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

• Published in: Nephrology, dialysis, transplantation Vol. 36; no. 10; pp. 1806 - 1820
• Main Authors: Imenez Silva, Pedro H, Wiegand, Anna, Daryadel, Arezoo, Russo, Giancarlo, Ritter, Alexander, Gaspert, Ariana, Wüthrich, Rudolf P, Wagner, Carsten A, Mohebbi, Nilufar
• Format: Journal Article
• Language: English
• Published: Oxford University Press 01.10.2021
• Subjects: metabolic acidosis; kidney biopsy; transcriptome; renal transplant; cell metabolism; bicarbonate; alkali therapy
• ISSN: 0931-0509; 1460-2385
• DOI: 10.1093/ndt/gfab210

Abstract 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− <22 mmol/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. Graphical Abstract