Song Jiangping, Chen Xiao, Wang Mangyuan, Xing Yong, Zheng Zhe, Hu Shengshou
State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, 167A Beilishi Road, Xi Cheng District, Beijing. 100037, China.
Sci Rep. 2014 Dec 23;4:7583. doi: 10.1038/srep07583.
The mechanism of immune tolerance is to be further understood. The present study aims to investigate the role of the Cardiac endothelial cell (CEC)-derived exosomes in the induction of regulatory B cells. In this study, CECs were isolated from the mouse heart. Exosomes were purified from the culture supernatant of the primary endothelial cells. The suppressor functions of the regulatory B cells were determined by flow cytometry. The results showed that the CEC-derived exosomes carried integrin αvβ6. Exposure to lipopolysaccharide (LPS) induced B cells to express the latent transforming growth factor (TGF)-β, the latter was converted to the active form, TGF-β, by the exosome-derived αvβ6. The B cells released TGF-β in response to re-exposure to the exosomes in the culture, which suppressed the effector T cell proliferation. We conclude that CEC-derived exosomes have the capacity to induce B cells with immune suppressor functions.
免疫耐受的机制有待进一步了解。本研究旨在探讨心脏内皮细胞(CEC)衍生的外泌体在诱导调节性B细胞中的作用。在本研究中,从小鼠心脏中分离出CEC。从原代内皮细胞的培养上清液中纯化出外泌体。通过流式细胞术确定调节性B细胞的抑制功能。结果表明,CEC衍生的外泌体携带整合素αvβ6。暴露于脂多糖(LPS)可诱导B细胞表达潜伏转化生长因子(TGF)-β,后者被外泌体衍生的αvβ6转化为活性形式的TGF-β。B细胞在培养中再次暴露于外泌体时会释放TGF-β,从而抑制效应T细胞增殖。我们得出结论,CEC衍生的外泌体具有诱导具有免疫抑制功能的B细胞的能力。