Literature DB >> 30671592

Regulation of α-Klotho Expression by Dietary Phosphate During Growth Periods.

Shiori Fukuda-Tatano1,2, Hironori Yamamoto1,3,4, Otoki Nakahashi1,5, Ryouhei Yoshikawa1, Mayu Hayashi1, Maki Kishimoto1, Yukiko Imi6, Hisami Yamanaka-Okumura1, Kohta Ohnishi1, Masashi Masuda1, Yutaka Taketani7.   

Abstract

Inorganic phosphate (Pi) is an essential nutrient for maintaining various biological functions, particularly during growth periods. Excess intake of dietary Pi increases the secretion of fibroblast growth factor 23 (FGF23) and parathyroid hormone to maintain plasma Pi levels. FGF23 is a potent phosphaturic factor that binds to the α-klotho/FGFR complex in the kidney to promote excretion of Pi into the urine. In addition, excess intake of dietary Pi decreases renal α-klotho expression. Down-regulation or lack of α-klotho induces a premature aging-like phenotype, resulting from hyperphosphatemia, and leading to conditions such as ectopic calcification and osteoporosis. However, it remains unclear what effects dietary Pi has on α-klotho expression at different life stages, especially during growth periods. To investigate this, we used C57BL/6J mice in two life stages during growing period. Weaned (3 weeks old) and periadolescent (7 weeks old) were randomly divided into seven experimental groups and fed with 0.02, 0.3, 0.6, 0.9, 1.2, 1.5, or 1.8% Pi diets for 7 days. As a result, elevated plasma Pi and FGF23 levels and decreased renal α-klotho expression were observed in weaned mice fed with a high Pi diet. In addition, a high Pi diet clearly induced renal calcification in the weaned mice. However, in the periadolescent group, renal calcification was not observed, even in the 1.8% Pi diet group. The present study indicates that a high Pi diet in weaned mice has much greater adverse effects on renal α-klotho expression and pathogenesis of renal calcification compared with periadolescent mice.

Entities:  

Keywords:  Dietary phosphate; FGF23; Growth periods; Kidney; Vitamin D metabolism; α-Klotho

Year:  2019        PMID: 30671592     DOI: 10.1007/s00223-019-00525-0

Source DB:  PubMed          Journal:  Calcif Tissue Int        ISSN: 0171-967X            Impact factor:   4.333


  6 in total

1.  Phosphate and Cellular Senescence.

Authors:  Ming Chang Hu; Orson W Moe
Journal:  Adv Exp Med Biol       Date:  2022       Impact factor: 3.650

2.  The Clinical Value of Klotho and FGF23 in Cardiac Valve Calcification Among Patients with Chronic Kidney Disease.

Authors:  Yan Chen; Yan-Xia Chen; Chong Huang; Zhi-Bing Duan; Cheng-Yun Xu
Journal:  Int J Gen Med       Date:  2021-03-15

3.  Sugar sweetened beverage consumption is positively associated with Klotho levels at two years of age in LatinX youth.

Authors:  Sofia Villagomez; Dena B Dubal; Jessica Hawkins; Dan Wang; Janet M Wojcicki
Journal:  BMC Nutr       Date:  2021-04-23

Review 4.  Understanding the Stony Bridge between Osteoporosis and Vascular Calcification: Impact of the FGF23/Klotho axis.

Authors:  Xu Wei; Xinyi Huang; Ning Liu; Baoyu Qi; Shengjie Fang; Yili Zhang
Journal:  Oxid Med Cell Longev       Date:  2021-08-30       Impact factor: 6.543

5.  25-hydroxyvitamin D-1α-hydroxylase (CYP27B1) induces ectopic calcification.

Authors:  Yilimulati Yimamu; Ayako Ohtani; Yuichiro Takei; Airi Furuichi; Yuki Kamei; Hisami Yamanaka-Okumura; Hirokazu Ohminami; Masashi Masuda; Makoto Miyazaki; Hironori Yamamoto; Yutaka Taketani
Journal:  J Clin Biochem Nutr       Date:  2022-06-04       Impact factor: 3.179

6.  High Phosphate Induces and Klotho Attenuates Kidney Epithelial Senescence and Fibrosis.

Authors:  Jenny Maique; Brianna Flores; Mingjun Shi; Sierra Shepard; Zhiyong Zhou; Shirely Yan; Orson W Moe; Ming Chang Hu
Journal:  Front Pharmacol       Date:  2020-08-20       Impact factor: 5.810

  6 in total

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