Evidence map›Paper›PMID 19073637›Full record

ArticleAmerican journal of physiology. Renal physiology2009

The Na+-Pi cotransporter PiT-2 (SLC20A2) is expressed in the apical membrane of rat renal proximal tubules and regulated by dietary Pi.

Ricardo Villa-Bellosta, Silvia Ravera, Victor Sorribas, Gerti Stange, Moshe Levi, Heini Murer, Jürg Biber, Ian C Forster

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

70 citing papers in PubMed, 169 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Updates on renal phosphate transport.Current opinion in nephrology and hypertension · 2025
    Review
  6. Article
  7. Article
  8. The Intricacies of Renal Phosphate Reabsorption-An Overview.International journal of molecular sciences · 2024
    Review
  9. Current perspective on circadian function of the kidney.American journal of physiology. Renal physiology · 2024
    Review
  10. Pharmacology of Mammalian NaHandbook of experimental pharmacology · 2024
    Article
  11. Article
  12. Review
  13. Article
  14. Phosphate intake, hyperphosphatemia, and kidney function.Pflugers Archiv : European journal of physiology · 2022
    Review
  15. Vitamin D and Phosphate Interactions in Health and Disease.Advances in experimental medicine and biology · 2022
    Article
  16. Article
  17. Hormonal regulation of biomineralization.Nature reviews. Endocrinology · 2021
    Review
  18. Phosphate as a Signaling Molecule.Calcified tissue international · 2021
    Review
  19. Developmental Changes in Phosphate Homeostasis.Reviews of physiology, biochemistry and pharmacology · 2021
    Review
  20. Article

10 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Ricardo Villa-BellostaInstitute of Physiology, Univ. of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
Silvia Ravera
Victor Sorribas
Gerti Stange
Moshe Levi
Heini Murer
Jürg Biber
Ian C Forster
ZHAW Zurich University of Applied Sciences · CH

Funding

Regulation of Renal Phosphate Transport by LipidsR01DK066029 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LEVI, MOSHE · 2005 to 2013
$3.2M
NIDDK NIH HHS R01 DK-066029
6 · The paper itself

Abstract

The principal mediators of renal phosphate (P(i)) reabsorption are the SLC34 family proteins NaPi-IIa and NaPi-IIc, localized to the proximal tubule (PT) apical membrane. Their abundance is regulated by circulatory factors and dietary P(i). Although their physiological importance has been confirmed in knockout animal studies, significant P(i) reabsorptive capacity remains, which suggests the involvement of other secondary-active P(i) transporters along the nephron. Here we show that a member of the SLC20 gene family (PiT-2) is localized to the brush-border membrane (BBM) of the PT epithelia and that its abundance, confirmed by Western blot and immunohistochemistry of rat kidney slices, is regulated by dietary P(i). In rats treated chronically on a high-P(i) (1.2%) diet, there was a marked decrease in the apparent abundance of PiT-2 protein in kidney slices compared with those from rats kept on a chronic low-P(i) (0.1%) diet. In Western blots of BBM from rats that were switched from a chronic low- to high-P(i) diet, NaPi-IIa showed rapid downregulation after 2 h; PiT-2 was also significantly downregulated at 24 h and NaPi-IIc after 48 h. For the converse dietary regime, NaPi-IIa showed adaptation within 8 h, whereas PiT-2 and NaPi-IIc showed a slower adaptive trend. Our findings suggest that PiT-2, until now considered as a ubiquitously expressed P(i) housekeeping transporter, is a novel mediator of P(i) reabsorption in the PT under conditions of acute P(i) deprivation, but with a different adaptive time course from NaPi-IIa and NaPi-IIc.

Indexed as

DietAdaptation, PhysiologicalAnimalsBiological TransportBlotting, WesternCell MembraneCell PolarityImmunohistochemistryKidney Tubules, ProximalMaleMicrovilliPhosphatesRatsRats, WistarSodium-Phosphate Cotransporter Proteins, Type IISodium-Phosphate Cotransporter Proteins, Type IIIPhosphatesSlc20a2 protein, ratSodium-Phosphate Cotransporter Proteins, Type IISodium-Phosphate Cotransporter Proteins, Type III

Identifiers

PMID19073637
PMCPMC2670642
OpenAlexW2155096876

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.