Evidence map›Paper›PMID 8643577›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1996

Expression of a renal type I sodium/phosphate transporter (NaPi-1) induces a conductance in Xenopus oocytes permeable for organic and inorganic anions.

A E Busch, A Schuster, S Waldegger, C A Wagner, G Zempel, S Broer, J Biber, H Murer, F Lang

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 142 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Roles of Phosphate in Skeleton.Frontiers in endocrinology · 2019
    Review
  6. Phosphate transport: from microperfusion to molecular cloning.Pflugers Archiv : European journal of physiology · 2019
    Article
  7. Review
  8. Article
  9. Vesicular glutamate transporters as anion channels?Pflugers Archiv : European journal of physiology · 2016
    Review
  10. Article
  11. The Concise Guide to PHARMACOLOGY 2013/14: transporters.British journal of pharmacology · 2013
    Article
  12. Article
  13. Article
  14. Vesicular and plasma membrane transporters for neurotransmitters.Cold Spring Harbor perspectives in biology · 2012
    Review
  15. Review
  16. Article
  17. Review
  18. Hereditary disorders of renal phosphate wasting.Nature reviews. Nephrology · 2010
    Review
  19. Article
  20. Article
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

9 authors at 1 institution in 1 country.

A E BuschInstitute of Physiology I, Eberhard-Karls-Universität Tübingen, Germany.
A Schuster
S Waldegger
C A Wagner
G Zempel
S Broer
J Biber
H Murer
F Lang
University of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two distinct molecular types (I and II) of renal proximal tubular brush border Na+/Pi cotransporters have been identified by expression cloning on the basis of their capacity to induce Na+-dependent Pi influx in tracer experiments. Whereas the type II transporters (e.g., NaPi-2 and NaPi-3) resemble well known characteristics of brush border Na+/Pi cotransport, little is known about the properties of the type I transporter (NaPi-1). In contrast to type II, type I transporters produced electrogenic transport only at high extracellular Pi concentrations (> or =3 mM). On the other hand, expression of NaPi-1 induced a Cl- conductance in Xenopus laevis oocytes, which was inhibited by Cl- channel blockers [5-nitro-2-(3-phenylpropylamino)benzoic acid (NPPB) > niflumic acid >> 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid]. Further, the Cl- conductance was inhibited by the organic anions phenol red, benzylpenicillin (penicillin G), and probenecid. These organic anions induced outwardly directed currents in the absence of Cl-. In tracer studies, we observed uptake of benzylpenicillin with a Km of 0.22 mM; benzylpenicillin uptake was inhibited by NPPB and niflumic acid. These findings suggest that the type I Na+/Pi cotransporter functions also as a novel type of anion channel permeable not only for Cl- but also for organic anions. Such an apical anion channel could serve an important role in the transport of Cl- and the excretion of anionic xenobiotics.

Indexed as

Cell Membrane PermeabilitySymportersAnimalsAnionsCarrier ProteinsChloridesFemaleKidney Tubules, ProximalMembrane PotentialsMicrovilliOocytesPatch-Clamp TechniquesPenicillin GPhenolsulfonphthaleinProbenecidRecombinant ProteinsAnionsCarrier ProteinsChloridesPenicillin GPhenolsulfonphthaleinProbenecidRecombinant ProteinsSodium-Phosphate Cotransporter ProteinsSodium-Phosphate Cotransporter Proteins, Type ISodium-Phosphate Cotransporter Proteins, Type IISymporters

Identifiers

PMID8643577
PMCPMC39248
OpenAlexW1964692824

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.