Human adipose-derived mesenchymal stem cells attenuate collagen antibody-induced autoimmune arthritis by inducing expression of FCGIIB receptors

被引:5
|
作者
Yi, Hyoju [1 ]
Kang, Kwi Young [1 ,2 ]
Kim, Youngkyun [1 ]
Jung, Hyerin [1 ]
Rim, Yeri Alice [1 ]
Park, Narae [1 ]
Kim, Juryun [1 ]
Jung, Seung Min [1 ,2 ]
Park, Sung-Hwan [2 ]
Ju, Ji Hyeon [1 ,2 ]
机构
[1] Catholic Univ Korea, Seoul St Marys Hosp, Coll Med, CiSTEM Lab Convergent Res Consortium Immunol Dis, Seoul, South Korea
[2] Catholic Univ Korea, Seoul St Marys Hosp, Coll Med, Dept Internal Med,Div Rheumatol, Banpo Dong 137040, South Korea
基金
新加坡国家研究基金会;
关键词
Adipose-derived stem cell; Mesenchymal stem cell; Collagen antibody-induced arthritis; FC gamma receptors; T-CELLS; EMERGING ROLE; TISSUE; DIFFERENTIATION; INHIBIT; JOINT; INFLAMMATION; MACROPHAGES; ACTIVATION; INDUCTION;
D O I
10.1186/s12891-015-0634-y
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: Adipose-derived stem cells (ASCs) are mesenchymal stem cells (MSCs) derived from adipose tissue. MSCs have multiple properties including anti-inflammatory and immunomodulatory effects in various disease models and human diseases. However, the mechanisms underlying this wide range of effects need to be explored. Methods: Collagen antibody-induced arthritis (CAIA) is a unique model in which arthritis is rapidly and strongly induced. ASCs were intraperitoneally infused into CAIA mice before or after arthritis induction. The serum levels of various cytokines, adipokines, and chemokines were measured. The expression of FC gamma receptors (FCGRs) was investigated in peritoneal macrophages ex vivo. RAW264.7 cells and ASCs were co-cultured to elucidate the direct and indirect role of ASCs on FCGR expression. Results: ASCs attenuated arthritis in CAIA mice. Serum levels of tumor necrosis factor a, interleukin (IL)-15, resistin, and leptin were reduced in ASC-treated CAIA mice, whereas serum levels of IL-6 and adiponectin were not affected. In peritoneal macrophages isolated from ASC-treated mice, expression of FCGRIIB, which is immunoinhibitory, was higher than that of FCGRI. Co-culture of ASCs with RAW264.7 cells modulated the expression of FCGRs. The expression patterns and timings of peak expression differed among FCGRs. Expression of FCGRIIB was higher and peaked earlier than that of FCGRI. FCGRIII expression was not affected by this co-culture. Conclusions: This is a study to show that ASCs have anti-arthritic effects in CAIA mice. Modulation of FCGRs by ASCs might be a therapeutic mechanism in this antibody-associated arthritis model.
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页数:9
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