The Cytotoxicity of Epsilon Toxin from Clostridium perfringens on Lymphocytes Is Mediated by MAL Protein Expression

被引:32
作者
Blanch, Marta [1 ,2 ,3 ]
Dorca-Arevalo, Jonatan [1 ,2 ,3 ]
Not, Anna [1 ]
Cases, Merce [1 ,2 ,3 ]
Gomez de Aranda, Inmaculada [1 ,3 ]
Martinez-Yelamos, Antonio [2 ,4 ]
Martinez-Yelamos, Sergio [2 ,4 ]
Solsona, Carles [1 ,2 ,3 ]
Blasi, Juan [1 ,2 ,3 ]
机构
[1] Univ Barcelona, Dept Pathol & Expt Therapeut, Lab Cellular & Mol Neurobiol, Campus Bellvitge, Barcelona, Spain
[2] Biomed Res Inst Bellvitge IDIBELL, Barcelona, Spain
[3] Univ Barcelona, Inst Neurosci, Barcelona, Spain
[4] Bellvitge Univ Hosp, Neurol Dept, Barcelona, Spain
关键词
Clostridium perfringens; multiple sclerosis; myelin and lymphocyte protein; T cell; epsilon toxin; pore-forming toxins; MDCK CELLS; TRANSPORT; GLUTAMATE; CLONING; BRAINS; ACTS;
D O I
10.1128/MCB.00086-18
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Epsilon toxin (Etx) from Clostridium perfringens 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 Clostridium perfringens on inflammatory and autoimmune diseases like multiple sclerosis.
引用
收藏
页数:18
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