Mycobacterium tuberculosis antigen Wag31 induces expression of C-chemokine XCL2 in macrophages

被引:15
作者
Cao, Wei [2 ]
Tang, Shuai [2 ]
Yuan, Hanying [2 ]
Wang, Honghai [2 ]
Zhao, Xin [1 ]
Lu, Hong [2 ]
机构
[1] McGill Univ, Dept Anim Sci, Quebec City, PQ, Canada
[2] Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
基金
加拿大自然科学与工程研究理事会; 中国国家自然科学基金;
关键词
D O I
10.1007/s00284-008-9172-2
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学]; 100705 [微生物与生化药学];
摘要
Tuberculosis is still a major threat to human health. To date, only approximately half of the proteins encoded by Mycobacterium tuberculosis H37Rv have been assigned specific functions. Wag31 (Rv2145c) is one of the bacterial proteins whose function is mostly unknown. Using a modified split-ubiquitin membrane yeast two-hybrid system, we screened a macrophage cDNA library with Wag31 as bait and identified XCL2, a C-subfamily chemokine, as a binding partner for Wag31. More importantly, Wag31 was found to specifically stimulate XCL2 expression in macrophages. The results from this study demonstrate that expression of C-chemokine is not restricted to certain types of T cells and natural killer cells. Because C-chemokine is chemotactic for CD8+ and CD4+ T cells, our novel findings could provide a new mechanism by which the bacteria induce cell-mediated immunity and by which Wag31 could be a potential target for controlling M. tuberculosis infection.
引用
收藏
页码:189 / 194
页数:6
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