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Basic Fibroblast Growth Factor Induces The Expression of Matrix Metalloproteinase-3 in Human Periodontal Ligament Cells Through the MEK2 Mitogen-Activated Protein Kinase Pathway

https://hiroshima.repo.nii.ac.jp/records/2007460
https://hiroshima.repo.nii.ac.jp/records/2007460
bfb5dbcc-cc55-4e12-9a07-3ade62e9a44e
名前 / ファイル ライセンス アクション
JPR_38_122.pdf JPR_38_122.pdf (1.4 MB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル Basic Fibroblast Growth Factor Induces The Expression of Matrix Metalloproteinase-3 in Human Periodontal Ligament Cells Through the MEK2 Mitogen-Activated Protein Kinase Pathway
言語 en
作成者 Shimazu, Atsushi

× Shimazu, Atsushi

en Shimazu, Atsushi

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Morishita, Masayuki

× Morishita, Masayuki

en Morishita, Masayuki

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
権利情報 Copyright (c) 2003 Blackwell Publishing. The definitive version is available at www.blackwell-synergy.com
主題
主題Scheme Other
主題 periodontal ligament (PDL)
主題
主題Scheme Other
主題 basic fibroblast growth factor (bFGF, FGF-2)
主題
主題Scheme Other
主題 matrix metalloproteinase (MMP) -3
主題
主題Scheme Other
主題 mitogen-activated protein (MAP) kinase
主題
主題Scheme NDC
主題 490
内容記述
内容記述 Basic fibroblast growth factor (bFGF, FGF-2) is one of the potent mitogens for periodontal ligament (PDL) cells. However, the role of bFGF on the matrix metalloproteinase-3 (MMP-3) expression in PDL cells is unknown. In this study, the effect of bFGF on MMP-3 expression in PDL cells and the mechanism of this process were examined. Human PDL cells were exposed to bFGF at various concentrations (0.01–10 ng/ml) in monolayer cultures. bFGF increased [3H]thymidine incorporation and suppressed proteoglycan synthesis concentration-dependently. However, similar concentration ranges of bFGF increased the release of the cell-associated proteoglycans into the medium. Furthermore, bFGF increased MMP-3 mRNA levels concentration-dependently as examined by reverse transcription-polymerase chain reaction (RT-PCR). Induction of MMP-3 after the stimulation with bFGF was observed as early as 12 h with maximal at 24 h. Thereafter, the MMP-3 mRNA level gradually decreased until 72 h. Cycloheximide blocked the induction of MMP-3 by bFGF, indicating the requirement of de novo protein synthesis for this stimulation. Furthermore, MMP-3 expression induced by bFGF was abrogated by U0126, a specific inhibitor of MEK1/2 and ERK1/2 in mitogen-activated protein (MAP) kinase pathway, not by PD98059, a specific inhibitor of MEK1. In addition, bFGF up-regulated the phosphorylated ERK1/2 in 5 min with the maximal at 20 min as examined by Western blotting, and U0126 inhibited the ERK1/2 phosphorylation induced by bFGF. These findings suggest that bFGF induces MMP-3 expression in PDL cells through the activation of the MEK2 in MAP kinase pathway. bFGF stimulation on MMP-3 synthesis may be involved in the control of the cell-associated proteoglycans in PDL cells during periodontal regeneration and degradation.
言語 en
出版者
出版者 Blackwell
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版タイプ
出版タイプ AO
出版タイプResource http://purl.org/coar/version/c_b1a7d7d4d402bcce
関連情報
識別子タイプ DOI
関連識別子 10.1034/j.1600-0765.2003.01645.x
関連情報
識別子タイプ DOI
関連識別子 http://dx.doi.org/10.1034/j.1600-0765.2003.01645.x
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0022-3484
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AA00704381
開始ページ
開始ページ 122
書誌情報 Journal of Periodontal Research
Journal of Periodontal Research

巻 38, 号 2, p. 122-129, 発行日 2003
旧ID 21547
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