Evidence map›Paper›PMID 20962000›Full record

ArticleThe Journal of physiology2010

Hydrogen ion dynamics in human red blood cells.

Pawel Swietach, Teresa Tiffert, Jakob M A Mauritz, Rachel Seear, Alessandro Esposito, Clemens F Kaminski, Virgilio L Lew, Richard D Vaughan-Jones

Abstract read
In one paragraph

Article in The Journal of physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
–field-weighted citation impact
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

36 citing papers in PubMed.

  1. Soluble adenylyl cyclase in nonmammalian sperm is directly controlled by pH, not by HCOProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Loss of NaActa physiologica (Oxford, England) · 2025
    Article
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  9. Chloride Gradient Is Involved in Ammonium Influx in Human Erythrocytes.International journal of molecular sciences · 2024
    Article
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  18. Single-cell OProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  19. Review
  20. The solute carrier SLC9C1 is a NaNature communications · 2018
    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

8 authors.

Pawel SwietachDepartment of Physiology, Burdon Sanderson Cardiac Science Centre, Parks Road, Oxford OX1 3PT, UK. pawel.swietach@dpag.ox.ac.uk
Teresa Tiffert
Jakob M A Mauritz
Rachel Seear
Alessandro Esposito
Clemens F Kaminski
Virgilio L Lew
Richard D Vaughan-Jones

Funding

Biotechnology and Biological Sciences Research Council BB/E008542/1British Heart Foundation RG/08/016/26423Medical Research Council G0700698Medical Research Council MC_G1000734Wellcome Trust 089703
6 · The paper itself

Abstract

Our understanding of pH regulation within red blood cells (RBCs) has been inferred mainly from indirect experiments rather than from in situ measurements of intracellular pH (pH(i)). The present work shows that carboxy-SNARF-1, a pH fluorophore, when used with confocal imaging or flow cytometry, reliably reports pH(i) in individual, human RBCs, provided intracellular fluorescence is calibrated using a 'null-point' procedure. Mean pH(i) was 7.25 in CO(2)/HCO(3)(-)-buffered medium and 7.15 in Hepes-buffered medium, and varied linearly with extracellular pH (slope of 0.77). Intrinsic (non-CO(2)/HCO(3)(-)-dependent) buffering power, estimated in the intact cell (85 mmol (l cell)(-1) (pH unit)(-1) at resting pH(i)), was somewhat higher than previous estimates from cell lysates (50-70 mmol (l cell)(-1) (pH unit)(-1)). Acute displacement of pH(i) (superfusion of weak acids/bases) triggered rapid pH(i) recovery. This was mediated via membrane Cl(-)/HCO(3)(-) exchange (the AE1 gene product), irrespective of whether recovery was from an intracellular acid or base load, and with no evident contribution from other transporters such as Na(+)/H(+) exchange. H(+)-equivalent flux through AE1 was a linear function of [H(+)](i) and reversed at resting pH(i), indicating that its activity is not allosterically regulated by pH(i), in contrast to other AE isoforms. By simultaneously monitoring pH(i) and markers of cell volume, a functional link between membrane ion transport, volume and pH(i) was demonstrated. RBC pH(i) is therefore tightly regulated via AE1 activity, but modulated during changes of cell volume. A comparable volume-pH(i) link may also be important in other cell types expressing anion exchangers. Direct measurement of pH(i) should be useful in future investigations of RBC physiology and pathology.

Indexed as

ProtonsAnion Exchange Protein 1, ErythrocyteBenzopyransBicarbonatesBuffersCarbon DioxideChloridesErythrocytesFluorescenceHumansHydrogen-Ion ConcentrationNaphtholsRhodaminesAnion Exchange Protein 1, ErythrocyteBenzopyransBicarbonatesBuffersCarbon DioxideChloridesNaphtholsProtonsRhodaminesseminaphthorhodaminefluoride

Identifiers

PMID20962000
PMCPMC3036193

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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.