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Characterization of urinary exosomal release of aquaporin-1 and -2 after renal ischemia-reperfusion in rats
http://hdl.handle.net/10458/0002000430
http://hdl.handle.net/10458/0002000430874848fa-1192-4b30-9ee1-023c77406017
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2024-01-09 | |||||
タイトル | ||||||
タイトル | Characterization of urinary exosomal release of aquaporin-1 and -2 after renal ischemia-reperfusion in rats | |||||
言語 | en | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
キーワード | ALG-2 interacting protein X | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
キーワード | aquaporin-1 | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
キーワード | aquaporin-2 | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
キーワード | exosomes | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
キーワード | extracellular vesicles | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
キーワード | renal fibrosis | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
キーワード | renal ischemia-reperfusion | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
キーワード | tumor susceptibility 101 protein | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
キーワード | urine | |||||
資源タイプ | ||||||
資源タイプ | journal article | |||||
アクセス権 | ||||||
著者 |
Siree, Asvapromtada
× Siree, Asvapromtada× 園田, 紘子× Kinouchi, Minami× Oshikawa, Sayaka× Takahashi, Saki× 星野, 雄也× ティタポーン, シンラパデレルドゥクル× Yokota-Ikeda, Naoko× Matsuzaki, Toshiyuki× 池田, 正浩 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Acute kidney injury (AKI) is an important risk factor for the development of chronic kidney disease (CKD), and an alteration in renal water handling has been observed during the transition of AKI to CKD. Urinary exosomal release of aquaporin-1 (AQP1) and AQP2, important proteins for renal water handling, has recently been reported to predict their levels of renal expression. Therefore, we examined the patterns of urinary exosomal release of AQP1 and AQP2, and the exosomal marker proteins tumor susceptibility 101 protein (TSG101) and ALG-2 interacting protein X (Alix), in the acute and chronic phases following induction of AKI by renal bilateral ischemia/reperfusion (I/R) in rats. Blood tests and histological examinations indicated that AKI occurred before at 7 days after renal I/R (day 7) and that renal fibrosis developed progressively thereafter. Immunoblotting demonstrated significant decreases in the urinary exosomal release of AQP1 and AQP2 during severe AKI. Urinary exosomal release of Alix and TSG101 was significantly increased on day 7. These data were also confirmed in rats with unilateral renal I/R causing more serious AKI. Urinary exosomal release of either the Ser-256- or Ser-269-phosphorylated form of AQP2, both of which are involved in apical trafficking of AQP2, was positively correlated with that of total AQP2. These results suggest that urinary exosomal release of AQP1 and AQP2 is reduced in I/R-induced AKI, whereas that of Alix and TSG101 is increased in the initial phase of renal fibrosis. Furthermore, apical trafficking of AQP2 appears to be related to urinary exosomal release of AQP2. | |||||
言語 | en | |||||
内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | Citation: Asvapromtada S, Sonoda H, Kinouchi M, Oshikawa S, Takahashi S, Hoshino Y, Sinlapadeelerdkul T, Yokota-Ikeda N, Matsuzaki T, Ikeda M. Characterization of urinary exosomal release of aquaporin-1 and -2 after renal ischemia-reperfusion in rats. Am J Physiol Renal Physiol. 2018 Apr 1;314(4):F584-F601. doi: 10.1152/ajprenal.00184.2017. Epub 2017 Dec 13. PMID: 29357442. |
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言語 | en | |||||
書誌情報 |
en : American Journal of Physiology-Renal Physiology 巻 314, 号 4, p. F584-F601, 発行日 2018-04-01 |
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出版者 | ||||||
出版者 | American Physical Society | |||||
言語 | en | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 1931-857X | |||||
DOI | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | DOI | |||||
関連識別子 | https://doi.org/10.1152/ajprenal.00184.2017 | |||||
著者版フラグ | ||||||
出版タイプ | NA |