» Articles » PMID: 38482018

Metabolic Changes in Fibroblast-like Synoviocytes in Rheumatoid Arthritis: State of the Art Review

Overview
Journal Front Immunol
Date 2024 Mar 14
PMID 38482018
Authors
Affiliations
Soon will be listed here.
Abstract

Fibroblast-like synoviocytes (FLS) are important components of the synovial membrane. They can contribute to joint damage through crosstalk with inflammatory cells and direct actions on tissue damage pathways in rheumatoid arthritis (RA). Recent evidence suggests that, compared with FLS in normal synovial tissue, FLS in RA synovial tissue exhibits significant differences in metabolism. Recent metabolomic studies have demonstrated that metabolic changes, including those in glucose, lipid, and amino acid metabolism, exist before synovitis onset. These changes may be a result of increased biosynthesis and energy requirements during the early phases of the disease. Activated T cells and some cytokines contribute to the conversion of FLS into cells with metabolic abnormalities and pro-inflammatory phenotypes. This conversion may be one of the potential mechanisms behind altered FLS metabolism. Targeting metabolism can inhibit FLS proliferation, providing relief to patients with RA. In this review, we aimed to summarize the evidence of metabolic changes in FLS in RA, analyze the mechanisms of these metabolic alterations, and assess their effect on RA phenotype. Finally, we aimed to summarize the advances and challenges faced in targeting FLS metabolism as a promising therapeutic strategy for RA in the future.

Citing Articles

Alpha-Taxilin: A Potential Diagnosis and Therapeutics Target in Rheumatoid Arthritis Which Interacts with Key Glycolytic Enzymes Associated with Metabolic Shifts in Fibroblast-Like Synoviocytes.

Sarkar A, Chakraborty D, Malik S, Mann S, Agnihotri P, Monu M J Inflamm Res. 2024; 17:10027-10045.

PMID: 39634288 PMC: 11615101. DOI: 10.2147/JIR.S465051.


Visnagin alleviates rheumatoid arthritis via its potential inhibitory impact on malate dehydrogenase enzyme: in silico, in vitro, and in vivo studies.

Khamis A, Sharshar A, Mohamed T, Abdelrasoul E, Salem M Genes Nutr. 2024; 19(1):20.

PMID: 39390383 PMC: 11465529. DOI: 10.1186/s12263-024-00756-3.

References
1.
Yu X, Li S . Non-metabolic functions of glycolytic enzymes in tumorigenesis. Oncogene. 2016; 36(19):2629-2636. DOI: 10.1038/onc.2016.410. View

2.
Liu Y, Rao P, Qian H, Shi Y, Chen S, Lan J . Regulatory Fibroblast-Like Synoviocytes Cell Membrane Coated Nanoparticles: A Novel Targeted Therapy for Rheumatoid Arthritis. Adv Sci (Weinh). 2022; 10(4):e2204998. PMC: 9896074. DOI: 10.1002/advs.202204998. View

3.
Xu K, Xu P, Yao J, Zhang Y, Hou W, Lu S . Reduced apoptosis correlates with enhanced autophagy in synovial tissues of rheumatoid arthritis. Inflamm Res. 2012; 62(2):229-37. DOI: 10.1007/s00011-012-0572-1. View

4.
Cushing L, Winkler A, Jelinsky S, Lee K, Korver W, Hawtin R . IRAK4 kinase activity controls Toll-like receptor-induced inflammation through the transcription factor IRF5 in primary human monocytes. J Biol Chem. 2017; 292(45):18689-18698. PMC: 5682975. DOI: 10.1074/jbc.M117.796912. View

5.
Kvacskay P, Yao N, Schnotz J, Scarpone R, Carvalho R, Klika K . Increase of aerobic glycolysis mediated by activated T helper cells drives synovial fibroblasts towards an inflammatory phenotype: new targets for therapy?. Arthritis Res Ther. 2021; 23(1):56. PMC: 7883459. DOI: 10.1186/s13075-021-02437-7. View