Laboratory of Cellular and Molecular Neurobiology, Department of Pathology and Experimental Therapeutics, Campus of Bellvitge, University of Barcelona, Hospitalet de Llobregat, Barcelona, Spain.
Biomedical Research Institute of Bellvitge (IDIBELL), Hospitalet de Llobregat, Barcelona, Spain.
Mol Cell Biol. 2018 Sep 14;38(19). doi: 10.1128/MCB.00086-18. Print 2018 Oct 1.
Epsilon toxin (Etx) from is a pore-forming protein that crosses the blood-brain barrier, binds to myelin, and, hence, has been suggested to be a putative agent for the onset of multiple sclerosis, a demyelinating neuroinflammatory disease. Recently, myelin and lymphocyte (MAL) protein has been identified to be a key protein in the cytotoxic effect of Etx; however, the association of Etx with the immune system remains a central question. Here, we show that Etx selectively recognizes and kills only human cell lines expressing MAL protein through a direct Etx-MAL protein interaction. Experiments on lymphocytic cell lines revealed that MAL protein-expressing T cells, but not B cells, are sensitive to Etx and reveal that the toxin may be used as a molecular tool to distinguish subpopulations of lymphocytes. The overall results open the door to investigation of the role of Etx and on inflammatory and autoimmune diseases like multiple sclerosis.
来自 的 epsilon 毒素(Etx)是一种形成孔的蛋白质,可穿过血脑屏障,与髓鞘结合,因此被认为是多发性硬化症(一种脱髓鞘神经炎症性疾病)发病的潜在因素。最近,髓鞘和淋巴细胞(MAL)蛋白已被确定为 Etx 细胞毒性作用的关键蛋白;然而,Etx 与免疫系统的关联仍然是一个核心问题。在这里,我们通过直接的 Etx-MAL 蛋白相互作用表明,Etx 仅选择性地识别和杀死表达 MAL 蛋白的人类细胞系。对淋巴细胞系的实验表明,表达 MAL 蛋白的 T 细胞,而不是 B 细胞,对 Etx 敏感,这表明该毒素可用作区分淋巴细胞亚群的分子工具。总体结果为研究 Etx 和 在多发性硬化症等炎症和自身免疫性疾病中的作用开辟了道路。