Evidence map›Paper›PMID 25281699›Full record

ReviewNephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association2015

The multiple roles of pendrin in the kidney.

Manoocher Soleimani

Open access · bronzeAbstract readReview
In one paragraph

Review in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 60 citations in OpenAlex.

  1. Low Dietary Iodine Intake and Sex-Specific Mortality in Kidney Transplant Recipients.Clinical journal of the American Society of Nephrology : CJASN · 2026
    Observational
  2. Article
  3. Review
  4. Article
  5. A 23-year-old woman with metabolic alkalosis and hypokalemia.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Metabolic Alkalosis Pathogenesis, Diagnosis, and Treatment: Core Curriculum 2022.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2022
    Review
  11. Molecular Features of SLC26A4 Common Variant p.L117F.Journal of clinical medicine · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Dysnatremia in Gastrointestinal Disorders.Frontiers in medicine · 2022
    Review
  17. Review
  18. Review
  19. Article
  20. "I don't get no respect": the role of chloride in acute kidney injury.American journal of physiology. Renal physiology · 2019
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Manoocher SoleimaniCenter on Genetics of Transport and Epithelial Biology, University of Cincinnati, Cincinnati, OH, USA Research Services, Veterans Affairs Medical Center, Cincinnati, OH, USA Department of Medicine, University of Cincinnati, Cincinnati, OH, USA.
University of Cincinnati · US

Funding

Apical CI/OH-/HCO3-exchanger in kidney and GI tractR01DK062809 · NIDDK · UNIVERSITY OF CINCINNATI · PI SOLEIMANI, MANOOCHER · 2004 to 2007
$1.5M
Apical Chloride/Bicarbonate Exchangers in Small Intestine and KidneyR56DK062809 · NIDDK · UNIVERSITY OF CINCINNATI · PI SOLEIMANI, MANOOCHER · 2009 to 2009
$461k
NIDDK NIH HHS R01 DK62809NIDDK NIH HHS R56DK62809
6 · The paper itself

Abstract

The [Formula: see text] exchanger pendrin (SLC26A4, PDS) is located on the apical membrane of B-intercalated cells in the kidney cortical collecting duct and the connecting tubules and mediates the secretion of bicarbonate and the reabsorption of chloride. Given its dual function of bicarbonate secretion and chloride reabsorption in the distal tubules, it was thought that pendrin plays important roles in systemic acid-base balance and electrolyte and vascular volume homeostasis under basal conditions. Mice with the genetic deletion of pendrin or humans with inactivating mutations in PDS gene, however, do not display excessive salt and fluid wasting or altered blood pressure under baseline conditions. Very recent reports have unmasked the basis of incongruity between the mild phenotype in mutant mice and the role of pendrin as an important player in salt reabsorption in the distal tubule. These studies demonstrate that pendrin and the Na-Cl cotransporter (NCC; SLC12A3) cross compensate for the loss of each other, therefore masking the role that each transporter plays in salt reabsorption under baseline conditions. In addition, pendrin regulates calcium reabsorption in the distal tubules. Furthermore, combined deletion of pendrin and NCC not only causes severe volume depletion but also results in profound calcium wasting and luminal calcification in medullary collecting ducts. Based on studies in pathophysiological states and the examination of genetically engineered mouse models, the evolving picture points to important roles for pendrin (SLC26A4) in kidney physiology and in disease states. This review summarizes recent advances in the characterization of pendrin and the multiple roles it plays in the kidney, with emphasis on its essential roles in several diverse physiological processes, including chloride homeostasis, vascular volume and blood pressure regulation, calcium excretion and kidney stone formation.

Indexed as

Acid-Base EquilibriumAnimalsAnion Transport ProteinsHumansKidney DiseasesMembrane Transport ProteinsMiceSolute Carrier Family 12, Member 3Sulfate TransportersWater-Electrolyte BalanceAnion Transport ProteinsMembrane Transport ProteinsSLC12A3 protein, humanSlc12a3 protein, mouseSLC26A4 protein, humanSlc26a4 protein, mouseSolute Carrier Family 12, Member 3Sulfate Transportershypertensionoxalate stonerenal tubular acidosissalt excretionvolume depletion

Identifiers

PMID25281699
PMCPMC4513892
OpenAlexW2064143634

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.