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食管癌来源的微泡可诱导调节性B细胞。

Esophageal cancer-derived microvesicles induce regulatory B cells.

作者信息

Li Yun, An Jun, Huang Shaohong, He Jinyuan, Zhang Junhang

机构信息

Department of Cardiothoracic Surgery, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.

出版信息

Cell Biochem Funct. 2015 Jul;33(5):308-13. doi: 10.1002/cbf.3115. Epub 2015 May 25.

Abstract

The role of B cells in the generation of cancer-immune tolerance is unclear. This study aims to investigate the role of cancer-derived microvesicles (Mvcs) in the generation of transforming growth factor (TGF)-β(+) B cells. In this study, esophageal cancer (Eca) cells were isolated from surgically removed cancer tissue. Mvcs were purified from the culture supernatant and characterized by Western blotting. The immune suppression assay was carried out with a cell culture model and flow cytometry. The results showed that Eca-derived Mvcs were LAMP1 positive and carried MMP9. Exposure to the Mvcs induces naive B cells to differentiate into TGF-β-producing regulatory B cells; the latter show immune suppressor functions on CD8(+) T-cell proliferation. In conclusion, Eca-derived Mvc can induce TGF-β(+) B cells; the latter suppress CD8(+) T-cell activities. The MMP9-laden Mvcs may be a new therapeutic target in the treatment of Eca.

摘要

B细胞在癌症免疫耐受产生中的作用尚不清楚。本研究旨在探讨癌症来源的微泡(Mvcs)在转化生长因子(TGF)-β(+)B细胞产生中的作用。在本研究中,从手术切除的癌组织中分离出食管癌细胞(Eca)。从培养上清液中纯化Mvcs,并通过蛋白质印迹法进行表征。采用细胞培养模型和流式细胞术进行免疫抑制测定。结果表明,Eca来源的Mvcs为LAMP1阳性并携带MMP9。暴露于Mvcs可诱导幼稚B细胞分化为产生TGF-β的调节性B细胞;后者对CD8(+)T细胞增殖具有免疫抑制功能。总之,Eca来源的Mvc可诱导TGF-β(+)B细胞;后者抑制CD8(+)T细胞活性。携带MMP9的Mvcs可能是治疗Eca的新治疗靶点。

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