Activation of AQP2 water channels without vasopressin : therapeutic strategies for congenital nephrogenic diabetes insipidus

• 資料種別: 記事
• タイトル: Activation of AQP2 water channels without vasopressin : therapeutic strategies for congenital nephrogenic diabetes insipidus
• 著者・編者: Fumiaki Ando; Shinichi Uchida
• 出版事項: 日本 : Springer Nature
• 出版年月日等: 2018-02-24
• 出版年（W3CDTF）: 2018-02-24
• タイトル（掲載誌）: Clinical and experimental nephrology : official publication of the Japanese Society of Nephrology
• 巻号年月日等（掲載誌）: 22(3)
• 掲載巻: 22(3)
• ISSN（掲載誌）: 1437-7799
• ISSN-L（掲載誌）: 1437-7799
• 本文の言語コード: eng
• DOI: 10.1007/s10157-018-1544-8; https://doi.org/10.1007/s10157-018-1544-8
• 国立国会図書館永続的識別子: info:ndljp/pid/11636152; https://dl.ndl.go.jp/pid/11636152
• コレクション（共通）: 障害者向け資料
• コレクション（障害者向け資料：レベル1）: テキストデータ
• コレクション（個別）: 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他; https://dl.ndl.go.jp/collections/B00035
• 収集根拠: オンライン資料収集制度
• 受理日（W3CDTF）: 2021-02-10T20:40:42+09:00
• 保存日（W3CDTF）: 2021-01-27
• 記録形式（IMT）: application/pdf
• オンライン閲覧公開範囲: 国立国会図書館内限定公開
• デジタル化資料送信: 図書館・個人送信対象外
• 遠隔複写可否（NDL）: 可
• 掲載誌（URI）: https://link.springer.com/article/10.1007/s10157-018-1544-8
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/11636150; https://dl.ndl.go.jp/pid/11636150
• 連携機関・データベース: 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp

• 要約等: コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
• DOI: 10.1007/s10157-018-1544-8; https://doi.org/10.1007/s10157-018-1544-8
• 関連情報（URI）: http://id.ndl.go.jp/digimeta/11636152; https://dl.ndl.go.jp/pid/11636152; http://link.springer.com/article/10.1007/s10157-018-1544-8/fulltext.html; http://link.springer.com/content/pdf/10.1007/s10157-018-1544-8.pdf
• 参照: Tolvaptan activates the Nrf2/HO-1 antioxidant pathway through PERK phosphorylation; https://cir.nii.ac.jp/crid/1360568468327897472; Identification of protein kinase A signalling molecules in renal collecting ducts; https://cir.nii.ac.jp/crid/1360861705598388608; Activation of AQP2 water channels by protein kinase A : therapeutic strategies for congenital nephrogenic diabetes insipidus; https://cir.nii.ac.jp/crid/2051151842060103424
• 参照: Chapter 2 V2R Mutations and Nephrogenic Diabetes Insipidus; https://cir.nii.ac.jp/crid/1360011143689288192; Prostaglandin E2 synthesis and secretion: The role of PGE2 synthases; https://cir.nii.ac.jp/crid/1360011143963628800; Wnt5a induces renal AQP2 expression by activating calcineurin signalling pathway; https://cir.nii.ac.jp/crid/1360283691779394944; Reciprocal interaction with G-actin and tropomyosin is essential for aquaporin-2 trafficking; https://cir.nii.ac.jp/crid/1360283692363205888; Combination of secretin and fluvastatin ameliorates the polyuria associated with X-linked nephrogenic diabetes insipidus in mice; https://cir.nii.ac.jp/crid/1360292619163571712; Vasopressin-stimulated Increase in Phosphorylation at Ser269 Potentiates Plasma Membrane Retention of Aquaporin-2; https://cir.nii.ac.jp/crid/1360292620582051072; Long Term Regulation of Aquaporin-2 Expression in Vasopressin-responsive Renal Collecting Duct Principal Cells; https://cir.nii.ac.jp/crid/1360292621390247936; Corticosteroid-Dependent Sodium Transport in a Novel Immortalized Mouse Collecting Duct Principal Cell Line; https://cir.nii.ac.jp/crid/1360294647533190912; Regulation of Aquaporin-2 Trafficking by Vasopressin in the Renal Collecting Duct; https://cir.nii.ac.jp/crid/1360574094896367744; Wnt-5a/Ca²⁺-Induced NFAT Activity Is Counteracted by Wnt-5a/Yes-Cdc42-Casein Kinase 1α Signaling in Human Mammary Epithelial Cells; https://cir.nii.ac.jp/crid/1360574095445811712; Calcitonin Has a Vasopressin-like Effect on Aquaporin-2 Trafficking and Urinary Concentration; https://cir.nii.ac.jp/crid/1360574096348620672; Ser-261 phospho-regulation is involved in pS256 and pS269-mediated aquaporin-2 apical translocation; https://cir.nii.ac.jp/crid/1360848656932024960; Calmodulin: a prototypical calcium sensor; https://cir.nii.ac.jp/crid/1360855568741612672; Molecular mechanisms of angiotensin II stimulation on aquaporin-2 expression and trafficking; https://cir.nii.ac.jp/crid/1360855568924910464; Three Families with Autosomal Dominant Nephrogenic Diabetes Insipidus Caused by Aquaporin-2 Mutations in the C-Terminus; https://cir.nii.ac.jp/crid/1360855569300643840; Is There a Role for PGE2 in Urinary Concentration?; https://cir.nii.ac.jp/crid/1360855571209712384; Phosphorylation of Serine 256 Is Required for cAMP-dependent Regulatory Exocytosis of the Aquaporin-2 Water Channel; https://cir.nii.ac.jp/crid/1361137044022344192; Pathophysiology, diagnosis and management of nephrogenic diabetes insipidus; https://cir.nii.ac.jp/crid/1361137045137837056; AQP2 is a substrate for endogenous PP2B activity within an inner medullary AKAP-signaling complex; https://cir.nii.ac.jp/crid/1361137045669718912; The vasopressin type 2 receptor and prostaglandin receptors EP2 and EP4 can increase aquaporin-2 plasma membrane targeting through a cAMP-independent pathway; https://cir.nii.ac.jp/crid/1361418518573646464; Mechanisms of vasopressin-induced intracellular Ca²⁺oscillations in rat inner medullary collecting duct; https://cir.nii.ac.jp/crid/1361418520867632512; Regulation of aquaporin-2 trafficking and its binding protein complex; https://cir.nii.ac.jp/crid/1361699993533282176; cAMP regulates vasopressin-induced AQP2 expression via protein kinase A-independent pathway; https://cir.nii.ac.jp/crid/1361699993952412544; Epac-mediated Ca²⁺ mobilization and exocytosis in inner medullary collecting duct; https://cir.nii.ac.jp/crid/1361981468850422656; Nephrogenic Diabetes Insipidus: Essential Insights into the Molecular Background and Potential Therapies for Treatment; https://cir.nii.ac.jp/crid/1362262944255054848; Omega-6 Fatty Acids and Risk for Cardiovascular Disease; https://cir.nii.ac.jp/crid/1362262945134011520; Cellular Action of Vasopressin in Medullary Tubules of Mice with Hereditary Nephrogenic Diabetes Insipidus; https://cir.nii.ac.jp/crid/1362262945785233152; Renal expression of exchange protein directly activated by cAMP (Epac) 1 and 2; https://cir.nii.ac.jp/crid/1362262945832484864; Wnt-5a has tumor suppressor activity in thyroid carcinoma; https://cir.nii.ac.jp/crid/1362544418487798656; LIP5 Interacts with Aquaporin 2 and Facilitates Its Lysosomal Degradation; https://cir.nii.ac.jp/crid/1362544419824073344; Rolipram, a Phosphodiesterase Inhibitor, in the Treatment of Two Male Patients with Congenital Nephrogenic Diabetes insipidus; https://cir.nii.ac.jp/crid/1362544421270996608; Epac and PKA: a tale of two intracellular cAMP receptors; https://cir.nii.ac.jp/crid/1362825894844816768; In mpkCCD cells, long-term regulation of aquaporin-2 by vasopressin occurs independent of protein kinase A and CREB but may involve Epac; https://cir.nii.ac.jp/crid/1362825895133139840; Loss of calcineurin Aα results in altered trafficking of AQP2 and in nephrogenic diabetes insipidus; https://cir.nii.ac.jp/crid/1362825896034159616; Suppression of Cyclic GMP-dependent Protein Kinase Is Essential to the Wnt/cGMP/Ca2+ Pathway; https://cir.nii.ac.jp/crid/1363107369985139200; Dual Influence of Aldosterone on AQP2 Expression in Cultured Renal Collecting Duct Principal Cells; https://cir.nii.ac.jp/crid/1363107371204789504; Coupling of vasopressin‐induced intracellular Ca²⁺ mobilization and apical exocytosis in perfused rat kidney collecting duct; https://cir.nii.ac.jp/crid/1363388843390289920; Differential Expression of Calcineurin A Isoforms in the Diabetic Kidney; https://cir.nii.ac.jp/crid/1363388844059019008; Hypotonicity-induced Reduction of Aquaporin-2 Transcription in mpkCCD Cells Is Independent of the Tonicity Responsive Element, Vasopressin, and cAMP; https://cir.nii.ac.jp/crid/1363388844314510848; A selective EP4 PGE2 receptor agonist alleviates disease in a new mouse model of X-linked nephrogenic diabetes insipidus; https://cir.nii.ac.jp/crid/1363388844360765696; Nephrogenic Diabetes Insipidus; https://cir.nii.ac.jp/crid/1363388844563378304; Lithium reduces aquaporin-2 transcription independent of prostaglandins; https://cir.nii.ac.jp/crid/1363388845482320640; Calmodulin Is Required for Vasopressin-stimulated Increase in Cyclic AMP Production in Inner Medullary Collecting Duct; https://cir.nii.ac.jp/crid/1363388845611674112; Cell physiology of cAMP sensor Epac; https://cir.nii.ac.jp/crid/1363388846256461184; Downregulation of Renal Sodium Transporters and Tonicity-Responsive Enhancer Binding Protein by Long-Term Treatment with Cyclosporin A; https://cir.nii.ac.jp/crid/1363670318342157056; Dual Effects of Hypertonicity on Aquaporin-2 Expression in Cultured Renal Collecting Duct Principal Cells; https://cir.nii.ac.jp/crid/1363670318759875328; A Formylated Hexapeptide Ligand Mimics the Ability of Wnt-5a to Impair Migration of Human Breast Epithelial Cells; https://cir.nii.ac.jp/crid/1363670319407254912; Vasopressin-independent targeting of aquaporin-2 by selective E-prostanoid receptor agonists alleviates nephrogenic diabetes insipidus; https://cir.nii.ac.jp/crid/1363951793166990208; Phenotypes Developed in Secretin Receptor-Null Mice Indicated a Role for Secretin in Regulating Renal Water Reabsorption; https://cir.nii.ac.jp/crid/1363951794523754240; Calcineurin-NFATc signaling pathway regulates <i>AQP2</i> expression in response to calcium signals and osmotic stress; https://cir.nii.ac.jp/crid/1363951794899412864; Disruption of prostaglandin E2 receptor EP4 impairs urinary concentration via decreasing aquaporin 2 in renal collecting ducts; https://cir.nii.ac.jp/crid/1363951795087355008; Counteracting vasopressin-mediated water reabsorption by ATP, dopamine, and phorbol esters: mechanisms of action; https://cir.nii.ac.jp/crid/1363951795263828736; Insulin potentiates AVP-induced AQP2 expression in cultured renal collecting duct principal cells; https://cir.nii.ac.jp/crid/1364233268664823168; Phosphorylation events and the modulation of aquaporin 2 cell surface expression; https://cir.nii.ac.jp/crid/1364233269272870272; Pathogenesis and treatment of autosomal-dominant nephrogenic diabetes insipidus caused by an aquaporin 2 mutation; https://cir.nii.ac.jp/crid/1364233271121642752; Faculty Opinions recommendation of The vasopressin type 2 receptor and prostaglandin receptors EP2 and EP4 can increase aquaporin-2 plasma membrane targeting through a cAMP-independent pathway.; https://cir.nii.ac.jp/crid/1881146593280015616; Faculty Opinions recommendation of Hypotonicity-induced reduction of aquaporin-2 transcription in mpkCCD cells is independent of the tonicity responsive element, vasopressin, and cAMP.; https://cir.nii.ac.jp/crid/1883961342349140608
• 連携機関・データベース: 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• 提供元機関・データベース: 雑誌記事索引データベース; https://ndlsearch.ndl.go.jp; Crossref; https://www.crossref.org; 科学研究費助成事業データベース; https://kaken.nii.ac.jp/ja
• 書誌ID（NDLBibID）: 11636152; http://id.ndl.go.jp/bib/11636152