4.6 Article

Acidosis and alkali therapy in patients with kidney transplant is associated with transcriptional changes and altered abundance of genes involved in cell metabolism and acid-base balance

Journal

NEPHROLOGY DIALYSIS TRANSPLANTATION
Volume 36, Issue 10, Pages 1806-1820

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ndt/gfab210

Keywords

alkali therapy; bicarbonate; cell metabolism; kidney biopsy; metabolic acidosis; renal transplant; transcriptome

Funding

  1. Swiss National Science Foundation (SNSF)
  2. SNSF-funded National Centre of Competence in Research NCCR Kidney.CH
  3. Hartmann Mu ller Foundation

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Metabolic acidosis in kidney transplant recipients is associated with changes in the renal transcriptome, with 40 transcripts significantly altered between non-acidotic and acidotic patients, primarily affecting genes involved in proximal tubule amino acid and lipid metabolism as well as energy homeostasis. Alkali therapy partially restores the expression of certain genes related to PT HCO3- metabolism and transport.
Background. Metabolic acidosis occurs frequently in patients with kidney transplant and is associated with a higher risk for and accelerated loss of graft function. To date, it is not known whether alkali therapy in these patients improves kidney function and whether acidosis and its therapy are associated with altered expression of proteins involved in renal acid-base metabolism. Methods. We retrospectively collected kidney biopsies from 22 patients. Of these patients, nine had no acidosis, nine had metabolic acidosis [plasma bicarbonate (HCO3-<22mmol/L) and four had acidosis and received alkali therapy. We performed transcriptome analysis and immunohistochemistry for proteins involved in renal acid-base handling. Results. We found that the expression of 40 transcripts significantly changed between kidneys from non-acidotic and acidotic patients. These genes are mostly involved in proximal tubule (PT) amino acid and lipid metabolism and energy homoeostasis. Three transcripts were fully recovered by alkali therapy: the Kir4.2 potassium channel, an important regulator of PT HCO3- metabolism and transport, acyl-CoA dehydrogenase short/branched chain and serine hydroxymethyltransferase 1, genes involved in beta oxidation and methionine metabolism. Immunohistochemistry showed reduced staining for the PT NBCe1 HCO3- transporter in kidneys from acidotic patients who recovered with alkali therapy. In addition, the HCO3- exchanger pendrin was affected by acidosis and alkali therapy. Conclusions. Metabolic acidosis in kidney transplant recipients is associated with alterations in the renal transcriptome that are partly restored by alkali therapy. Acid-base transport proteins mostly from PT were also affected by acidosis and alkali therapy, suggesting that the downregulation of critical players contributes to metabolic acidosis in these patients.

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