UMP-CMP kinase 2 gene expression in macrophages is dependent on the IRF3-IFNAR signaling axis

• Published in: PloS one Vol. 16; no. 10; p. e0258989
• Main Authors: Kim, Hera, Subbannayya, Yashwanth, Humphries, Fiachra, Skejsol, Astrid, Pinto, Sneha M., Giambelluca, Miriam, Espevik, Terje, Fitzgerald, Katherine A., Kandasamy, Richard K.
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 27.10.2021; Public Library of Science (PLoS)
• Subjects: Analysis; Animals; Antibodies; Antiinfectives and antibacterials; Antiviral agents; Antiviral drugs; Automation; Bacteria; Biological response modifiers; Biology and Life Sciences; Cell activation; Confocal microscopy; CTP; Cytidine triphosphate; Cytoplasm; Fractionation; Gene expression; Gene Expression - immunology; Genes; Genetic aspects; Humans; Immune response; Immune system; Inflammation; Innate immunity; Interferon; Interferon regulatory factor 3; Interferon Regulatory Factor-3 - immunology; Kinases; Ligands; Lipopolysaccharides; Localization; Macrophages; Macrophages - cytology; Macrophages - metabolism; Medicine; Medicine and Health Sciences; Mice; Mice, Knockout; Mitochondria; Nucleic acids; Nucleoside-Phosphate Kinase - immunology; Pathogens; Pattern recognition; Pattern recognition receptors; Polyinosinic:polycytidylic acid; Proteins; Receptor, Interferon alpha-beta - immunology; Receptors; Ribonucleic acid; RNA; Signaling; THP-1 Cells; TLR3 protein; TLR4 protein; Toll-like receptors; Uridine kinase; Viruses; United States; United States > US; Norway; Germany
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0258989

Toll-like receptors (TLRs) are highly-conserved pattern recognition receptors that mediate innate immune responses to invading pathogens and endogenous danger signals released from damaged and dying cells. Activation of TLRs trigger downstream signaling cascades, that culminate in the activation of interferon regulatory factors (IRFs), which subsequently leads to type I interferon (IFN) response. In the current study, we sought to expand the scope of gene expression changes in THP1-derived macrophages upon TLR4 activation and to identify interferon-stimulated genes. RNA-seq analysis led to the identification of several known and novel differentially expressed genes, including CMPK2, particularly in association with type I IFN signaling. We performed an in-depth characterization of CMPK2 expression, a nucleoside monophosphate kinase that supplies intracellular UTP/CTP for nucleic acid synthesis in response to type I IFN signaling in macrophages. CMPK2 was significantly induced at both RNA and protein levels upon stimulation with TLR4 ligand—LPS and TLR3 ligand—Poly (I:C). Confocal microscopy and subcellular fractionation indicated CMPK2 localization in both cytoplasm and mitochondria of THP-1 macrophages. Furthermore, neutralizing antibody-based inhibition of IFNAR receptor in THP-1 cells and BMDMs derived from IFNAR KO and IRF3 KO knockout mice further revealed that CMPK2 expression is dependent on LPS/Poly (I:C) mediated IRF3- type I interferon signaling. In summary, our findings suggest that CMPK2 is a potential interferon-stimulated gene in THP-1 macrophages and that CMPK2 may facilitate IRF3- type I IFN-dependent anti-bacterial and anti-viral roles.