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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Early, JO; Menon, D; Wyse, CA; Cervantes-Silva, MP; Zaslona, Z; Carroll, RG; Palsson-McDermott, EM; Angiari, S; Ryan, DG; Corcoran, SE; Timmons, G; Geiger, SS; Fitzpatrick, DJ; O'Connell, D; Xavier, RJ; Hokamp, K; O'Neill, LAJ; Curtis, AM.
Circadian clock protein BMAL1 regulates IL-1β in macrophages via NRF2.
Proc Natl Acad Sci U S A. 2018; 115(36): E8460-E8468. Doi: 10.1073/pnas.1800431115 [OPEN ACCESS]
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Co-Autor*innen der Med Uni Graz
Angiari Stefano
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Abstract:
A variety of innate immune responses and functions are dependent on time of day, and many inflammatory conditions are associated with dysfunctional molecular clocks within immune cells. However, the functional importance of these innate immune clocks has yet to be fully characterized. NRF2 plays a critical role in the innate immune system, limiting inflammation via reactive oxygen species (ROS) suppression and direct repression of the proinflammatory cytokines, IL-1β and IL-6. Here we reveal that the core molecular clock protein, BMAL1, controls the mRNA expression of Nrf2 via direct E-box binding to its promoter to regulate its activity. Deletion of Bmal1 decreased the response of NRF2 to LPS challenge, resulting in a blunted antioxidant response and reduced synthesis of glutathione. ROS accumulation was increased in Bmal1 -/- macrophages, facilitating accumulation of the hypoxic response protein, HIF-1α. Increased ROS and HIF-1α levels, as well as decreased activity of NRF2 in cells lacking BMAL1, resulted in increased production of the proinflammatory cytokine, IL-1β. The excessive prooxidant and proinflammatory phenotype of Bmal1 -/- macrophages was rescued by genetic and pharmacological activation of NRF2, or through addition of antioxidants. Our findings uncover a clear role for the molecular clock in regulating NRF2 in innate immune cells to control the inflammatory response. These findings provide insights into the pathology of inflammatory conditions, in which the molecular clock, oxidative stress, and IL-1β are known to play a role. Copyright © 2018 the Author(s). Published by PNAS.
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ARNTL Transcription Factors - genetics
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Animals -
HEK293 Cells -
Humans -
Hypoxia-Inducible Factor 1, alpha Subunit - genetics
Hypoxia-Inducible Factor 1, alpha Subunit - metabolism
Inflammation - chemically induced
Inflammation - genetics
Inflammation - metabolism
Interleukin-1beta - genetics
Interleukin-1beta - metabolism
Lipopolysaccharides - toxicity
Macrophages - metabolism
Macrophages - pathology
Mice -
Mice, Knockout -
NF-E2-Related Factor 2 - genetics
NF-E2-Related Factor 2 - metabolism
Oxidative Stress -
Reactive Oxygen Species - metabolism

Find related publications in this database (Keywords)
circadian clock
BMAL1
oxidative stress
inflammation
macrophage
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