HIF1A and NFAT5 coordinate Na+-boosted antibacterial defense via enhanced autophagy and autolysosomal targeting

Autor: Patrick Neubert, Jonathan Jantsch, Christoph Brochhausen, Dominik N. Müller, John R. Ferdinand, Karin Hammer, Jens Titze, Ger van Zandbergen, Michaela Simon, Menna R. Clatworthy, Stefan Wagner, Katrina J. Binger, Valentin Schatz, Carmen Reitinger, Roman G. Gerlach, Christian Kurts, Agnes Schröder, Andrea Weichselbaum, Anna-Lorena Bär, Stefan Tomiuk, Kento Kitada, Zeinab Abdullah
Přispěvatelé: Ferdinand, John [0000-0003-0936-0128], Clatworthy, Menna [0000-0002-3340-9828], Apollo - University of Cambridge Repository
Rok vydání: 2019
Předmět:
0301 basic medicine
Nitric Oxide Synthase Type II
macrophage
Cathepsin B
ATG12
03 medical and health sciences
Mice
Sequestosome 1
Microscopy
Electron
Transmission

Osmotic Pressure
Autophagy
Escherichia coli
salt
Animals
Mannitol
ddc:610
Phosphoglycerate kinase 1
education
Molecular Biology
Protein kinase B
Mechanistic target of rapamycin
sodium
Oligonucleotide Array Sequence Analysis
Homeodomain Proteins
Inflammation
education.field_of_study
030102 biochemistry & molecular biology
biology
Macrophages
TOR Serine-Threonine Kinases
Sodium
E. coli
Autophagosomes
Nitric oxide synthase 2
Cell Biology
BECN1
Hydrogen-Ion Concentration
Hypoxia-Inducible Factor 1
alpha Subunit

Molecular biology
030104 developmental biology
biology.protein
cell-autonomous immunity
610 Medizin und Gesundheit
Lysosomes
Reactive Oxygen Species
Proto-Oncogene Proteins c-akt
Transcription Factors
DOI: 10.6084/m9.figshare.7992203
Popis: Infection and inflammation are able to induce diet-independent Na+-accumulation without commensurate water retention in afflicted tissues, which favors the pro-inflammatory activation of mouse macrophages and augments their antibacterial and antiparasitic activity. While Na+-boosted host defense against the protozoan parasite Leishmania major is mediated by increased expression of the leishmanicidal NOS2 (nitric oxide synthase 2, inducible), the molecular mechanisms underpinning this enhanced antibacterial defense of mouse macrophages with high Na+ (HS) exposure are unknown. Here, we provide evidence that HS-increased antibacterial activity against E. coli was neither dependent on NOS2 nor on the phagocyte oxidase. In contrast, HS-augmented antibacterial defense hinged on HIF1A (hypoxia inducible factor 1, alpha subunit)-dependent increased autophagy, and NFAT5 (nuclear factor of activated T cells 5)-dependent targeting of intracellular E. coli to acidic autolysosomal compartments. Overall, these findings suggest that the autolysosomal compartment is a novel target of Na+-modulated cell autonomous innate immunity. Abbreviations: ACT: actins; AKT: AKT serine/threonine kinase 1; ATG2A: autophagy related 2A; ATG4C: autophagy related 4C, cysteine peptidase; ATG7: autophagy related 7; ATG12: autophagy related 12; BECN1: beclin 1; BMDM: bone marrow-derived macrophages; BNIP3: BCL2/adenovirus E1B interacting protein 3; CFU: colony forming units; CM-H2DCFDA: 5-(and-6)-chloromethyl-2′,7′-dichlorodihydrofluorescein diacetate, acetyl ester; CTSB: cathepsin B; CYBB: cytochrome b-245 beta chain; DAPI: 4,6-diamidino-2-phenylindole; DMOG: dimethyloxallyl glycine; DPI: diphenyleneiodonium chloride; E. coli: Escherichia coli; FDR: false discovery rate; GFP: green fluorescent protein; GSEA: gene set enrichment analysis; GO: gene ontology; HIF1A: hypoxia inducible factor 1, alpha subunit; HUGO: human genome organization; HS: high salt (+ 40 mM of NaCl to standard cell culture conditions); HSP90: heat shock 90 kDa proteins; LDH: lactate dehydrogenase; LPS: lipopolysaccharide; Lyz2/LysM: lysozyme 2; NFAT5/TonEBP: nuclear factor of activated T cells 5; MΦ: macrophages; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MFI: mean fluorescence intensity; MIC: minimum inhibitory concentration; MOI: multiplicity of infection; MTOR: mechanistic target of rapamycin kinase; NaCl: sodium chloride; NES: normalized enrichment score; n.s.: not significant; NO: nitric oxide; NOS2/iNOS: nitric oxide synthase 2, inducible; NS: normal salt; PCR: polymerase chain reaction; PGK1: phosphoglycerate kinase 1; PHOX: phagocyte oxidase; RFP: red fluorescent protein; RNA: ribonucleic acid; ROS: reactive oxygen species; sCFP3A: super cyan fluorescent protein 3A; SBFI: sodium-binding benzofuran isophthalate; SLC2A1/GLUT1: solute carrier family 2 (facilitated glucose transporter), member 1; SQSTM1/p62: sequestosome 1; ULK1: unc-51 like kinase 1; v-ATPase: vacuolar-type H+-ATPase; WT: wild type
Databáze: OpenAIRE