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Published on: July 16, 2021
Functional Regulation of Macrophage Phenotypes by MicroRNAs in Inflammatory Arthritis
Xiaoling Niu1,2, Grant S Schulert2
1Department of Nephrology and Rheumatology, Shanghai Children's Hospital, The Children's Hospital of Shanghai Jiaotong University, Pudong, China.
Abstract:
Inflammatory arthritis including rheumatoid arthritis (RA) and juvenile idiopathic arthritis (JIA) exhibit the shared feature of changes in activation and polarization of circulating monocytes and tissue macrophages. Numerous microRNAs (miRs) have been found to have key functions in regulating inflammation and macrophage polarization. Although there is increasing interest in the roles of miRs in both RA and JIA, less is known regarding how miRs relate to functional properties of immune cells, including monocytes and macrophages. Interestingly, miRs can function both to promote inflammatory phenotypes and pro-inflammatory polarization, as well as through negative-feedback loops to limit inflammation. Here, we review the functional roles of several miRs in macrophages in inflammatory arthritis, with a particular focus on vivo effects of miR alteration in experimental arthritis. We also consider how current efforts to target miRs clinically could modify functional monocyte and macrophage polarization in vivo, and serve as novel therapies for diseases such as RA and JIA.
Insights
MicroRNAs (miRs) influence immune cell function in inflammatory arthritis like rheumatoid arthritis (RA) and juvenile idiopathic arthritis (JIA). Targeting miRs may offer new therapeutic strategies for these conditions.
Area of Science:
- Immunology
- Molecular Biology
- Rheumatology
Background:
- Rheumatoid arthritis (RA) and juvenile idiopathic arthritis (JIA) involve altered monocyte and macrophage function.
- MicroRNAs (miRs) are key regulators of inflammation and macrophage polarization.
Purpose of the Study:
- To review the functional roles of miRs in macrophages within inflammatory arthritis.
- To examine the in vivo effects of miR alteration in experimental arthritis models.
- To consider the clinical potential of targeting miRs for monocyte and macrophage polarization in RA and JIA.
Main Methods:
- Literature review focusing on microRNA functions in macrophages.
- Analysis of experimental arthritis models with in vivo miR modulation.
- Evaluation of current miR-targeting strategies for clinical application.
Main Results:
- Specific miRs play critical roles in regulating macrophage polarization in inflammatory arthritis.
- In vivo studies demonstrate the impact of miR alteration on immune cell function.
- miRs can promote or limit inflammatory phenotypes through distinct mechanisms.
Conclusions:
- MicroRNAs are crucial modulators of immune cell behavior in inflammatory arthritis.
- Targeting miRs offers a promising avenue for novel therapeutic interventions in RA and JIA.
- Further research into in vivo miR effects is essential for clinical translation.
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