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Dim Light at Night Impairs Daily Variation of Circulating Immune Cells and Renal Immune Homeostasis

Dim light at night (dLAN) has become a pervasive part of the modern world, and growing evidence shows its association with increased health risks. Though this link is attributed to a disturbed circadian clock, the underlying mechanisms that can explain how circadian disruption from dLAN causes negat...

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Autores principales: Okuliarova, Monika, Mazgutova, Nikoleta, Majzunova, Miroslava, Rumanova, Valentina Sophia, Zeman, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862740/
https://www.ncbi.nlm.nih.gov/pubmed/33552079
http://dx.doi.org/10.3389/fimmu.2020.614960
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author Okuliarova, Monika
Mazgutova, Nikoleta
Majzunova, Miroslava
Rumanova, Valentina Sophia
Zeman, Michal
author_facet Okuliarova, Monika
Mazgutova, Nikoleta
Majzunova, Miroslava
Rumanova, Valentina Sophia
Zeman, Michal
author_sort Okuliarova, Monika
collection PubMed
description Dim light at night (dLAN) has become a pervasive part of the modern world, and growing evidence shows its association with increased health risks. Though this link is attributed to a disturbed circadian clock, the underlying mechanisms that can explain how circadian disruption from dLAN causes negative health effects remain unclear. Here, we exposed rats to a light–dark cycle (12:12 h) with low-intensity light at night (~2 lx) for 2 and 5 weeks and explored the steady-state pattern of circulating immune cells and renal immune-related markers, which are well controlled by the circadian clock. After 5 weeks, dLAN impaired the daily variation in several types of white blood cells, especially monocytes and T cells. Two-week dLAN caused a reduction in blood monocytes and altered gene expression of macrophage marker Cd68 and monocyte-attracting chemokine Ccl2 in the kidney. Interestingly, dLAN decreased renal 3-nitrotyrosine levels and resulted in up-regulation of the main endogenous antioxidant pathways, indicating a disturbance in the renal redox balance and an activation of compensatory mechanisms. These effects paralleled the altered renal expression of the molecular clock components and increased plasma corticosterone levels. Together, our results show that chronic exposure to dLAN weakened the circadian control of daily variation of circulating immune cells and disturbed renal immune and redox homeostasis. Consequences of this dLAN-disturbed immune balance on the ability of the immune system to cope with other challenges should by clarified in further studies.
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spelling pubmed-78627402021-02-06 Dim Light at Night Impairs Daily Variation of Circulating Immune Cells and Renal Immune Homeostasis Okuliarova, Monika Mazgutova, Nikoleta Majzunova, Miroslava Rumanova, Valentina Sophia Zeman, Michal Front Immunol Immunology Dim light at night (dLAN) has become a pervasive part of the modern world, and growing evidence shows its association with increased health risks. Though this link is attributed to a disturbed circadian clock, the underlying mechanisms that can explain how circadian disruption from dLAN causes negative health effects remain unclear. Here, we exposed rats to a light–dark cycle (12:12 h) with low-intensity light at night (~2 lx) for 2 and 5 weeks and explored the steady-state pattern of circulating immune cells and renal immune-related markers, which are well controlled by the circadian clock. After 5 weeks, dLAN impaired the daily variation in several types of white blood cells, especially monocytes and T cells. Two-week dLAN caused a reduction in blood monocytes and altered gene expression of macrophage marker Cd68 and monocyte-attracting chemokine Ccl2 in the kidney. Interestingly, dLAN decreased renal 3-nitrotyrosine levels and resulted in up-regulation of the main endogenous antioxidant pathways, indicating a disturbance in the renal redox balance and an activation of compensatory mechanisms. These effects paralleled the altered renal expression of the molecular clock components and increased plasma corticosterone levels. Together, our results show that chronic exposure to dLAN weakened the circadian control of daily variation of circulating immune cells and disturbed renal immune and redox homeostasis. Consequences of this dLAN-disturbed immune balance on the ability of the immune system to cope with other challenges should by clarified in further studies. Frontiers Media S.A. 2021-01-22 /pmc/articles/PMC7862740/ /pubmed/33552079 http://dx.doi.org/10.3389/fimmu.2020.614960 Text en Copyright © 2021 Okuliarova, Mazgutova, Majzunova, Rumanova and Zeman http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Okuliarova, Monika
Mazgutova, Nikoleta
Majzunova, Miroslava
Rumanova, Valentina Sophia
Zeman, Michal
Dim Light at Night Impairs Daily Variation of Circulating Immune Cells and Renal Immune Homeostasis
title Dim Light at Night Impairs Daily Variation of Circulating Immune Cells and Renal Immune Homeostasis
title_full Dim Light at Night Impairs Daily Variation of Circulating Immune Cells and Renal Immune Homeostasis
title_fullStr Dim Light at Night Impairs Daily Variation of Circulating Immune Cells and Renal Immune Homeostasis
title_full_unstemmed Dim Light at Night Impairs Daily Variation of Circulating Immune Cells and Renal Immune Homeostasis
title_short Dim Light at Night Impairs Daily Variation of Circulating Immune Cells and Renal Immune Homeostasis
title_sort dim light at night impairs daily variation of circulating immune cells and renal immune homeostasis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862740/
https://www.ncbi.nlm.nih.gov/pubmed/33552079
http://dx.doi.org/10.3389/fimmu.2020.614960
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