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Cited 8 time in webofscience Cited 8 time in scopus
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Protein phosphatase magnesium-dependent 1A induces inflammation in rheumatoid arthritisopen access

Authors
Lee, BeomguSong, You SeonRhodes, ChristopherGoh, Tae SikRoh, Jong SeongJeong, HoimPark, JisuLee, Han-NaLee, Seung-GeunKim, SoohyunKim, MingyoLee, Sang-IlSohn, Dong HyunRobinson, William H.
Issue Date
12-Feb-2020
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
PPM1A; Inflammation; DAMP; Rheumatoid arthritis
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.522, no.3, pp.731 - 735
Indexed
SCIE
SCOPUS
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
522
Number
3
Start Page
731
End Page
735
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/6923
DOI
10.1016/j.bbrc.2019.11.112
ISSN
0006-291X
Abstract
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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의과대학 (의학과)
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