c/ebpδ null mouse as a model for the double knock-out of slc5a8 and slc5a12 in kidney

Muthusamy Thangaraju, Sudha Ananth, Pamela M. Martin, Penny Roon, Sylvia B. Smith, Esta Sterneck, Puttur D. Prasad, Vadivel Ganapathy

Research output: Contribution to journalArticle

56 Scopus citations

Abstract

slc5a8 and slc5a12 represent the high affinity and low affinity Na +/lactate co-transporters, respectively, in the kidney. Here we show that these transporters are expressed in the apical membrane of the proximal tubular cells in mouse kidney, indicating that these transporters are likely to mediate the first step in the renal reabsorption of lactate. Interestingly, the renal expression of both transporters is almost completely ablated in mice homozygous for the deletion of the transcription factor c/ebpδ. This effect is tissue-specific since the expression of the transporters is not affected in non-renal tissues. The functional role of C/EBPδ in the expression of SLC5A8 and SLC5A12 is demonstrable in HEK293 cells in reporter assays using genespecific promoters. The ablation of the transporters in the kidney is accompanied by a marked increase in urinary excretion of lactate as well as a decrease in blood levels of lactate in c/ebpΔ-/- mice. These data provide evidence for an obligatory role for slc5a8 and slc5a12 in the renal absorption of lactate. In addition, we show that urinary excretion of urate is significantly elevated in c/ebpδ-/- mice even though the expression of URAT1, the transporter responsible for the apical membrane uptake of urate in renal proximal tubule, is not altered. These data provide in vivo evidence for the functional coupling between lactate reabsorption and urate reabsorption in the kidney. Thus, the fortuitous double knock-out of slc5a8 and slc5a12 in kidney in c/ebpδ-/- mice reveals the physiologic role of these transporters in the renal handling of lactate and urate.

Original languageEnglish (US)
Pages (from-to)26769-26773
Number of pages5
JournalJournal of Biological Chemistry
Volume281
Issue number37
DOIs
StatePublished - Sep 15 2006

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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