Effect of resolvin D5 on T cell differentiation and osteoclastogenesis analyzed by lipid mediator profiling in the experimental arthritis

被引:18
|
作者
Yamada, Hirotaka [1 ]
Saegusa, Jun [1 ,2 ]
Sendo, Sho [1 ]
Ueda, Yo [1 ]
Okano, Takaichi [1 ,2 ]
Shinohara, Masakazu [3 ,4 ]
Morinobu, Akio [1 ]
机构
[1] Kobe Univ, Dept Rheumatol & Clin Immunol, Grad Sch Med, Kobe, Hyogo, Japan
[2] Kobe Univ Hosp, Dept Clin Lab, Kobe, Hyogo, Japan
[3] Kobe Univ, Div Epidemiol, Grad Sch Med, Kobe, Hyogo, Japan
[4] Kobe Univ, Integrated Ctr Mass Spectrometry, Grad Sch Med, Kobe, Hyogo, Japan
关键词
DOCOSAHEXAENOIC ACID; RHEUMATOID-ARTHRITIS; RESOLUTION; MECHANISMS; INFLAMMATION; DISEASE; E1;
D O I
10.1038/s41598-021-96530-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Resolvins, are specialized pro-resolving mediators (SPMs) derived from n-3 polyunsaturated fatty acids. They contribute actively to the resolution of inflammation, but little is known concerning their role in chronic inflammation, such as in rheumatoid arthritis (RA). Here, we performed lipid mediator (LM) profiling in tissues from the paws of SKG arthritic mice using lipid chromatography (LC)/mass spectrometry (MS)/MS-based LM metabololipidomics. We found elevated levels of SPMs including resolvin D5 (RvD5) in these tissues. Moreover, RvD5 levels were significantly correlated with arthritis disease activity. From experiments to assess the role of RvD5 in the pathology of RA, we concluded that RvD5 suppressed Th17 cell differentiation and facilitated regulatory T cell differentiation, as well as inhibiting CD4(+) T cell proliferation. Furthermore, RvD5 attenuated osteoclast differentiation and interfered with osteoclastogenesis. Targeting the resolution of inflammation could be promising as a novel treatment for RA.
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页数:11
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