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豚鼠中分枝杆菌索状因子受体的特性研究

Characterization of the receptors for mycobacterial cord factor in Guinea pig.

作者信息

Toyonaga Kenji, Miyake Yasunobu, Yamasaki Sho

机构信息

Division of Molecular Immunology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.

Division of Molecular Immunology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan ; Research Center for Advanced Immunology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.

出版信息

PLoS One. 2014 Feb 12;9(2):e88747. doi: 10.1371/journal.pone.0088747. eCollection 2014.

Abstract

Guinea pig is a widely used animal for research and development of tuberculosis vaccines, since its pathological disease process is similar to that present in humans. We have previously reported that two C-type lectin receptors, Mincle (macrophage inducible C-type lectin, also called Clec4e) and MCL (macrophage C-type lectin, also called Clec4d), recognize the mycobacterial cord factor, trehalose-6,6'-dimycolate (TDM). Here, we characterized the function of the guinea pig homologue of Mincle (gpMincle) and MCL (gpMCL). gpMincle directly bound to TDM and transduced an activating signal through ITAM-bearing adaptor molecule, FcRγ. Whereas, gpMCL lacked C-terminus and failed to bind to TDM. mRNA expression of gpMincle was detected in the spleen, lymph nodes and peritoneal macrophages and it was strongly up-regulated upon stimulation of zymosan and TDM. The surface expression of gpMincle was detected on activated macrophages by a newly established monoclonal antibody that also possesses a blocking activity. This antibody potently suppressed TNF production in BCG-infected macrophages. Collectively, gpMincle is the TDM receptor in the guinea pig and TDM-Mincle axis is involved in host immune responses against mycobacteria.

摘要

豚鼠是一种广泛用于结核病疫苗研发的动物,因为其病理疾病过程与人类相似。我们之前报道过,两种C型凝集素受体,Mincle(巨噬细胞诱导性C型凝集素,也称为Clec4e)和MCL(巨噬细胞C型凝集素,也称为Clec4d),可识别分枝杆菌索状因子,海藻糖-6,6'-二霉菌酸酯(TDM)。在此,我们对豚鼠Mincle(gpMincle)和MCL(gpMCL)同源物的功能进行了表征。gpMincle直接与TDM结合,并通过含免疫受体酪氨酸激活基序(ITAM)的衔接分子FcRγ转导激活信号。然而,gpMCL缺乏C末端,无法与TDM结合。在脾脏、淋巴结和腹腔巨噬细胞中检测到gpMincle的mRNA表达,在酵母聚糖和TDM刺激后其表达强烈上调。通过一种新建立的、也具有阻断活性的单克隆抗体,在活化巨噬细胞上检测到了gpMincle的表面表达。该抗体有效抑制了卡介苗感染的巨噬细胞中TNF的产生。总的来说,gpMincle是豚鼠中的TDM受体,TDM-Mincle轴参与宿主针对分枝杆菌的免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdc8/3923057/8b96929fd569/pone.0088747.g001.jpg

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