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Tmem174, a regulator of phosphate transporter prevents hyperphosphatemia

https://tokushima-u.repo.nii.ac.jp/records/2012850
https://tokushima-u.repo.nii.ac.jp/records/2012850
55955aaa-c1fc-411d-8a24-ee96dc31ccf6
名前 / ファイル ライセンス アクション
srep_12_6353.pdf srep_12_6353.pdf (2.7 MB)
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Item type 文献 / Documents(1)
公開日 2025-05-19
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
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
出版社版DOI
関連識別子 https://doi.org/10.1038/s41598-022-10409-3
関連名称 10.1038/s41598-022-10409-3
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
タイトル
タイトル Tmem174, a regulator of phosphate transporter prevents hyperphosphatemia
著者 Sasaki, Sumire

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en Sasaki, Sumire

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塩﨑, 雄治

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徳島大学 教育研究者総覧 375089/profile-ja.html

ja 塩﨑, 雄治

ja-Kana シオザキ, ユウヂ

en Shiozaki, Yuji

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Hanazaki, Ai

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小池, 萌

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徳島大学 教育研究者総覧 405934/profile-ja.html
e-Rad_Researcher 71000064

ja 小池, 萌

ja-Kana コイケ, メグミ

en Koike, Megumi

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Tanifuji, Kazuya

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Uga, Minori

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Kawahara, Kota

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金子, 一郎

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徳島大学 教育研究者総覧 277610/profile-ja.html
e-Rad_Researcher 40389515

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ja-Kana カネコ, イチロウ

en Kaneko, Ichiro

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Kawamoto, Yasuharu

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Wiriyasermkul, Pattama

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Hasegawa, Tomoka

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Amizuka, Norio

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宮本, 賢一

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ja-Kana ミヤモト, ケンイチ

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Nagamori, Shushi

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Kanai, Yoshikatsu

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瀬川, 博子

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抄録
内容記述 Renal type II sodium-dependent inorganic phosphate (Pi) transporters NaPi2a and NaPi2c cooperate with other organs to strictly regulate the plasma Pi concentration. A high Pi load induces expression and secretion of the phosphaturic hormones parathyroid hormone (PTH) and fibroblast growth factor 23 (FGF23) that enhance urinary Pi excretion and prevent the onset of hyperphosphatemia. How FGF23 secretion from bone is increased by a high Pi load and the setpoint of the plasma Pi concentration, however, are unclear. Here, we investigated the role of Transmembrane protein 174 (Tmem174) and observed evidence for gene co-expression networks in NaPi2a and NaPi2c function. Tmem174 is localized in the renal proximal tubules and interacts with NaPi2a, but not NaPi2c. In Tmem174-knockout (KO) mice, the serum FGF23 concentration was markedly increased but increased Pi excretion and hypophosphatemia were not observed. In addition, Tmem174-KO mice exhibit reduced NaPi2a responsiveness to FGF23 and PTH administration. Furthermore, a dietary Pi load causes marked hyperphosphatemia and abnormal NaPi2a regulation in Tmem174-KO mice. Thus, Tmem174 is thought to be associated with FGF23 induction in bones and the regulation of NaPi2a to prevent an increase in the plasma Pi concentration due to a high Pi load and kidney injury.
書誌情報 en : Scientific Reports

巻 12, p. 6353, 発行日 2022-04-15
収録物ID
収録物識別子タイプ EISSN
収録物識別子 20452322
出版者
出版者 Springer Nature
権利情報
権利情報 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
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識別子 387857
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言語 eng
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