Roles of Reactive Oxygen Species in Rheumatoid Arthritis Pathogenesis.
10.4078/jrd.2016.23.6.340
- Author:
Su Jin YOO
1
;
Eunbyeol GO
;
Ye Eun KIM
;
Sunyoung LEE
;
Jaeyul KWON
Author Information
1. Department of Medical Education, Chungnam National University School of Medicine, Daejeon, Korea. kwonja@cnu.ac.kr
- Publication Type:Review
- Keywords:
Rheumatoid arthritis;
Reactive oxygen species;
NADPH oxidase;
Sirtuin 1;
Oxidative stress
- MeSH:
Arthritis, Rheumatoid*;
Autoantigens;
Autoimmune Diseases;
Cartilage;
DNA;
DNA Damage;
Immune System;
Mitochondria;
NADP;
NADPH Oxidase;
Oxidative Stress;
Oxidoreductases;
Reactive Oxygen Species*;
Receptors, Antigen, T-Cell;
Risk Factors;
Sirtuin 1;
Synovial Membrane;
Synovitis;
T-Lymphocytes
- From:Journal of Rheumatic Diseases
2016;23(6):340-347
- CountryRepublic of Korea
- Language:English
-
Abstract:
Rheumatoid arthritis (RA) is an autoimmune disease that starts with decreased tolerance to modified self-antigens and eventually leads to synovitis and destruction of bone and cartilage. Age is a risk factor for developing RA. Major changes in the immune system come with age due to chronic oxidative stress on the deoxyribonucleic acid (DNA) damage pathway, somatic mutation, modifications of auto-antigens, T cell tolerance and activation of fibroblast-like synoviocytes (FLS). Reactive oxygen species (ROS) generated by nicotinamide adenine dinucleotide phosphate oxidase 2 (NADPH oxidase 2) suppress T cell receptor signaling. Sirtuin 1 (SIRT1) is a critical immune suppressor of T cell activation and a key regulator of oxidative stress. When oxidative stress reduces activity of SIRT1, the breakdown of tolerance to modified self-antigens is expected. Generation of ROS can be perpetuated by enhanced DNA damage and dysfunctional mitochondria in a feedback loop during the development of RA. Through major T cell loss and selective proliferation of peripheral T cells, pro-inflammatory T cell pools with abnormal features are established in the T cell compartment. Hypoxic and inflammatory condition in synovium perpetuates ROS generation, which leads to the activation of FLS. In both T cell and synovium compartment, oxidative stress reshapes the immune system into the development of pre-clinical RA.
