Frontiers in Immunology · 2018 · 28 citations · 49 references
Life SciencesImmunologyPharmacologyHost-pathogen InteractionsInflammationInnate ImmunityBacterial PathogenesisCytokine BiologyInflammation In Infectious DiseaseInnate Immune ResponseInnate Immune Signaling PathwaysMacrophage BiologyAntibacterial ImmunityAntimicrobial ImmunityHistone DeacetylasesHost Defense Against Bacterial InfectionInnate Immune FunctionInnate Immunity PathwaysMacrophage Cytokine ProductionOxidative Stress Response Pathways
Sirtuin 5 (SIRT5) is a member of the family of NAD+-dependent lysine/histone deacetylases. SIRT5 resides mainly in the mitochondria where it catalyses deacetylation, demalonylation, desuccinylation and deglutarylation of lysine to regulate metabolic and oxidative stress response pathways. Pharmacologic inhibitors of SIRT5 are under development for oncologic conditions, but nothing is known about the impact of SIRT5 on antimicrobial innate immune defenses. Using SIRT5 knockout mice, we show that SIRT5 deficiency does not affect immune cell development, cytokine production and proliferation by macrophages and splenocytes exposed to microbial and immunological stimuli. Moreover, preclinical models suggest that SIRT5 deficiency does not worsen endotoxemia, Klebsiella pneumoniae and Streptococcus pneumoniae pneumonia, Escherichia coli peritonitis, listeriosis and staphylococcal infection. Altogether, these data support the safety profile in terms of susceptibility to infections of SIRT5 inhibitors under development.
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Genomic Instability and Aging-like Phenotype in the Absence of Mammalian SIRT6
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Sirt5 Is a NAD-Dependent Protein Lysine Demalonylase and Desuccinylase
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SIRT5-Mediated Lysine Desuccinylation Impacts Diverse Metabolic Pathways
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Lysine Glutarylation Is a Protein Posttranslational Modification Regulated by SIRT5
Minjia Tan, Chao Peng, Kristin A. Anderson et al. · Cell Metabolism · 2014 · 882 citations · Full text