Evidence map›Paper›PMID 15929723›Full record

ArticleThe Biochemical journal2005

Human Rhesus B and Rhesus C glycoproteins: properties of facilitated ammonium transport in recombinant kidney cells.

Nedjma Zidi-Yahiaoui, Isabelle Mouro-Chanteloup, Anne-Marie D'Ambrosio, Claude Lopez, Pierre Gane, Caroline Le van Kim, Jean-Pierre Cartron, Yves Colin, Pierre Ripoche

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

41 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
  2. Rhbg interaction with CA-IV and its effects on NHAmerican journal of physiology. Cell physiology · 2025
    Article
  3. Ammonia transporter RhBG initiates downstream signaling and functional responses by activating NFκB.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Mechanisms of ammonia and ammonium transport by rhesus-associated glycoproteins.American journal of physiology. Cell physiology · 2015
    Article
  9. Renal acid-base regulation: new insights from animal models.Pflugers Archiv : European journal of physiology · 2015
    Review
  10. Article
  11. Article
  12. Article
  13. Ammonia transport in the kidney by Rhesus glycoproteins.American journal of physiology. Renal physiology · 2014
    Review
  14. Article
  15. Article
  16. Renal ammonia metabolism and transport.Comprehensive Physiology · 2013
    Review
  17. Article
  18. Article
  19. Role of NH3 and NH4+ transporters in renal acid-base transport.American journal of physiology. Renal physiology · 2011
    Review
  20. pH sensitivity of ammonium transport by Rhbg.American journal of physiology. Cell physiology · 2010
    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 3 institutions in 1 country.

Nedjma Zidi-YahiaouiINSERM, U665, Paris, F-75015, France.
Isabelle Mouro-Chanteloup
Anne-Marie D'Ambrosio
Claude Lopez
Pierre Gane
Caroline Le van Kim
Jean-Pierre Cartron
Yves Colin
Pierre Ripoche
Inserm · FRInstitut National de la Transfusion Sanguine · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mammalian Rh (Rhesus) protein family belongs to the Amt/Mep (ammonia transporter/methylammonium permease)/Rh superfamily of ammonium transporters. Whereas RhCE, RhD and RhAG are erythroid specific, RhBG and RhCG are expressed in key organs associated with ammonium transport and metabolism. We have investigated the ammonium transport function of human RhBG and RhCG by comparing intracellular pH variation in wild-type and transfected HEK-293 (human embryonic kidney) cells and MDCK (Madin-Darby canine kidney) cells in the presence of ammonium (NH4+/NH3) gradients. Stopped-flow spectrofluorimetry analysis, using BCECF [2',7'-bis-(2-carboxyethyl)-5(6)-carboxyfluorescein] as a pH-sensitive probe, revealed that all cells submitted to inwardly or outwardly directed ammonium gradients exhibited rapid alkalinization or acidification phases respectively, which account for ammonium movements in transfected and native cells. However, as compared with wild-type cells known to have high NH3 lipid permeability, RhBG- and RhCG-expressing cells exhibited ammonium transport characterized by: (i) a five to six times greater kinetic rate-constant; (ii) a weak temperature-dependence; and (iii) reversible inhibition by mercuric chloride (IC50: 52 microM). Similarly, when subjected to a methylammonium gradient, RhBG- and RhCG-expressing cells exhibited kinetic rate constants greater than those of native cells. However, these constants were five times higher for RhBG as compared with RhCG, suggesting a difference in substrate accessibility. These results, indicating that RhBG and RhCG facilitate rapid and low-energy-dependent bi-directional ammonium movement across the plasma membrane, favour the hypothesis that these Rh glycoproteins, together with their erythroid homologue RhAG [Ripoche, Bertrand, Gane, Birkenmeier, Colin and Cartron (2005) Proc. Natl. Acad. Sci. U.S.A. 101, 17222-17227] constitute a family of NH3 channels in mammalian cells.

Indexed as

AnimalsBiological TransportCation Transport ProteinsCell LineCell MembraneCell Membrane PermeabilityDogsFlow CytometryGlycoproteinsHumansHydrogen-Ion ConcentrationKidneyKineticsMembrane GlycoproteinsMembrane Transport ProteinsMercuric ChlorideCation Transport ProteinsGlycoproteinsMembrane GlycoproteinsMembrane Transport ProteinsMercuric ChloridemethylamineMethylaminesQuaternary Ammonium CompoundsRHBG protein, humanRHCG protein, human

Identifiers

PMID15929723
PMCPMC1237136
OpenAlexW2001619223

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.