| Literature DB >> 27021182 |
Liang Wu1,2, Xiao Wang2, Yunhui Li2, Yuan Liu2, Danhua Su2, Tao Fu2, Fei Guo2, Liangping Gu2, Xugan Jiang2, Shengxia Chen3, Jianping Cao4.
Abstract
Toxoplasma gondii is an obligate intracellular parasite that may manipulate host cell mitochondrial apoptosis pathways. In our experiment, 293T cells were transfected with the p3×FLAG-CMV-Myc-ROP18 vector and expressed the ROP18-Myc fusion protein. Cell apoptosis was induced by 0.5 μg/mL actinomycin D (ActD) and was detected by Annexin V-FITC/PI assay. The cell mitochondrial membrane potential was determined by JC-1. Cytochrome c (Cyto-c) from mitochondria and the cytoplasm was measured by Western blot. The Bcl-2 and Bax coding gene expression levels were detected by real-time PCR. We found, in vitro, that T. gondii ROP18 significantly suppressed 293T cell apoptosis induced by ActD and maintained mitochondrial membrane potential and integrity, thereby preventing the release of Cyto-c from mitochondria into the cytoplasm. The ratio of Bcl-2/Bax in ROP18-overexpressing cells was significantly higher than that of the negative control. Therefore, we speculate that ROP18 could suppress host cell apoptosis via the mitochondrial apoptosis pathway in vitro.Entities:
Keywords: Apoptosis; Mitochondrial apoptosis pathway; ROP18; Toxoplasma gondii
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Year: 2016 PMID: 27021182 DOI: 10.1007/s00436-016-4993-6
Source DB: PubMed Journal: Parasitol Res ISSN: 0932-0113 Impact factor: 2.289