Sulfate and thiosulfate inhibit oxalate transport via a dPrestin (Slc26a6)-dependent mechanism in an insect model of calcium oxalate nephrolithiasis

Greg M. Landry, Taku Hirata, Jacob B. Anderson, Pablo Cabrero, Christopher J R Gallo, Julian A T Dow, Michael F Romero

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Nephrolithiasis is one of the most common urinary tract disorders, with the majority of kidney stones composed of calcium oxalate (CaOx). Given its prevalence (US occurrence 10%), it is still poorly understood, lacking progress in identifying new therapies because of its complex etiology. Drosophila melanogaster (fruitfly) is a recently developed model of CaOx nephrolithiasis. Effects of sulfate and thiosulfate on crystal formation were investigated using the Drosophila model, as well as electrophysiological effects on both Drosophila (Slc26a5/6; dPrestin) and mouse (mSlc26a6) oxalate transporters utilizing the Xenopus laevis oocyte heterologous expression system. Results indicate that both transport thiosulfate with a much higher affinity than sulfate Additionally, both compounds were effective at decreasing CaOx crystallization when added to the diet. However, these results were not observed when compounds were applied to Malpighian tubules ex vivo. Neither compound affected CaOx crystallization in dPrestin knockdown animals, indicating a role for principal cell-specific dPrestin in luminal oxalate transport. Furthermore, thiosulfate has a higher affinity for dPrestin and mSlc26a6 compared with oxalate These data indicate that thiosulfate's ability to act as a competitive inhibitor of oxalate via dPrestin, can explain the decrease in CaOx crystallization seen in the presence of thiosulfate, but not sulfate. Overall, our findings predict that thiosulfate or oxalate-mimics may be effective as therapeutic competitive inhibitors of CaOx crystallization.

Original languageEnglish (US)
Pages (from-to)F152-F159
JournalAmerican Journal of Physiology - Renal Physiology
Volume310
Issue number2
DOIs
StatePublished - Nov 4 2015

Fingerprint

Thiosulfates
Oxalates
Calcium Oxalate
Sulfates
Insects
Crystallization
Drosophila
Malpighian Tubules
Nephrolithiasis
Kidney Calculi
Xenopus laevis
Drosophila melanogaster
Urinary Tract
Oocytes
Calcium Oxalate Nephrolithiasis
Diet
Therapeutics

Keywords

  • Electrophysiology
  • Inhibition
  • Kinetics
  • Oxalate
  • Slc26a6
  • Sulfate
  • Thiosulfate
  • Transport

ASJC Scopus subject areas

  • Physiology
  • Urology

Cite this

Sulfate and thiosulfate inhibit oxalate transport via a dPrestin (Slc26a6)-dependent mechanism in an insect model of calcium oxalate nephrolithiasis. / Landry, Greg M.; Hirata, Taku; Anderson, Jacob B.; Cabrero, Pablo; Gallo, Christopher J R; Dow, Julian A T; Romero, Michael F.

In: American Journal of Physiology - Renal Physiology, Vol. 310, No. 2, 04.11.2015, p. F152-F159.

Research output: Contribution to journalArticle

Landry, Greg M. ; Hirata, Taku ; Anderson, Jacob B. ; Cabrero, Pablo ; Gallo, Christopher J R ; Dow, Julian A T ; Romero, Michael F. / Sulfate and thiosulfate inhibit oxalate transport via a dPrestin (Slc26a6)-dependent mechanism in an insect model of calcium oxalate nephrolithiasis. In: American Journal of Physiology - Renal Physiology. 2015 ; Vol. 310, No. 2. pp. F152-F159.
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abstract = "Nephrolithiasis is one of the most common urinary tract disorders, with the majority of kidney stones composed of calcium oxalate (CaOx). Given its prevalence (US occurrence 10{\%}), it is still poorly understood, lacking progress in identifying new therapies because of its complex etiology. Drosophila melanogaster (fruitfly) is a recently developed model of CaOx nephrolithiasis. Effects of sulfate and thiosulfate on crystal formation were investigated using the Drosophila model, as well as electrophysiological effects on both Drosophila (Slc26a5/6; dPrestin) and mouse (mSlc26a6) oxalate transporters utilizing the Xenopus laevis oocyte heterologous expression system. Results indicate that both transport thiosulfate with a much higher affinity than sulfate Additionally, both compounds were effective at decreasing CaOx crystallization when added to the diet. However, these results were not observed when compounds were applied to Malpighian tubules ex vivo. Neither compound affected CaOx crystallization in dPrestin knockdown animals, indicating a role for principal cell-specific dPrestin in luminal oxalate transport. Furthermore, thiosulfate has a higher affinity for dPrestin and mSlc26a6 compared with oxalate These data indicate that thiosulfate's ability to act as a competitive inhibitor of oxalate via dPrestin, can explain the decrease in CaOx crystallization seen in the presence of thiosulfate, but not sulfate. Overall, our findings predict that thiosulfate or oxalate-mimics may be effective as therapeutic competitive inhibitors of CaOx crystallization.",
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AU - Hirata, Taku

AU - Anderson, Jacob B.

AU - Cabrero, Pablo

AU - Gallo, Christopher J R

AU - Dow, Julian A T

AU - Romero, Michael F

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