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

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

  • Sci Rep. 2021 Aug 27;11(1):17312. doi: 10.1038/s41598-021-96530-1.
Hirotaka Yamada 1 Jun Saegusa 2 3 Sho Sendo 1 Yo Ueda 1 Takaichi Okano 1 4 Masakazu Shinohara 5 6 Akio Morinobu 1
Affiliations

Affiliations

  • 1 Department of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan.
  • 2 Department of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Kobe, Japan. [email protected].
  • 3 Department of Clinical Laboratory, Kobe University Hospital, Kobe, Japan. [email protected].
  • 4 Department of Clinical Laboratory, Kobe University Hospital, Kobe, Japan.
  • 5 Division of Epidemiology, Kobe University Graduate School of Medicine, Kobe, Japan.
  • 6 The Integrated Center for Mass Spectrometry, Kobe University Graduate School of Medicine, Kobe, Japan.
Abstract

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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