4.5 Article

Cytotoxic and apoptotic activities of the plancitoxin I from the venom of crown-of-thorns starfish (Acanthaster planci) on A375.S2 cells

期刊

JOURNAL OF APPLIED TOXICOLOGY
卷 35, 期 4, 页码 407-417

出版社

WILEY
DOI: 10.1002/jat.3034

关键词

crown-of-thorns starfish Acanthaster planci; venom; plancitoxin I; A375; S2; cytotoxicity; apoptosis

资金

  1. National Science Council, Taiwan
  2. Center of Excellence for Marine Bioenvironment and Biotechnology, National Taiwan Ocean University

向作者/读者索取更多资源

This study reports on a cytotoxic toxin derived from the venom of the crown-of-thorns starfish Acanthaster planci (CAV). The protein toxin was isolated through both ion-exchange and gel-filtration chromatography, and characterized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and mass spectrum analyzes. The CAV was identified as plancitoxin I protein. The mechanistic role of the CAV toxin was explored in human malignant melanoma A375.S2 cell death. The results indicated that after incubation with CAV toxin, cells significantly decreased in A375.S2 cell viability and increased in the lactate dehydrogenase (LDH) level in a dose-dependent manner. The assays indicated that CAV toxin promoted reactive oxygen species (ROS) production, induced nitric oxide (NO) formation, lost mitochondrial membrane potential (m) and induced inter-nucleosomal DNA fragmentation in A375.S2 cells. The molecular cytotoxicity of the CAV toxin was tested through evaluation of the apoptosis/necrosis ratio by double staining with annexin V-FITC and a propidium iodide (PI) assay. The results suggested that CAV toxin induced a cytotoxic effect in A375.S2 cells via the apoptotic procedure, and may be associated with the regulation of the p38 pathways. Copyright (c) 2014 John Wiley & Sons, Ltd. This study reports a cytotoxic toxin derived from the venom of the crown-of-thorns starfish Acanthaster planci (CAV). The CAV was identified as plancitoxin I protein. The results indicated that after incubation with CAV, cells significantly decreased in A375.S2 cell viability. The assays indicated that CAV toxin promoted ROS production, lost mitochondrial membrane potential and induced inter-nucleosomal DNA fragmentation in A375.S2 cells. The results suggested that CAV toxin induced a cytotoxic effect in A375.S2 cells via the apoptotic procedure.

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