
Journal of Innate Immunity, Journal Year: 2024, Volume and Issue: 16(1), P. 367 - 369
Published: Jan. 1, 2024
Language: Английский
Journal of Innate Immunity, Journal Year: 2024, Volume and Issue: 16(1), P. 367 - 369
Published: Jan. 1, 2024
Language: Английский
Frontiers in Nutrition, Journal Year: 2024, Volume and Issue: 11
Published: Sept. 2, 2024
Very-low-carbohydrate diets, including ketogenic and carnivore are gaining popularity for the experimental treatment of a wide range disorders, inflammatory bowel disease (IBD).
Language: Английский
Citations
9Chinese Journal of Chemistry, Journal Year: 2024, Volume and Issue: 42(18), P. 2187 - 2196
Published: May 14, 2024
Comprehensive Summary Redox nanozymes offer an appealing reactive oxygen species (ROS)‐based antibacterial strategy via disrupting intracellular homeostasis, however, they still face many obstacles such as low enzymic activity and irreversible loss of catalytic active center. Meanwhile, the antioxidant glutathione (GSH) overexpressed in infected sites would limit therapy efficiency. Herein, we develop a multifunctional nanozyme based on copper(I) (Cu + ) ion doped MoO 3– x ‐MoO by simple yet efficient vacancy‐reduced without any pretreatment or additional agents. The resultant Cu hybrid possesses enhanced peroxidase‐like (POD‐like) activity, rapid GSH‐depleting function biodegradable ability. It can achieve highly elimination Pseudomonas aeruginosa ( P. cellular redox balance. More intriguingly, reaction between GSH could translate Mo 6+ into 5+ , thereby leading to partial recovery POD‐like for continuous ∙ OH generation. In vitro vivo experiments demonstrated that had stronger property compared consumption plentiful generation providing extra H 2 O well neglective toxicity healthy organs. view its remarkable good biosafety, developed be used promising antimicrobial infection.
Language: Английский
Citations
7Trends in Endocrinology and Metabolism, Journal Year: 2024, Volume and Issue: 35(3), P. 177 - 179
Published: Jan. 31, 2024
Language: Английский
Citations
4Cell Reports, Journal Year: 2024, Volume and Issue: 43(9), P. 114648 - 114648
Published: Aug. 20, 2024
Metabolic reprogramming is crucial for activating innate immunity in macrophages, and the accumulation of immunometabolites essential effective defense against infection. The NAD
Language: Английский
Citations
4Brain Behavior and Immunity, Journal Year: 2025, Volume and Issue: 125, P. 280 - 291
Published: Jan. 15, 2025
Language: Английский
Citations
0Frontiers in Immunology, Journal Year: 2025, Volume and Issue: 16
Published: April 3, 2025
Pulmonary diseases, arising from infections caused by bacteria, fungi, and viruses, or stemming underlying genetic factors are one of the leading causes mortality in humans, accounting for millions deaths every year. At onset pulmonary crucial roles played phagocytic immune cells, particularly tissue-resident macrophages, regulating response at mucosal barrier. Recent strides have illuminated pivotal role host bioenergetics modulated metabolites derived both pathogens hosts influencing pathophysiology major organs. Their influence extends to processes such as infiltration activation polarization phenomenon. Furthermore, host-derived metabolites, itaconate, contribute promotion anti-inflammatory responses, thereby preventing immunopathology facilitating preservation niches thrive long-term. This review explores recent advancements field immunometabolism, with a particular emphasis on intricacies disease progression bacteria P. aeruginosa, M. tuberculosis S. aureus fungi like C. albicans.
Language: Английский
Citations
0Current Opinion in Microbiology, Journal Year: 2025, Volume and Issue: 85, P. 102608 - 102608
Published: April 4, 2025
Language: Английский
Citations
0Elsevier eBooks, Journal Year: 2025, Volume and Issue: unknown, P. 7 - 26
Published: Jan. 1, 2025
Language: Английский
Citations
0Nature Communications, Journal Year: 2025, Volume and Issue: 16(1)
Published: April 19, 2025
Disease tolerance mitigates organ damage from non-resolving inflammation during persistent infections, yet its underlying mechanisms remain unclear. Here we show, in a Pseudomonas aeruginosa pneumonia mouse model, that disease depends on the mitochondrial metabolite itaconate, which mediates cooperative host-pathogen interactions. In P. aeruginosa, itaconate modifies key cysteine residues TCA cycle enzymes critical for succinate metabolism, inducing bioenergetic stress and promoting formation biofilms are less immunostimulatory allow bacteria to integrate into local microbiome. Itaconate incorporates central metabolism of biofilm, driving exopolysaccharide production-particularly alginate-which amplifies airway signaling. This itaconate-alginate interplay limits host immunopathology by enabling pulmonary glutamine assimilation, activating glutaminolysis, thereby restrain detrimental caused inflammasome. Clinical sample analysis reveals adapts this metabolic environment through compensatory mutations anti-sigma-factor mucA, restore succinate-driven bioenergetics disrupt synchrony essential sustaining tolerance.
Language: Английский
Citations
0Cell Metabolism, Journal Year: 2025, Volume and Issue: unknown
Published: May 1, 2025
Language: Английский
Citations
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