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bioRxiv · 10.1101/2021.10.11.463714

Clock gene-independent daily regulation of haemoglobin oxidation in red blood cells

Beale, A. D.·Crosby, P.·Valekunja, U. K.·Edgar, R. S.·Chesham, J. E.·Maywood, E. S.·Labeed, F. H.·Reddy, A. B.·Wright, K. P.·Lilley, K. S.·Hastings, M. H.·O'Neill, J. S.
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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 RBCs cultured in vitro or taken from freely behaving mice or humans exhibit 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 NO signaling. These results extend our molecular understanding of RBC circadian rhythms and suggest they contribute to the regulation of body temperature.

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Beale, A. D., Crosby, P., Valekunja, U. K., Edgar, R. S., Chesham, J. E., Maywood, E. S., Labeed, F. H., Reddy, A. B., Wright, K. P., Lilley, K. S., Hastings, M. H., O'Neill, J. S.. 2021-10-11. Clock gene-independent daily regulation of haemoglobin oxidation in red blood cells. https://doi.org/10.1101/2021.10.11.463714

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