Derrick Steven C, Morris Sheldon L
Laboratory of Mycobacterial Diseases and Cellular Immunology, Center for Biologics Evaluation and Research, United States Food and Drug Administration, Bethesda, MD 20892, USA.
Cell Microbiol. 2007 Jun;9(6):1547-55. doi: 10.1111/j.1462-5822.2007.00892.x. Epub 2007 Feb 9.
The secreted Mycobacterium tuberculosis protein, ESAT6, has been studied extensively in pathogenicity and vaccine experiments. Despite these studies little is known about the function of this protein. In this report, we demonstrate that ESAT6 induces apoptosis in THP-1 human macrophages using fluorescein isothiocyanate-Annexin V and intracellular caspase staining. We show that the induction of apoptosis by ESAT6 is dependent on the dose of the protein and the expression of caspase genes. Using real-time RT-PCR, we found that expression of caspase-1, -3, -5, -7 and -8 genes was upregulated in cells treated with ESAT6 relative to untreated cells. Furthermore, we show that while infection of THP-1 cells with wild-type M. tuberculosis strain H37Rv resulted in significant apoptosis 48 h post infection, a deletion mutant that does not express ESAT6 failed to induce significant apoptosis. Finally, experimental results using a cell impermeable fluorescent stain suggests that the formation of membrane pores may be a primary mechanism by which ESAT6 evokes an apoptotic response.
分泌型结核分枝杆菌蛋白ESAT6已在致病性和疫苗实验中得到广泛研究。尽管有这些研究,但对该蛋白的功能仍知之甚少。在本报告中,我们使用异硫氰酸荧光素 - 膜联蛋白V和细胞内半胱天冬酶染色证明ESAT6可诱导THP - 1人巨噬细胞凋亡。我们表明ESAT6诱导的凋亡取决于蛋白剂量和半胱天冬酶基因的表达。使用实时RT - PCR,我们发现与未处理细胞相比,用ESAT6处理的细胞中半胱天冬酶 - 1、-3、-5、-7和-8基因的表达上调。此外,我们表明,虽然用野生型结核分枝杆菌H37Rv菌株感染THP - 1细胞在感染后48小时导致显著凋亡,但不表达ESAT6的缺失突变体未能诱导显著凋亡。最后,使用细胞不可渗透荧光染料的实验结果表明,膜孔的形成可能是ESAT6引发凋亡反应的主要机制。