Functional regulation of von Willebrand factor ameliorates acute ischemia-reperfusion kidney injury in mice.

• Material Type: 博士論文
• Title: Functional regulation of von Willebrand factor ameliorates acute ischemia-reperfusion kidney injury in mice.
• Author/Editor: Ono, Shiro; Matsui, Hideto; Noda, Masashi; Kasuda, Shogo; Yada, Noritaka; Yoshimoto, Kiyomi; Akiyama, Masashi; Miyata, Toshiyuki; Sugimoto, Mitsuhiko; Nishio, Kenji
• Author Heading: Ono, Shiro; Matsui, Hideto; Noda, Masashi; Kasuda, Shogo; Yada, Noritaka; Yoshimoto, Kiyomi; Akiyama, Masashi; Miyata, Toshiyuki; Sugimoto, Mitsuhiko; Nishio, Kenji
• Publication, Distribution, etc.: Springer Nature
• Publication Date: 2019-10
• Publication Date (W3CDTF): 2019-10
• Alternative Title: フォン・ヴィレブランド因子の機能を調節することで、マウスの急性腎虚血再灌流障害を緩和できる
• Periodical title: Scientific reports
• No. or year of volume/issue: 9 1
• Volume: 9
• Issue: 1
• Pages: Article No.14453-
• ISSN (Periodical Title): ISSN : 2045-2322
• Degree grantor/type: 奈良県立医科大学
• Date Granted: 2020-03-16
• Dissertation Number: 甲第744号
• Degree Type: 博士（医学）
• Text Language Code: eng
• Subject Heading: Biochemistry; Physiology
• Target Audience: 一般
• Note (General): type:Thesis; Acute kidney injury (AKI), an abrupt loss of renal function, is often seen in clinical settings and may become fatal. In addition to its hemostatic functions, von Willebrand factor (VWF) is known to play a role in cross-talk between inflammation and thrombosis. We hypothesized that VWF may be involved in the pathophysiology of AKI, major causes of which include insufficient renal circulation or inflammatory cell infiltration in the kidney. To test this hypothesis, we studied the role of VWF in AKI using a mouse model of acute ischemia-reperfusion (I/R) kidney injury. We analyzed renal function and blood flow in VWF-gene deleted (knock-out; KO) mice. The functional regulation of VWF by ADAMTS13 or a function-blocking anti-VWF antibody was also evaluated in this pathological condition. Greater renal blood flow and lower serum creatinine were observed after reperfusion in VWF-KO mice compared with wild-type (WT) mice. Histological analysis also revealed a significantly lower degree of tubular damage and neutrophil infiltration in kidney tissues of VWF-KO mice. Both human recombinant ADAMTS13 and a function-blocking anti-VWF antibody significantly improved renal blood flow, renal function and histological findings in WT mice. Our results indicate that VWF plays a role in the pathogenesis of AKI. Proper functional regulation of VWF may improve the microcirculation and vessel function in the kidney, suggesting a novel therapeutic option against AKI.; 博士（医学）・甲第744号・令和2年3月16日; © The Author(s) 2019. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.; identifier:Scientific reports Vol.9 No.1 Article No.14453 (2019 Oct); identifier:20452322; identifier:http://ginmu.naramed-u.ac.jp/dspace/handle/10564/3738; identifier:Scientific reports, 9(1): Article No.14453
• Source: fulltext; http://ginmu.naramed-u.ac.jp/dspace/bitstream/10564/3738/1/01%e7%94%b2744%e6%9c%ac%e6%96%87%e3%81%ae%e8%a6%81%e6%97%a8.pdf; http://ginmu.naramed-u.ac.jp/dspace/bitstream/10564/3738/2/02%e7%94%b2744%e5%af%a9%e6%9f%bb%e8%a6%81%e6%97%a8.pdf; http://ginmu.naramed-u.ac.jp/dspace/bitstream/10564/3738/3/03%e7%94%b2744%e6%9c%ac%e6%96%87.pdf
• Access Restrictions: インターネット公開
• Related Material (DOI): 10.1038/s41598-019-51013-2
• Data Provider (Database): 国立情報学研究所 : 学術機関リポジトリデータベース（IRDB）（機関リポジトリ）; https://irdb.nii.ac.jp
• Original Data Provider (Database): 奈良県立医科大学 : 奈良県立医科大学機関リポジトリ GINMU