File | |
Title |
Suppressive effect of epigallocatechin-3-gallate, a constituent of green tea, on platelet-derived growth factor-BB signaling pathway in rat A7r5 cells
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Creator | |
Source Title |
Shimane journal of medical science
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Volume | 22 |
Issue | 1 |
Start Page | 1 |
End Page | 6 |
Journal Identifire |
ISSN 03865959
EISSN 24332410
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Descriptions |
Epigallocatechin-3-gallate (EGCG), a polyphenol constituent of popular beverage green tea, has been recently attracted much attention for the prevention of atherosclerosis, which is a systemic vessel disease and may lead to a variety of diseases including cardiovascular disease. Platelet-derived growth factor (PDGF) plays an important role as cell-proliferating factor in the pathogenic course of atherosclerosis, and increased activity in the PDGF signaling pathway has been implicated as a contributing factor in the progression. In the present study, to elucidate how EGCG affects the PDGF signaling pathway, we investigated the effect of EGCG on the PDGF-BBinduced activation of Ras-MAPK (mitogen-activated protein kinase) pathway, expression of immediateearly genes, and cell proliferation in rat A7r5 cells. EGCG significantly decreased PDGF-BB-induced ERK1/2 (extracellular signal-regulated kinase 1/2) and MEK1 (MAPK/ERK kinase 1) phosphorylation states dose-dependently, and also inhibited PDGFBB-induced c-fos and c-jun mRNA expressions and cell proliferation. Furthermore, PDGF-BB-induced tyrosine phosphorylation of the cognate receptor was significantly suppressed by EGCG, indicating that EGCG may act at and/or downstream the PDGF β-receptor. These results suggest that EGCG may suppress the cell proliferative signaling pathway through the inhibition of PDGF receptor kinase, MEK/ERK activity and immediate-early gene expressions. Thus, the habitual drinking of green tea may be useful to prevent atherosclerosis, and consequently decrease the mortality of cardiovascular diseases.
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Language |
eng
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Resource Type | departmental bulletin paper |
Publisher |
Shimane University Faculty of Medicine
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Date of Issued | 2005-03-01 |
Publish Type | Version of Record |
Access Rights | open access |
Relation |
[NCID] AA00841586
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Remark | http://ci.nii.ac.jp/vol_issue/nels/AA00841586_jp.html |