Journal of Molecular Medicine, Journal Year: 2025, Volume and Issue: unknown
Published: May 21, 2025
Language: Английский
Journal of Molecular Medicine, Journal Year: 2025, Volume and Issue: unknown
Published: May 21, 2025
Language: Английский
Cytokine, Journal Year: 2025, Volume and Issue: 186, P. 156852 - 156852
Published: Jan. 6, 2025
Language: Английский
Citations
1Cellular and Molecular Immunology, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 26, 2025
Abstract Macrophage polarization and energy metabolic reprogramming play pivotal roles in the onset progression of inflammatory arthritis. Moreover, although previous studies have reported that proviral integration Moloney virus 2 (Pim2) kinase is involved various cancers through mediation aerobic glycolysis cancer cells, its role arthritis remains unclear. In this study, we demonstrated multiple enzymes are activated upon Pim2 upregulation during M1 macrophage polarization. Specifically, directly phosphorylates PGK1-S203, PDHA1-S300, PFKFB2-S466, thereby promoting glycolytic reprogramming. expression was elevated macrophages from patients with collagen-induced (CIA) model mice. Conditional knockout or administration inhibitor HJ-PI01 attenuated development by inhibiting Through molecular docking dynamic simulation, bexarotene identified as an inhibits downstream polarization, mitigating For targeted treatment, neutrophil membrane-coated (Bex)-loaded PLGA-based nanoparticles (NM@NP-Bex) were developed to slow suppressing macrophages, these (NPs) exhibited superior therapeutic effects fewer side effects. Taken together, results our study targeting inhibition could effectively alleviate via reversal M1/M2 imbalance. NM@NPs loaded represent a promising strategy for treatment
Language: Английский
Citations
1Biology, Journal Year: 2025, Volume and Issue: 14(4), P. 428 - 428
Published: April 16, 2025
Chronic inflammatory diseases, such as rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), multiple sclerosis (MS), atherosclerosis, and bowel disease (IBD), pose major global health concerns. These disorders are marked by persistent inflammation, immune system dysfunction, tissue injury, fibrosis, ultimately leading to severe organ dysfunction diminished quality of life. Osteopontin (OPN), a multifunctional extracellular matrix protein, plays crucial role in regulation, remodeling. It promotes cell recruitment, stimulates pro-inflammatory cytokine production, contributes fibrosis through interactions with integrins CD44 receptors. Additionally, OPN activates key pathways, including NF-κB, MAPK, PI3K/Akt, further aggravating damage chronic conditions. Our review highlights the its potential biomarker, therapeutic implications. We explore promising preclinical approaches, monoclonal antibodies, small molecule inhibitors, natural compounds like curcumin, which have demonstrated mitigating OPN-driven inflammation. However, challenges persist selectively targeting while maintaining essential physiological roles, bone remodeling wound healing. offers insights into strategies future research directions.
Language: Английский
Citations
1Nanoscale, Journal Year: 2024, Volume and Issue: 16(32), P. 14975 - 14993
Published: Jan. 1, 2024
Rheumatoid arthritis (RA) is a progressive autoimmune disease that mainly affects the inner lining of synovial joints and leads to chronic inflammation. While RA not known as lethal, recent research indicates it may be silent killer because its strong association with an increased risk lung heart diseases. Patients develop these systemic consequences due regular uptake heavy drugs such disease-modifying antirheumatic medications (DMARDs), glucocorticoids (GCs), nonsteroidal anti-inflammatory medicines (NSAIDs),
Language: Английский
Citations
6The Lancet Rheumatology, Journal Year: 2025, Volume and Issue: unknown
Published: March 1, 2025
Language: Английский
Citations
0medRxiv (Cold Spring Harbor Laboratory), Journal Year: 2025, Volume and Issue: unknown
Published: April 4, 2025
Abstract Background Inflammatory processes and metabolic activity significantly influence the beginning course of systemic sclerosis (SSc). This study aims to explore genetic basis for impact inflammation metabolism on susceptibility SSc. Methods We used three types exposure: 91 inflammatory proteins (14,824 participants), 731 immune cell traits (3,757 Sardinians), 1,400 blood metabolites (8,299 Europeans), with SSc as an outcome (680 cases, 399,355 controls). A two-sample multivariate bivariate Mendelian randomization (MR) was conducted investigate causal relationship between inflammation, metabolism, interaction proteins, cells, in Results MR analysis identified potential associations four fourteen a significant association two cells Among them, HLA DR CD14- CD16+ monocyte CD33dim DR+ CD11b+ reduced risk Pleiotropy heterogeneity were not observed. None showed bidirectional causality reverse analysis. Multivariate results independent effects one cell, SSc; factors (hepatocyte growth factor, stem 5-hydroxyindole sulfate levels); protective (HLA monocyte, Homoarginine levels Tetradecadienoate (14:2) levels). Conclusions These findings reveal relationships interactions fifteen traits, its development, offering fresh perspectives mechanisms underlying guiding choice treatment approaches.
Language: Английский
Citations
0BMC Rheumatology, Journal Year: 2025, Volume and Issue: 9(1)
Published: April 22, 2025
Language: Английский
Citations
0Journal of Autoimmunity, Journal Year: 2025, Volume and Issue: 154, P. 103424 - 103424
Published: April 28, 2025
Language: Английский
Citations
0Biochemical Pharmacology, Journal Year: 2025, Volume and Issue: 238, P. 116973 - 116973
Published: May 6, 2025
Language: Английский
Citations
0Journal of Molecular Medicine, Journal Year: 2025, Volume and Issue: unknown
Published: May 21, 2025
Language: Английский
Citations
0