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Mechanisms and physiological function of daily haemoglobin oxidation rhythms in red blood cells
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 h...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548169/ https://www.ncbi.nlm.nih.gov/pubmed/37554073 http://dx.doi.org/10.15252/embj.2023114164 |
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author | Beale, Andrew D Hayter, Edward A Crosby, Priya Valekunja, Utham K Edgar, Rachel S Chesham, Johanna E Maywood, Elizabeth S Labeed, Fatima H Reddy, Akhilesh B Wright, Kenneth P Lilley, Kathryn S Bechtold, David A Hastings, Michael H O'Neill, John S |
author_facet | Beale, Andrew D Hayter, Edward A Crosby, Priya Valekunja, Utham K Edgar, Rachel S Chesham, Johanna E Maywood, Elizabeth S Labeed, Fatima H Reddy, Akhilesh B Wright, Kenneth P Lilley, Kathryn S Bechtold, David A Hastings, Michael H O'Neill, John S |
author_sort | Beale, Andrew D |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10548169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105481692023-10-05 Mechanisms and physiological function of daily haemoglobin oxidation rhythms in red blood cells Beale, Andrew D Hayter, Edward A Crosby, Priya Valekunja, Utham K Edgar, Rachel S Chesham, Johanna E Maywood, Elizabeth S Labeed, Fatima H Reddy, Akhilesh B Wright, Kenneth P Lilley, Kathryn S Bechtold, David A Hastings, Michael H O'Neill, John S EMBO J Articles 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. John Wiley and Sons Inc. 2023-08-09 /pmc/articles/PMC10548169/ /pubmed/37554073 http://dx.doi.org/10.15252/embj.2023114164 Text en © 2023 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Beale, Andrew D Hayter, Edward A Crosby, Priya Valekunja, Utham K Edgar, Rachel S Chesham, Johanna E Maywood, Elizabeth S Labeed, Fatima H Reddy, Akhilesh B Wright, Kenneth P Lilley, Kathryn S Bechtold, David A Hastings, Michael H O'Neill, John S Mechanisms and physiological function of daily haemoglobin oxidation rhythms in red blood cells |
title | Mechanisms and physiological function of daily haemoglobin oxidation rhythms in red blood cells |
title_full | Mechanisms and physiological function of daily haemoglobin oxidation rhythms in red blood cells |
title_fullStr | Mechanisms and physiological function of daily haemoglobin oxidation rhythms in red blood cells |
title_full_unstemmed | Mechanisms and physiological function of daily haemoglobin oxidation rhythms in red blood cells |
title_short | Mechanisms and physiological function of daily haemoglobin oxidation rhythms in red blood cells |
title_sort | mechanisms and physiological function of daily haemoglobin oxidation rhythms in red blood cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548169/ https://www.ncbi.nlm.nih.gov/pubmed/37554073 http://dx.doi.org/10.15252/embj.2023114164 |
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