Protein phosphatase magnesium-dependent 1A induces inflammation in rheumatoid arthritisopen access
- Lee, Beomgu; Song, You Seon; Rhodes, Christopher; Goh, Tae Sik; Roh, Jong Seong; Jeong, Hoim; Park, Jisu; Lee, Han-Na; Lee, Seung-Geun; Kim, Soohyun; Kim, Mingyo; Lee, Sang-Il; Sohn, Dong Hyun; Robinson, William H.
- Issue Date
- ACADEMIC PRESS INC ELSEVIER SCIENCE
- PPM1A; Inflammation; DAMP; Rheumatoid arthritis
- BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.522, no.3, pp.731 - 735
- Journal Title
- BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Start Page
- End Page
- Rheumatoid arthritis (RA) is a highly inflammatory autoimmune disease. Although proinflammatory cytokines, including tumor necrosis factor (TNF) and interleukin (IL)-6, play a key role in the pathogenesis of RA, the causes of chronic inflammation are not fully understood. Here, we report that protein phosphatase magnesium-dependent 1A (PPM1A) levels were increased in RA synovial fluid compared with osteoarthritis (OA) synovial fluid and positively correlated with TNF levels. In addition, PPM1A expression was increased in synovial tissue from RA patients and joint tissue from a mouse model of arthritis. Finally, extracellular PPM1A induced inflammation by stimulating macrophages to produce TNF through toll-like receptor 4 (TLR4) and myeloid differentiation primary response protein 88 (MyD88) signaling pathway. Our findings suggest that extracellular PPM1A may contribute to the pathogenesis of RA by functioning as a damage-associated molecular pattern (DAMP) to induce inflammation. (C) 2019 Elsevier Inc. All rights reserved.
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- College of Medicine > Department of Medicine > Journal Articles
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