Evidence map›Paper›PMID 37554073›Full record

ArticleThe EMBO journal2023

Mechanisms and physiological function of daily haemoglobin oxidation rhythms in red blood cells.

Andrew D Beale, Edward A Hayter, Priya Crosby, Utham K Valekunja, Rachel S Edgar, Johanna E Chesham, Elizabeth S Maywood, Fatima H Labeed, Akhilesh B Reddy, Kenneth P Wright and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

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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

14 authors at 7 institutions in 2 countries.

Andrew D BealeMRC Laboratory of Molecular Biology, Cambridge, UK.ORCID 0000-0002-2051-0919
Edward A HayterCentre for Biological Timing, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID 0000-0001-9996-7198
Priya CrosbyMRC Laboratory of Molecular Biology, Cambridge, UK.ORCID 0000-0002-7532-7708
Utham K ValekunjaDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0003-2385-4239
Rachel S EdgarDepartment of Infectious Diseases, Imperial College London, London, UK.ORCID 0000-0002-3348-0851
Johanna E CheshamMRC Laboratory of Molecular Biology, Cambridge, UK.ORCID 0000-0002-8981-2667
Elizabeth S MaywoodMRC Laboratory of Molecular Biology, Cambridge, UK.ORCID 0000-0002-4557-9955
Fatima H LabeedFaculty of Engineering and Physical Sciences, University of Surrey, Guildford, UK.ORCID 0000-0002-0092-257X
Akhilesh B ReddyDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0003-3328-1470
Kenneth P WrightDepartment of Integrative Physiology, Sleep and Chronobiology Laboratory, University of Colorado Boulder, Boulder, CO, USA.ORCID 0000-0002-1781-7469
Kathryn S LilleyCambridge Centre for Proteomics, Department of Biochemistry, University of Cambridge, Cambridge, UK.ORCID 0000-0003-0594-6543
David A BechtoldCentre for Biological Timing, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID 0000-0001-8676-8704
Michael H HastingsMRC Laboratory of Molecular Biology, Cambridge, UK.ORCID 0000-0001-8576-6651
John S O'NeillMRC Laboratory of Molecular Biology, Cambridge, UK.ORCID 0000-0003-2204-6096
MRC Laboratory of Molecular Biology · GBManchester Academic Health Science Centre · GBTranslational Therapeutics (United States) · USImperial College London · GBUniversity of Cambridge · GBUniversity of Colorado Boulder · USUniversity of Surrey · GB

Funding

Determination of the mechanistic targets of metforminDP1DK126167 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI REDDY, AKHILESH BASI · 2020 to 2024
$3.9M
Mechanistic Basis of Circadian Clocks in Bmal1 Knockout MiceR01GM139211 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI REDDY, AKHILESH BASI · 2021 to 2024
$2.1M
Biotechnology and Biological Sciences Research Council BB/V002651/1Medical Research Council MC_U105170643Medical Research Council MC_UP_1201/4Medical Research Council MR/P00279X/1NIDDK NIH HHS DP1 DK126167NIGMS NIH HHS R01 GM139211Wellcome TrustWellcome Trust 093734/Z/10/ZWellcome Trust 100333/Z/12/Z
6 · The paper itself

Abstract

Cellular circadian rhythms confer temporal organisation upon physiology that is fundamental to human health. Rhythms are present in red blood cells (RBCs), the most abundant cell type in the body, but their physiological function is poorly understood. Here, we present a novel biochemical assay for haemoglobin (Hb) oxidation status which relies on a redox-sensitive covalent haem-Hb linkage that forms during SDS-mediated cell lysis. Formation of this linkage is lowest when ferrous Hb is oxidised, in the form of ferric metHb. Daily haemoglobin oxidation rhythms are observed in mouse and human RBCs cultured in vitro, or taken from humans in vivo, and are unaffected by mutations that affect circadian rhythms in nucleated cells. These rhythms correlate with daily rhythms in core body temperature, with temperature lowest when metHb levels are highest. Raising metHb levels with dietary sodium nitrite can further decrease daytime core body temperature in mice via nitric oxide (NO) signalling. These results extend our molecular understanding of RBC circadian rhythms and suggest they contribute to the regulation of body temperature.

Indexed as

ErythrocytesHemoglobinsAnimalsCircadian RhythmHemeHumansMiceOxidation-ReductionHemeHemoglobinsbody temperaturecircadian rhythmserythrocytehaemoglobinredox

Identifiers

PMID37554073
PMCPMC10548169
OpenAlexW4385683564

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.