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ID 113363
Title Alternative
ヒト腎臓におけるリン代謝機構を理解するためのオポッサム腎NaPi-IIc (Na+依存性Piトランスポーター)の解析
Author
Fujii, Toru University of Tokushima
Nishiguchi, Shiori University of Tokushima
Hanazaki, Ai University of Tokushima
Noguchi, Miwa University of Tokushima
Kirino, Ruri University of Tokushima
Sasaki, Sumire University of Tokushima
Tanifuji, Kazuya University of Tokushima
Koike, Megumi University of Tokushima
Yokoyama, Mizuki University of Tokushima
Arima, Yuki University of Tokushima
Kaneko, Ichiro University of Tokushima KAKEN Search Researchers
Ito, Mikiko University of Hyogo
Keywords
Phosphate
Transporter
Proximal tubule
Hereditary hypophosphatemic rickets with hypercalciuria
Content Type
Thesis or Dissertation
Description
Background The role of Na+- dependent inorganic phosphate (Pi) transporters in the human kidney is not fully clarified. Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is caused by loss-of-function mutations in the IIc Na+- dependent Pi transporter (NPT2c/Npt2c/NaPi-IIc) gene. Another Na+- dependent type II transporter, (NPT2A/Npt2a/NaPi-IIa), is also important for renal Pi reabsorption in humans. In mice, Npt2c deletion does not lead to hypophosphatemia and rickets because Npt2a compensates for the impaired Pi reabsorption. To clarify the differences between mouse and human, we investigated the relation between NaPi-IIa and NaPi-IIc functions in opossum kidney (OK) cells.
Methods We cloned NaPi-IIc from OK cells and created opossum NaPi-IIc (oNaPi-IIc) antibodies. We used oNaPi-IIc small interference (si)RNA and investigated the role of NaPi-IIc in Pi transport in OK cells.
Results We cloned opossum kidney NaPi-IIc cDNAs encoding 622 amino acid proteins (variant1) and examined their pH- and sodium-dependency. The antibodies reacted specifically with 75-kDa and 150-kDa protein bands, and the siRNA of NaPi-IIc markedly suppressed endogenous oNaPi-IIc in OK cells. Treatment with siRNA significantly suppressed the expression of NaPi-4 (NaPi-IIa) protein and mRNA. oNaPi-IIc siRNA also suppressed Na+/H+ exchanger regulatory factor 1 expression in OK cells.
Conclusion These findings suggest that NaPi-IIc is important for the expression of NaPi-IIa (NaPi-4) protein in OK cells. Suppression of Npt2c may downregulate Npt2a function in HHRH patients.
Journal Title
Clinical and Experimental Nephrology
ISSN
13421751
14377799
NCID
AA11126935
Publisher
Japanese Society of Nephrology|Springer
Volume
23
Issue
3
Start Page
313
End Page
324
Published Date
2018-10-13
Remark
内容要旨・審査要旨・論文本文の公開
本論文は,著者Toru Fujiiの学位論文として提出され,学位審査・授与の対象となっている。
The final publication is available at Springer via https://doi.org/10.1007/s10157-018-1653-4
Rights
© Japanese Society of Nephrology 2018
EDB ID
DOI (Published Version)
URL ( Publisher's Version )
FullText File
language
eng
TextVersion
ETD
MEXT report number
甲第3273号
Diploma Number
甲栄第262号
Granted Date
2019-03-22
Degree Name
Doctor of Nutritional Science
Grantor
Tokushima University
departments
Medical Sciences