Role of α-toxin-induced apoptosis of umbilical vein endothelial cells in vertical infection of Staphylococcus aureus L-form.
- Author:
Junchang GUAN
1
;
Xiang ZHU
;
Fengling YU
;
Wenxuan YANG
;
Tingting LIU
;
Tao ZHANG
;
Na LIN
;
Yong LIU
;
Congsen LIU
Author Information
- Publication Type:Journal Article
- MeSH: Apoptosis; Bacterial Toxins; toxicity; Caspase 3; metabolism; Caspase 8; metabolism; Cells, Cultured; Human Umbilical Vein Endothelial Cells; cytology; Humans; L Forms; Staphylococcal Infections; Staphylococcus aureus; Tumor Necrosis Factor-alpha; metabolism
- From: Journal of Southern Medical University 2013;33(5):619-624
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo investigate α-toxin-induced apoptosis of umbilical vein endothelial cells and explore its role in vertical infection of Staphylococcus aureus L-form.
METHODSHUV-EC-C cells exposed to different concentrations (0, 10, 30, 90, and 270 ng/ml) of α-toxin for different time lengths (0, 2, 4, 6, and 8 h) were examined for apoptosis using flow cytometry with Annexin V-PI staining. The levels of tumor necrosis factor-α (TNF-α) and the activities of, caspase-3 and caspase-8 in the cell culture were detected by ELISA and colorimetric method, respectively. α-Toxin-induced cell apoptosis was also analyzed in HUV-EC-C cells treated with a neutralizing antibody of TNF-α or with the inhibitory peptides of caspase-3 (zDEVD-FMK) and caspase-8 (zIETD-fmk).
RESULTSα-Toxin induced apoptosis of HUV-EC-C cells in a dose- and time-dependent manner and caused significantly enhanced expression of TNF-α and the activation of both caspase-3 and caspase-8. Inhibition of TNF-α with its neutralizing antibody and the inhibitory peptides of caspase-3 or -8 all significantly decreased α-toxin-induced cell apoptosis, and the caspase-3 inhibitor completely blocked α-toxin-induced cell apoptosis.
CONCLUSIONα-Toxin-induced apoptosis is partially mediated by the extrinsic cell death pathway of TNF-α and caspase-8 and plays an important role in the vertical infection of S. aureus L-form to affect fetal growth and development.