524 research outputs found
Inhibition of I kappa B Kinase Attenuates the Organ Injury and Dysfunction Associated with Hemorrhagic Shock
R Sordi is supported by the program Science without Borders, CAPES Foundation,
Ministry of Education of Brazil, Brasilia/DF, Brazil; NSA Patel is, in part, supported by the Bart’s and The LondonCharity (753/1722). The research leading
to these results has received funding from the People Programme (Marie
Curie Actions) of the European Union′s Seventh Framework Programme
(FP7/2007-2013) under REA grant agreement n° 608765, from the William Harvey
Research Foundation and University of Turin (Ricerca Locale ex-60%). This
work contributes to the Organ Protection
research theme of the Barts Centre
for Trauma Sciences, supported by the
Barts and The London Charity (Award
753/1722) and forms part of the research
themes contributing to the translational
research portfolio of Barts and the London
Cardiovascular Biomedical Research
Unit, which is supported and funded by
the National Institute of Health Researc
Impact of mechanical power and positive end expiratory pressure on central vs. mixed oxygen and carbon dioxide related variables in a population of female piglets
Circadian and Feeding Rhythms Orchestrate the Diurnal Liver Acetylome.
Lysine acetylation is involved in various biological processes and is considered a key reversible post-translational modification in the regulation of gene expression, enzyme activity, and subcellular localization. This post-translational modification is therefore highly relevant in the context of circadian biology, but its characterization on the proteome-wide scale and its circadian clock dependence are still poorly described. Here, we provide a comprehensive and rhythmic acetylome map of the mouse liver. Rhythmic acetylated proteins showed subcellular localization-specific phases that correlated with the related metabolites in the regulated pathways. Mitochondrial proteins were over-represented among the rhythmically acetylated proteins and were highly correlated with SIRT3-dependent deacetylation. SIRT3 activity being nicotinamide adenine dinucleotide (NAD) <sup>+</sup> level-dependent, we show that NAD <sup>+</sup> is orchestrated by both feeding rhythms and the circadian clock through the NAD <sup>+</sup> salvage pathway but also via the nicotinamide riboside pathway. Hence, the diurnal acetylome relies on a functional circadian clock and affects important diurnal metabolic pathways in the mouse liver
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