Role of α-toxin-induced apoptosis of umbilical vein endothelial cells in vertical infection of Staphylococcus aureus L-form / 南方医科大学学报
Journal of Southern Medical University
; (12): 619-624, 2013.
Article
in En
| WPRIM
| ID: wpr-306498
Responsible library:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate α-toxin-induced apoptosis of umbilical vein endothelial cells and explore its role in vertical infection of Staphylococcus aureus L-form.</p><p><b>METHODS</b>HUV-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).</p><p><b>RESULTS</b>α-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.</p><p><b>CONCLUSION</b>α-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.</p>
Full text:
1
Database:
WPRIM
Main subject:
Staphylococcal Infections
/
Staphylococcus aureus
/
Bacterial Toxins
/
Cells, Cultured
/
Tumor Necrosis Factor-alpha
/
Apoptosis
/
Cell Biology
/
Toxicity
/
Caspase 3
/
Caspase 8
Limits:
Humans
Language:
En
Journal:
Journal of Southern Medical University
Year:
2013
Document type:
Article