期刊论文详细信息
FEBS Letters
Maitotoxin, a potent, general activator of phosphoinositide breakdown
Gusovsky, Fabian1  Daly, John W.1  Yasumoto, Takeshi2 
[1] Laboratory of Bioorganic Chemistry, NIDDK, National Institutes of Health, Bethesda, MD 20892, USA;Faculty of Agriculture, Tohoku University, Sendai, Japan
关键词: Maitotoxin;    Phosphoinositide breakdown;    Ca2+ channel;   
DOI  :  10.1016/0014-5793(89)80151-6
学科分类:生物化学/生物物理
来源: John Wiley & Sons Ltd.
PDF
【 摘 要 】

Maitotoxin (MTX), a potent marine toxin, elicits a calcium-dependent activation of cells that can be inhibited by calcium channel blockers like nifedipine. MTX also stimulates phosphoinositide breakdown in smooth muscle cells, NCB-20 cells and PC12 cells through a nifedipine-insensitive mechanism. We now report that MTX stimulates phosphoinositide breakdown in a wide variety of cells, and appears to repesent the first general activator of this second messenger-generating system. MTX-induced stimulation of phosphoinositide breakdown is dependent in every cell line on the presence of extracellular calcium. In differentiated HL60 cells, in which a chemotactic peptide (fMLP) activates phosphoinositide breakdown via a pertussis toxin-sensitive mechanism, MTX-induced stimulation is not affected by pertussis toxin treatment. A phorbol ester has no effect on the response to MTX. Thus, MTX stimulates phosphoinositide breakdown through a calcium-dependent mechanism that at least in three cell lines (PC12, NCB20 and HL60) is not mediated by a pathway that involves a pertussis toxin-sensitive guanine nucleotide-binding protein.

【 授权许可】

Unknown   

【 预 览 】
附件列表
Files Size Format View
RO201912020291573ZK.pdf 369KB PDF download
  文献评价指标  
  下载次数:18次 浏览次数:21次