Evidence map›Paper›PMID 17317744›Full record

ArticleThe Journal of physiology2007

A conductive pathway generated from fragments of the human red cell anion exchanger AE1.

Mark D Parker, Mark T Young, Christopher M Daly, Robert W Meech, Walter F Boron, Michael J A Tanner

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. A novel mutant NaThe Journal of physiology · 2016
    Article
  3. Article
  4. Review
  5. Pendrin function and regulation in Xenopus oocytes.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2011
    Article
  6. Article
  7. Cloning and characterization of a zebrafish homologue of human AQP1: a bifunctional water and gas channel.American journal of physiology. Regulatory, integrative and comparative physiology · 2010
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review. Leaky Cl--HCO3- exchangers: cation fluxes via modified AE1.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2009
    Review
  13. Article
  14. 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

6 authors at 2 institutions in 2 countries.

Mark D ParkerDepartment of Biochemistry, University of Bristol, University Walk, Bristol, BS8 1TD, UK. mark.parker@yale.edu
Mark T Young
Christopher M Daly
Robert W Meech
Walter F Boron
Michael J A Tanner
Yale University · USUniversity of Bristol · GB

Funding

PH REGULATION OF EXCITABLE INVERTEBRATE CELLSR01NS018400 · NINDS · YALE UNIVERSITY · PI BORON, WALTER F · 1985 to 2012
$5.1M
Physiology of Electrogenic Na/HCO3 CotransportersR37DK030344 · NIDDK · YALE UNIVERSITY · PI BORON, WALTER F · 2002 to 2011
$3.5M
NIDDK NIH HHS R37 DK030344NINDS NIH HHS NS18400NINDS NIH HHS R01 NS018400PHS HHS P30-34989Wellcome Trust
6 · The paper itself

Abstract

Human red cell anion exchanger AE1 (band 3) is an electroneutral Cl-HCO3- exchanger with 12-14 transmembrane spans (TMs). Previous work using Xenopus oocytes has shown that two co-expressed fragments of AE1 lacking TMs 6 and 7 are capable of forming a stilbene disulphonate-sensitive (36)Cl-influx pathway, reminiscent of intact AE1. In the present study, we create a single construct, AE1Delta(6: 7), representing the intact protein lacking TMs 6 and 7. We expressed this construct in Xenopus oocytes and evaluated it employing a combination of two-electrode voltage clamp and pH-sensitive microelectrodes. We found that, whereas AE1Delta(6: 7) has some electroneutral Cl-base exchange activity, the protein also forms a novel anion-conductive pathway that is blocked by DIDS. The mutation Lys(539)Ala at the covalent DIDS-reaction site of AE1 reduced the DIDS sensitivity, demonstrating that (1) the conductive pathway is intrinsic to AE1Delta(6: 7) and (2) the conductive pathway has some commonality with the electroneutral anion-exchange pathway. The conductance has an anion-permeability sequence: NO3- approximately I- > NO2- > Br- > Cl- > SO4(2-) approximately HCO3- approximately gluconate- approximately aspartate- approximately cyclamate-. It may also have a limited permeability to Na+ and the zwitterion taurine. Although this conductive pathway is not a usual feature of intact mammalian AE1, it shares many properties with the anion-conductive pathways intrinsic to two other Cl-HCO3- exchangers, trout AE1 and mammalian SLC26A7.

Indexed as

4,4'-Diisothiocyanostilbene-2,2'-Disulfonic AcidAmino Acid Transport Systems, NeutralAnimalsAnion Exchange Protein 1, ErythrocyteChloride-Bicarbonate AntiportersElectrophysiologyFemaleGene Expression RegulationHumansHydrogen-Ion ConcentrationMutationOocytesPatch-Clamp TechniquesPeptide FragmentsSignal TransductionTaurine4,4'-Diisothiocyanostilbene-2,2'-Disulfonic AcidAmino Acid Transport Systems, NeutralAnion Exchange Protein 1, ErythrocyteChloride-Bicarbonate AntiportersPeptide FragmentsTaurine

Identifiers

PMID17317744
PMCPMC2075216
OpenAlexW2156501109

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.