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滤泡树突状细胞分泌蛋白 FDC-SP 控制 IgA 的产生。

Follicular dendritic cell secreted protein FDC-SP controls IgA production.

机构信息

Department of Immunology, University of Manitoba, Winnipeg, Manitoba, Canada.

Department of Pathology, University of Manitoba, Winnipeg, Manitoba, Canada.

出版信息

Mucosal Immunol. 2014 Jul;7(4):948-57. doi: 10.1038/mi.2013.113. Epub 2014 Jan 8.

DOI:10.1038/mi.2013.113
PMID:24399151
Abstract

Follicular dendritic cell secreted protein (FDC-SP) is a secreted peptide predominantly expressed in mucosal tissues. We previously reported that FDC-SP transgenic mice have altered B-cell responses to systemic immunization; however, the role of FDC-SP in mucosal immunity is unknown. Here, we report that FDC-SP functions in regulating immunoglobulin A production. FDC-SP transgenic mice show decreased IgA levels in serum, saliva, and bronchoalveolar lavage fluid. Reciprocally, FDC-SP-deficient mice show significantly increased IgA levels in serum and intestinal lavage, associated with accumulation of IgA+ cells in blood, bone marrow, Peyer's patches, and lymph nodes. FDC-SP-deficient mice generated higher titers of antigen-specific IgA but normal IgG1 responses upon immunization. Purified FDC-SP transgenic B cells generated decreased IgA responses to transforming growth factor β (TGFβ)+interleukin 5 (IL5) stimulation. Consistent with a direct effect of FDC-SP on B cells, recombinant FDC-SP suppressed B-cell IgA production in vitro. Six- to 14-month-old FDC-SP-deficient mice show IgA deposition in kidney glomeruli, which was associated with proteinuria and pathology consistent with mild IgA nephropathy (IgAN). Our results demonstrate a novel biological activity of FDC-SP in controlling B-cell IgA production and identify FDC-SP-deficient mice as a novel mouse model of IgAN.

摘要

滤泡树突状细胞分泌蛋白(FDC-SP)是一种主要在黏膜组织中表达的分泌肽。我们之前报道过,FDC-SP 转基因小鼠对系统性免疫的 B 细胞反应发生改变;然而,FDC-SP 在黏膜免疫中的作用尚不清楚。在这里,我们报告 FDC-SP 可调节免疫球蛋白 A 的产生。FDC-SP 转基因小鼠的血清、唾液和支气管肺泡灌洗液中的 IgA 水平降低。相反,FDC-SP 缺陷型小鼠的血清和肠道灌洗液中的 IgA 水平显著升高,伴有血液、骨髓、派尔集合淋巴结和淋巴结中 IgA+细胞的积累。FDC-SP 缺陷型小鼠在免疫接种时产生更高滴度的抗原特异性 IgA,但 IgG1 反应正常。经转化生长因子 β(TGFβ)+白细胞介素 5(IL5)刺激,纯化的 FDC-SP 转基因 B 细胞产生的 IgA 反应降低。与 FDC-SP 对 B 细胞的直接作用一致,重组 FDC-SP 在体外抑制 B 细胞 IgA 产生。6-14 月龄的 FDC-SP 缺陷型小鼠的肾脏肾小球中有 IgA 沉积,与蛋白尿和符合轻度 IgA 肾病(IgAN)的病理学有关。我们的结果表明 FDC-SP 在控制 B 细胞 IgA 产生方面具有新的生物学活性,并确定 FDC-SP 缺陷型小鼠为 IgAN 的新型小鼠模型。

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