Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2007-3-5
pubmed:abstractText
Reactive oxygen species (ROS) contribute to many glomerular diseases by targeting mesangial cells. ROS have been shown to regulate expression of many antioxidant enzymes including catalase. The mechanism by which the expression of catalase protein is regulated by ROS is not precisely known. Here we report that increased intracellular ROS level by hydrogen peroxide (H(2)O(2)) reduced the expression of catalase. H(2)O(2) increased phosphorylation of Akt kinase in a dose-dependent and sustained manner with a concomitant increase in the phosphorylation of FoxO1 transcription factor. Further analysis revealed that H(2)O(2) promoted rapid activation of phosphatidylinositol (PI) 3 kinase. The PI 3 kinase inhibitor Ly294002 and expression of tumor suppressor protein PTEN inhibited Akt kinase activity, resulting in the attenuation of FoxO1 phosphorylation and preventing the downregulating effect of H(2)O(2) on catalase protein level. Dominant negative Akt attenuated the inhibitory effect of H(2)O(2) on expression of catalase. Constitutively active FoxO1 increased the expression of catalase. However, dominant negative FoxO1 inhibited catalase protein level. Catalase transcription was reduced by H(2)O(2) treatment. Furthermore, expression of dominant negative Akt and constitutively active FoxO1 increased catalase transcription, respectively. These results demonstrate that ROS downregulate the expression of catalase in mesangial cells by PI 3 kinase/Akt signaling via FoxO1 as a target.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/2-(4-morpholinyl)-8-phenyl-4H-1-benz..., http://linkedlifedata.com/resource/pubmed/chemical/Catalase, http://linkedlifedata.com/resource/pubmed/chemical/Chromones, http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Forkhead Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Foxo1 protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/Hydrogen Peroxide, http://linkedlifedata.com/resource/pubmed/chemical/Morpholines, http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Oxidants, http://linkedlifedata.com/resource/pubmed/chemical/PTEN Phosphohydrolase, http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositol 3-Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-akt, http://linkedlifedata.com/resource/pubmed/chemical/Reactive Oxygen Species
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0021-9541
pubmed:author
pubmed:copyrightInfo
(c) 2007 Wiley-Liss, Inc.
pubmed:issnType
Print
pubmed:volume
211
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
457-67
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:17186497-Animals, pubmed-meshheading:17186497-Catalase, pubmed-meshheading:17186497-Cells, Cultured, pubmed-meshheading:17186497-Chromones, pubmed-meshheading:17186497-Dose-Response Relationship, Drug, pubmed-meshheading:17186497-Down-Regulation, pubmed-meshheading:17186497-Enzyme Activation, pubmed-meshheading:17186497-Enzyme Inhibitors, pubmed-meshheading:17186497-Forkhead Transcription Factors, pubmed-meshheading:17186497-Gene Expression Regulation, Enzymologic, pubmed-meshheading:17186497-Hydrogen Peroxide, pubmed-meshheading:17186497-Mesangial Cells, pubmed-meshheading:17186497-Morpholines, pubmed-meshheading:17186497-Nerve Tissue Proteins, pubmed-meshheading:17186497-Oxidants, pubmed-meshheading:17186497-PTEN Phosphohydrolase, pubmed-meshheading:17186497-Phosphatidylinositol 3-Kinases, pubmed-meshheading:17186497-Phosphorylation, pubmed-meshheading:17186497-Proto-Oncogene Proteins c-akt, pubmed-meshheading:17186497-Rats, pubmed-meshheading:17186497-Rats, Sprague-Dawley, pubmed-meshheading:17186497-Reactive Oxygen Species, pubmed-meshheading:17186497-Signal Transduction, pubmed-meshheading:17186497-Time Factors, pubmed-meshheading:17186497-Transfection
pubmed:year
2007
pubmed:articleTitle
Downregulation of catalase by reactive oxygen species via PI 3 kinase/Akt signaling in mesangial cells.
pubmed:affiliation
Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural