Source:http://linkedlifedata.com/resource/pubmed/id/17942966
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2007-10-26
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pubmed:abstractText |
Mice deficient in either platelet-derived growth factor (PDGF) B chain or PDGF receptor (PDGFR) beta lack mesangial cells. PDGF stimulates proliferation and migration of metanephric mesenchymal cells, from which mesangial cells are derived. Binding of PDGF to PDGFR-beta induces autophosphorylation at specific tyrosine residues and activates various effector proteins, including phosphatidylinositol-3-kinase (PI3-K). This study explored the role of PI 3-K and reactive oxygen species (ROS) in PDGF-mediated signaling using cells established from wild-type and PDGFR-beta -/- metanephric blastemas at 11.5 days post-conception. PDGF-induced effects that were dependent on PI3-K activation were determined using PDGFR-beta -/- cells made to express "add-back" mutant PDGFR-beta capable of binding PI3-K. We found that PDGF is mitogenic for mesenchymal cells expressing PDGFR-beta, and PI3-K is an important regulator of PDGF-induced DNA synthesis. Activation of ERK1/2 is partially dependent on PI3-K, and both the PI3-K and MEK-ERK1/2 pathways contribute to PI3-K-dependent mitogenesis. In addition, PDGF-induced DNA synthesis in wild-type cells was found to be dependent on ROS that are generated downstream of PI3-K activation. Using antisense oligonucleotides and small interfering RNA, we determined that the NAD(P)H oxidase Nox4 produces these ROS that activate Akt and the MEK-ERK1/2 mitogenic cascade. In conclusion, the present study demonstrates Nox4 involvement in PDGF-induced DNA synthesis in metanephric mesenchymal cells and provides the first evidence that PDGF-induced PI3-K activity enhances production of ROS by Nox4.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/NADPH Oxidase,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositol 3-Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Platelet-Derived Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Reactive Oxygen Species,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Platelet-Derived Growth...
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1533-3450
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2903-11
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:17942966-Animals,
pubmed-meshheading:17942966-Cell Culture Techniques,
pubmed-meshheading:17942966-Kidney Glomerulus,
pubmed-meshheading:17942966-Mesoderm,
pubmed-meshheading:17942966-Mice,
pubmed-meshheading:17942966-Mitosis,
pubmed-meshheading:17942966-NADPH Oxidase,
pubmed-meshheading:17942966-Phosphatidylinositol 3-Kinases,
pubmed-meshheading:17942966-Platelet-Derived Growth Factor,
pubmed-meshheading:17942966-Reactive Oxygen Species,
pubmed-meshheading:17942966-Receptor, Platelet-Derived Growth Factor beta,
pubmed-meshheading:17942966-Signal Transduction
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pubmed:year |
2007
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pubmed:articleTitle |
Mitogenic signaling via platelet-derived growth factor beta in metanephric mesenchymal cells.
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pubmed:affiliation |
Division of Nephrology, Department of Medicine, University of Texas Health Science Center, San Antonio, Texas 78229-3900, USA. wagnerb@uthscsa.edu
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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
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