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Image Search Results
Journal: FEMS Immunology & Medical Microbiology
Article Title: Chlamydia (Chlamydophila) pneumoniae-induced cell death in human coronary artery endothelial cells is caspase-independent and accompanied by subcellular translocations of Bax and apoptosis-inducing factor
doi: 10.1111/j.1574-695x.2006.00083.x
Figure Lengend Snippet: Fig. 4. Subcellular translocation of Bax during Chlamydia pneumoniae infection of human coronary artery endothelial cells. (a) Cells were infected with Chamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-20 polyclonal antibody towards Bax and secondary antibody. Cells with a punctate fluorescence pattern were enumerated by fluorescence microscopy. Bars represent mean standard deviation of six or seven experiments. P o 0.05. (b) Subcellular localization of Bax in uninfected cells showing diffuse cytosolic fluores- cence. (c) Subcellular localization of Bax in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing punctate cytosolic fluorescence.
Article Snippet: Cells were washed twice in phosphate-buffered saline (PBS) and fixed in 4% paraformaldehyde in PBS for 15 min. After washing, cells were incubated for 30 min in
Techniques: Translocation Assay, Infection, Incubation, Microscopy, Standard Deviation
Journal: FEMS Immunology & Medical Microbiology
Article Title: Chlamydia (Chlamydophila) pneumoniae-induced cell death in human coronary artery endothelial cells is caspase-independent and accompanied by subcellular translocations of Bax and apoptosis-inducing factor
doi: 10.1111/j.1574-695x.2006.00083.x
Figure Lengend Snippet: Fig. 5. Subcellular translocation of apoptosis-inducing factor (AIF) dur- ing Chlamydia pneumoniae infection of human coronary artery endo- thelial cells. (a) Cells were infected with Chlamydia pneumoniae T45 at multiplicities of infection 1.25 or 10 for 8 h and incubated with N-19 polyclonal antibody towards AIF and secondary antibody. Cells with nuclear fluorescence were enumerated by fluorescence microscopy. Bars represent mean standard deviation of nine to 11 experiments. P o 0.05. (b) Subcellular localization of AIF in uninfected cells showing cytosolic fluorescence. (c) Subcellular localization of AIF in cells infected with C. pneumoniae, multiplicity of infection 1.25, for 24 h showing nuclear fluorescence.
Article Snippet: Cells were washed twice in phosphate-buffered saline (PBS) and fixed in 4% paraformaldehyde in PBS for 15 min. After washing, cells were incubated for 30 min in
Techniques: Translocation Assay, Infection, Incubation, Microscopy, Standard Deviation