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IL-10 induces TGF-β secretion, TGF-β receptor II upregulation, and IgA secretion in B cells
European Cytokine Network ( IF 2.2 ) Pub Date : 2020-02-06 , DOI: 10.1684/ecn.2019.0434
Yasser Bagheri 1, 2 , Fateme Babaha 1 , Reza Falak 2 , Reza Yazdani 3 , Gholamreza Azizi 4 , Maryam Sadri 5 , Hassan Abolhassani 6 , Mehdi Shekarabi 2 , Asghar Aghamohammadi 3
Affiliation  

Background: Interleukin-10 (IL-10) is a pleiotropic cytokine, which has both regulatory and stimulatory effects on different immune cell types. Different studies have reported the importance of IL-10 and Transforming growth factor-beta (TGF-p) in the regulation of B cell class switching the production of immunoglobulin A (IgA); however, the underlying mechanisms remain to be fully elucidated. The objective of this study was to investigate the TGF-p response during B stimulation of human B cells by IL-10. Methods: Pan B cells of healthy donors were negatively purified by a magnetic cell separation technique. B cells were cultured with multimeric CD40 ligand (mCD40L) and IL-10 for two and seven days. After harvesting in specific days, TGF-p receptor II and surface IgA expression was determined by flow cytometry, while IgA and TGF-p secretion was assessed by enzyme-linked immunosorbent assay. Results: B cells endogenously expressed TGF-p receptor II and after 48 hours cultivation with mCD40L or mCD40L plus IL-10, both the expression of this receptor and the production of TGF-p were significantly increased. Notably, TGF-p levels following stimulation with mCD40L and IL-10 were higher than those produced by B cells stimulated with mCD40L alone. Furthermore, at day 7 and following IL-10 stimulation, there was a significant rise in the amount of IgA secretion by class-switched plasma cells, which was higher than stimulation with mCD40L alone. Conclusion: Our findings suggest that IL-10 can modulate TGF-p production and TGF-p receptor expression in mCD40-activated human B lymphocytes.



中文翻译:

IL-10 诱导 B 细胞中 TGF-β 分泌、TGF-β 受体 II 上调和 IgA 分泌

背景:白介素10(IL-10)是一种多效细胞因子,对不同类型的免疫细胞具有调节和刺激作用。不同的研究报道了 IL-10 和转化生长因子-β (TGF-p) 在调节 B 细胞类别转换免疫球蛋白 A (IgA) 产生中的重要性;然而,其根本机制仍有待充分阐明。本研究的目的是研究 IL-10 刺激人类 B 细胞期间 TGF-β 的反应。方法:通过磁性细胞分离技术对健康供体的 Pan B 细胞进行负纯化。 B 细胞与多聚 CD40 配体 (mCD40L) 和 IL-10 一起培养 2 天和 7 天。在特定天数收获后,通过流式细胞术测定TGF-β受体II和表面IgA表达,同时通过酶联免疫吸附测定评估IgA和TGF-β分泌。结果:B细胞内源表达TGF-β受体II,与mCD40L或mCD40L加IL-10培养48小时后,该受体的表达和TGF-β的产生均显着增加。值得注意的是,用 mCD40L 和 IL-10 刺激后的 TGF-β 水平高于仅用 mCD40L 刺激的 B 细胞产生的水平。此外,在第7天和IL-10刺激后,类别转换浆细胞的IgA分泌量显着增加,高于单独使用mCD40L的刺激。结论:我们的研究结果表明,IL-10 可以调节 mCD40 激活的人 B 淋巴细胞中 TGF-β 的产生和 TGF-β 受体的表达。

更新日期:2020-02-06
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