1. Transient elevation of intracellular calcium ion levels as an early event in T-2 toxin-induced apoptosis in human promyelotic cell line HL-60
- Author
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Hiroki Okumura, Yoshio Ueno, Naoto Yoshino, Fumio Tashiro, Hidenori Akiba, Mitsuo Honda, and Mari Takizawa
- Subjects
Intracellular Fluid ,Microscopy, Confocal ,biology ,medicine.diagnostic_test ,Toxin ,Apoptosis ,HL-60 Cells ,Calpain ,Cell cycle ,Flow Cytometry ,Toxicology ,medicine.disease_cause ,Molecular biology ,Cell biology ,Flow cytometry ,T-2 Toxin ,Endonuclease ,Cell culture ,biology.protein ,medicine ,Humans ,Calcium ,Signal transduction - Abstract
Recently we have reported that T-2 toxin, a trichothecene mycotoxin produced by Fusarium species, is a potent inducer of apoptosis in the human promyelotic cell line HL-60. To clarify the signal transduction pathway of apoptosis primed by T-2 toxin, T-2 toxin-induced apoptosis was investigated in detail using confocal laser microscopy and flow cytometry. Apoptosis in HL-60 cells induced by T-2 toxin was dose dependent when the cells were treated with concentrations of 5-100 ng/ml for more than 2 hr. The apoptosis proceeds through various cell cycle stages of HL-60 cells. Prior to apoptosis, the intracellular calcium ion (Ca+2i) level was markedly elevated within 3-5 min after exposure to T-2 toxin and returned to normal level thereafter. A well-known chelator for Ca+2i, ethylene-N,N,N', N'-tetraacetic acid 4K acetoxymethyl ester (BAPTA-AM), a Ca+2-dependent endonuclease inhibitor ZnCl2, and calpain inhibitor 1 sharply blocked T-2 toxin-induced apoptosis. These results strongly suggest that the Ca+2 signal triggered by T-2 toxin is transduced by the activation of endonuclease and protease, and ultimately evokes apoptosis.
- Published
- 2006
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