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Polymeric Osteopontin Employs Integrin alpha 9 beta 1 as a Receptor and Attracts Neutrophils by Presenting a de Novo Binding Site

https://hiroshima.repo.nii.ac.jp/records/2007228
https://hiroshima.repo.nii.ac.jp/records/2007228
2636ffb0-3d00-4f8b-a1db-cf134631b24d
名前 / ファイル ライセンス アクション
JBC_284_14769.pdf JBC_284_14769.pdf (829.4 KB)
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 Polymeric Osteopontin Employs Integrin alpha 9 beta 1 as a Receptor and Attracts Neutrophils by Presenting a de Novo Binding Site
言語 en
作成者 Nishimichi, Norihisa

× Nishimichi, Norihisa

en Nishimichi, Norihisa

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Higashikawa, Fumiko

× Higashikawa, Fumiko

en Higashikawa, Fumiko

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Kinoh, Hiromi H

× Kinoh, Hiromi H

en Kinoh, Hiromi H

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Tateishi, Yoshiko

× Tateishi, Yoshiko

en Tateishi, Yoshiko

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Matsuda, Haruo

× Matsuda, Haruo

en Matsuda, Haruo

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Yokosaki, Yasuyuki

× Yokosaki, Yasuyuki

en Yokosaki, Yasuyuki

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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
主題
主題Scheme NDC
主題 490
内容記述
内容記述 Osteopontin (OPN) is a cytokine and ligand for multiple members of the integrin family. OPN undergoes the in vivo polymerization catalyzed by cross-linking enzyme transglutaminase 2, which consequently increases the bioactivity through enhanced interaction with integrins. The integrin alpha 9 beta 1, highly expressed on neutrophils, binds to the sequence SVVYGLR only after intact OPN is cleaved by thrombin. The SVVYGLR sequence appears to be cryptic in intact OPN because alpha 9 beta 1 does not recognize intact OPN. Because transglutaminase 2-catalyzed polymers change their physical and chemical properties, we hypothesized that the SVVYGLR site might also be exposed on polymeric OPN. As expected, alpha 9 beta 1 turned into a receptor for polymeric OPN, a result obtained by cell adhesion and migration assays with alpha 9-transfected cells and by detection of direct binding of recombinant soluble alpha 9 beta 1 with colorimetry and surface plasmon resonance analysis. Because the N-terminal fragment of thrombincleaved OPN, a ligand for alpha 9 beta 1, has been reported to attract neutrophils, we next examined migration of neutrophils to polymeric OPN using time-lapse microscopy. Polymeric OPN showed potent neutrophil chemotactic activity, which was clearly inhibited by anti-alpha 9 beta 1 antibody. Unexpectedly, mutagenesis studies showed that alpha 9 beta 1 bound to polymeric OPN independently of the SVVYGLR sequence, and further, SVVYGLR sequence of polymeric OPN was cryptic because SVVYGLR-specific antibody did not recognize polymeric OPN. These results demonstrate that polymerization of OPN generates a novel alpha 9 beta 1-binding site and that the interaction of this site with the alpha 9 beta 1 integrin is critical to the neutrophil chemotaxis induced by polymeric OPN.
言語 en
出版者
出版者 Amer Soc Biochemistry Molecular Biology Iec
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 10.1074/jbc.M901515200
関連情報
識別子タイプ DOI
関連識別子 http://dx.doi.org/10.1074/jbc.M901515200
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0021-9258
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AA00251083
開始ページ
開始ページ 14769
書誌情報 Journal of Bioligical Chemistry
Journal of Bioligical Chemistry

巻 284, 号 22, p. 14769-14776, 発行日 2009
旧ID 27775
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