 in mouse osteoblastic cells

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Prooxidant states and tumor promotion

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Enhanced gamma-glutamyl transpeptidase expression and superoxide production in Mpv17-/- glomerulosclerosis mice

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