کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2541110 1122641 2013 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Metformin downregulates Th17 cells differentiation and attenuates murine autoimmune arthritis
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی
پیش نمایش صفحه اول مقاله
Metformin downregulates Th17 cells differentiation and attenuates murine autoimmune arthritis
چکیده انگلیسی


• Metformin attenuated both arthritis scores and bone destruction in murine autoimmune arthritis.
• Metformin inhibited Th17 cell differentiation in vivo.
• Metformin treatment decreased the number of RORγt-expressing CD4 + cells in a dose-dependent manner.

IntroductionThis study was undertaken to determine whether metformin has anti-inflammatory effects in the collagen antibody-induced arthritis (CAIA) murine model. The effect of metformin on Th17 cell differentiation was also investigated.MethodsCAIA mice were treated with 100 and 150 mg/kg i.p. metformin (low- and high-dose groups, respectively). Arthritis activity and histological joint destruction were studied. Flow cytometry was used to (i) determine RORγt-expressing CD4 + percentages in draining axillary lymph nodes (ALNs) from metformin-treated and untreated mice with CAIA, (ii) determine Th17 percentages in splenic CD4 + T cells cultured ex vivo for 3 days in Th17-differentiation-inducing conditions, and (iii) determine the percentages of RORγt + CD4 + T cells when normal splenic T cells from DBA/1 mice were cultured in Th17-differentiation-inducing conditions together with various metformin doses. Western blot analysis was used to assess the intracellular signaling of the metformin-treated splenocytes.ResultsMetformin attenuated both arthritis scores and bone destruction in CAIA mice, decreased the serum levels of the pro-inflammatory cytokines, TNF-α and IL-1, and reduced the number of RORγt + CD4 + T cells in the ALNs. Splenocytes from metformin-treated CAIA mice differentiated less readily into Th17 cells upon ex vivo stimulation. Metformin treatment of normal cells cultured in Th17-differentiation-inducing conditions decreased the number of RORγt-expressing CD4 + cells in a dose-dependent manner and downregulated STAT3 phosphorylation via the AMPK pathway.ConclusionsMetformin had an anti-inflammatory effect on murine autoimmune arthritis due to the inhibition of Th17 cell differentiation. Metformin may have a possible therapeutic value for treatment of rheumatoid arthritis.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Immunopharmacology - Volume 16, Issue 1, May 2013, Pages 85–92
نویسندگان
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