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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 1. 査読済論文(医学・保健)

Ligand-independent Tie2 dimers mediate kinase activity stimulated by high dose angiopoietin-1

https://doi.org/10.24517/00062983
https://doi.org/10.24517/00062983
114009d0-e706-476b-b399-253760659ad8
名前 / ファイル ライセンス アクション
ME-PR-NAITO-H-12469.pdf ME-PR-NAITO-H-12469.pdf (2.3 MB)
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Item type 学術雑誌論文 / Journal Article(1)
公開日 2021-07-05
タイトル
タイトル Ligand-independent Tie2 dimers mediate kinase activity stimulated by high dose angiopoietin-1
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
ID登録
ID登録 10.24517/00062983
ID登録タイプ JaLC
著者 Yamakawa, Daishi

× Yamakawa, Daishi

WEKO 99325

Yamakawa, Daishi

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Kidoya, Hiroyasu

× Kidoya, Hiroyasu

WEKO 24114

Kidoya, Hiroyasu

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Sakimoto, Susumu

× Sakimoto, Susumu

WEKO 99287

Sakimoto, Susumu

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Jia, Weizhen

× Jia, Weizhen

WEKO 99331

Jia, Weizhen

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Naito, Hisamichi

× Naito, Hisamichi

WEKO 99339
e-Rad 30570676

Naito, Hisamichi

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Takakura, Nobuyuki

× Takakura, Nobuyuki

WEKO 15659
e-Rad 80291954
研究者番号 80291954

Takakura, Nobuyuki

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著者別表示 内藤, 尚道

× 内藤, 尚道

内藤, 尚道

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高倉, 伸幸

× 高倉, 伸幸

高倉, 伸幸

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提供者所属
内容記述タイプ Other
内容記述 金沢大学医薬保健研究域医学系
書誌情報 Journal of Biological Chemistry

巻 288, 号 18, p. 12469-12477, 発行日 2013-05-03
ISSN
収録物識別子タイプ ISSN
収録物識別子 0021-9258
ISSN
収録物識別子タイプ ISSN
収録物識別子 1083-351X
NCID
収録物識別子タイプ NCID
収録物識別子 AA00251083
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.1074/jbc.M112.433979
出版者
出版者 American Society for Biochemistry and Molecular Biology / Elsevier
抄録
内容記述タイプ Abstract
内容記述 Tie2 is a receptor tyrosine kinase expressed on vascular endothelial cells (ECs). It has dual roles in promoting angiogenesis and stabilizing blood vessels, and it has been suggested that Tie2 forms dimers and/or oligomers in the absence of angiopoietin-1 (Ang1); however, the mechanism of ligand-independent dimerization of Tie2 and its biological significance have not been clarified. Using a bimolecular fluorescence complementation assay and a kinase-inactive Tie2 mutant, we show here that ligand-independent Tie2 dimerization is induced without Tie2 phosphorylation. Moreover, based on the fact that Tie1 never forms heterodimers with Tie2 in the absence of Ang1 despite having high amino acid sequence homology with Tie2, we searched for ligand-independent dimerization domains of Tie2 by reference to the difference with Tie1. We found that the YIA sequence of the intracellular domain of Tie2 corresponding to the LAS sequence in Tie1 is essential for this dimerization. When the YIA sequence was replaced by LAS in Tie2 (Tie2YIA/LAS), ligand-independent dimer was not formed in the absence of Ang1. When activation of Tie2YIA/LAS was induced by a high dose of Ang1, phosphorylation of Tie2 was limited compared with wild-type Tie2, resulting in retardation of activation of Erk downstream of Tie2. Therefore, these data suggest that ligand-independent dimerization of Tie2 is essential for a strong response upon stimulation with high dose Ang1. © 2013 by The American Society for Biochemistry and Molecular Biology, Inc.
権利
権利情報 copyright © American Society for Biochemistry and Molecular Biology
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連URI
識別子タイプ URI
関連識別子 https://www.journals.elsevier.com/journal-of-biological-chemistry
関連名称 https://www.journals.elsevier.com/journal-of-biological-chemistry
関連URI
識別子タイプ URI
関連識別子 https://www.sciencedirect.com/science/article/pii/S0021925819333125?via%3Dihub
関連名称 https://www.sciencedirect.com/science/article/pii/S0021925819333125?via%3Dihub
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