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Hirata, Taku

Mayo Clinic

Mayo Clinic

Citations 13

Drosophila melanogaster as an Emerging Translational Model of Human Nephrolithiasis
Miller, Joe, Chi, Thomas , Kapahi, Pankaj , Kahn, Arnold, Hirata, Taku, Romero, Michael F. , Dow, Julian A. T. , Stoller, Marshall L. , Kim, Man Su , Dow, Julian A T , Romero, Michael F

Journal of Urology | March 8, 2013 | Volume: 190 | Issue: 5 | Pages: 1648-1656

10.1016/j.juro.2013.03.010 Get It

Identification and properties of a novel variant of NBC4 (Na+/HCO3− co-transporter 4) that is predominantly expressed in the choroid plexus
Fukuda, Hidekazu, Hirata, Taku, Nakamura, Nobuhiro , Kato, Akira , Kawahara, Katsumasa , Wakabayashi, Shigeo , Chang, Min‐Hwang , Romero, Michael F. , Hirose, Shigehisa , Romero, Michael F , Kato, Akira

Biochemical Journal | December 5, 2012 | Volume: 450 | Issue: 1 | Pages: 179-187

10.1042/bj20121515 Get It

Secretion of HCO3− at the apical side of the epithelial cells of the choroid plexus is an essential step in the formation of cerebrospinal fluid. Anion conductance with a high degree of HCO3− permeability has been observed and suggested to be the major pathway for HCO3− transport across the apical membrane. Recently, it was found that NBC (Na+/HCO3− co-transporter) 4, an electrogenic member of the NBC family, was expressed in the choroid plexus. We found that a novel variant of the NBC4 [NBC4g/Slc4a5 (solute carrier family 4, sodium bicarbonate co-transporter, member 5)] is almost exclusively expressed in the apical membrane of rat choroid plexus epithelium at exceptionally high levels. RNA interference-mediated knockdown allowed the functional demonstration that NBC4g is the major player in the HCO3− transport across the apical membrane of the choroid plexus epithelium. When combined with a recent observation that in choroid plexus epithelial cells electrogenic NBC operates with a stoichiometry of 3:1, the results of the present study suggest that NBC4g mediates the efflux of HCO3− and contributes to cerebrospinal fluid production.
In vivoDrosophiliagenetic model for calcium oxalate nephrolithiasis
Hirata, Taku, Cabrero, Pablo , Berkholz, Donald S., Bondeson, Daniel P. , Ritman, Erik L., Thompson, James R. , Dow, Julian A. T. , Romero, Michael F. , Dow, Julian A T , Romero, Michael F

American Journal of Physiology-Renal Physiology | September 20, 2012 | Volume: 303 | Issue: 11 | Pages: F1555-F1562

10.1152/ajprenal.00074.2012 Get It

Nephrolithiasis is a major public health problem with a complex and varied etiology. Most stones are composed of calcium oxalate (CaOx), with dietary excess a risk factor. Because of complexity of mammalian system, the details of stone formation remain to be understood. Here we have developed a nephrolithiasis model using the genetic model Drosophila melanogaster, which has a simple, transparent kidney tubule. Drosophilia reliably develops CaOx stones upon dietary oxalate supplementation, and the nucleation and growth of microliths can be viewed in real time. The Slc26 anion transporter dPrestin (Slc26a5/6) is strongly expressed in Drosophilia kidney, and biophysical analysis shows that it is a potent oxalate transporter. When dPrestin is knocked down by RNAi in fly kidney, formation of microliths is reduced, identifying dPrestin as a key player in oxalate excretion. CaOx stone formation is an ancient conserved process across >400 My of divergent evolution (fly and human), and from this study we can conclude that the fly is a good genetic model of nephrolithiasis.