The regulatory role of Mcl-1 in apoptosis of mouse peritoneal macrophage infected with M. tuberculosis strains that differ in virulence

Purpose: Myeloid cell leukaemia-1 (Mcl-1) is a valuable target in tumour treatments. However, several reports have suggested that Mcl-1 may play a role in tuberculosis infection. Therefore, we investigated the function of Mcl-1 in tuberculosis infection and the underlying regulatory mechanism. Methods: Mcl-1-shRNA was used to down-regulate Mcl-1 expression in BCG-, H37Ra-, H37Rvand XJ-MTB-infected mouse peritoneal macrophages. TUNEL staining detected macrophage apoptosis. The colony-forming units (CFUs) were determined to assess the Mycobacterium tuberculosis (MTB) clearance after down-regulating Mcl-1. Immunohistochemical analysis of Mcl-1 expression in mouse peritoneal macrophages was performed. Haematoxylin and eosin staining detected pathologic damage of the liver, spleen, lung, and kidney in mice. Real-time PCR and Western blotting determined the expression of cytochrome-c in Mcl-1-shRNA-treated mouse peritoneal macrophages infected with MTB strains that differ in virulence. Results: Mcl-1-shRNA significantly promoted host macrophage apoptosis and cytochrome-c induction, and the apoptotic induction of the XJ-MTB and H37Rv strains was stronger than the H37Ra and BCG strains (P<0.05). Apoptotic protein cytochrome-c levels continued to increase in mouse peritoneal macrophages infected MTB before and after treatment, Caspase-8 levels only slightly increased after Mcl-1-shRNA-treated (P<0.05), but the increase of Cytochrome-c have no significant differences compared with Caspase-8 levels (P>0.05). Conclusion: Mcl-1-shRNA intervention effectively down-regulated Mcl-1 expression, significantly increased host macrophage apoptosis, and induced cytochrome-c expression in mouse peritoneal macrophages infected with MTB strains of different virulence, and these changes were influenced by the virulence of the MTB strains. The mitochondriamediated intrinsic apoptotic pathway play an important role before Mcl-1-shRNA-trated, and then with the extrinsic apoptotic pathway co-regulate host macrophage apoptosis.