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海洋毒素与细胞骨架:pectenotoxins,一类破坏肌动蛋白的特殊大环内酯类毒素

Marine toxins and the cytoskeleton: pectenotoxins, unusual macrolides that disrupt actin.

作者信息

Espiña Begoña, Rubiolo Juan A

机构信息

Departamento de Farmacologia, Facultad de Veterinaria, Universidad de Santiago de Compostela, Lugo, Spain.

出版信息

FEBS J. 2008 Dec;275(24):6082-8. doi: 10.1111/j.1742-4658.2008.06714.x. Epub 2008 Oct 24.

DOI:10.1111/j.1742-4658.2008.06714.x
PMID:19016860
Abstract

In recent years, many natural macrolactones have been found that display toxicity against the actin cytoskeleton. Pectenotoxins are macrolactones produced by species of the dinoflagellate genus Dinophysis. They were initially classified within the diarrheic shellfish poisoning group of toxins, because of their co-occurrence and biological origin, but mice toxicity assays demonstrated that pectenotoxins do not induce diarrheic symptoms. Intraperitoneal injection of pectenotoxins into mice produces high hepatotoxicity as the principal symptom, so the liver seems to be their target organ. Up to now, 15 pectenotoxin analogs have been discovered, with different toxicological potencies that are related to their structures. Now, it is generally accepted that the actin cytoskeleton is the principal molecular target of pectenotoxins. Although recent studies have demonstrated that pectenotoxins induce actin filament disruption by a capping effect, other kinds of activity, such as sequestration of actin, cannot be ruled out. All of the active analogs tested triggered disruption of the actin cytoskeleton and displayed potencies that correlated with their toxicity in mice. Moreover, pectenotoxins induce apoptosis to a higher degree in tumor cells than in normal cells of the same tissue. This fact opens the prospect of studying new chemotherapy agents and actin cytoskeleton dynamics with potential clinical applications.

摘要

近年来,人们发现许多天然大环内酯类化合物对肌动蛋白细胞骨架具有毒性。pectenotoxins是由双鞭毛藻属Dinophysis物种产生的大环内酯类化合物。由于它们的共同存在和生物学来源,它们最初被归类为腹泻性贝类中毒毒素组,但小鼠毒性试验表明pectenotoxins不会引发腹泻症状。将pectenotoxins腹腔注射到小鼠体内会产生以高肝毒性为主的症状,因此肝脏似乎是它们的靶器官。到目前为止,已发现15种pectenotoxin类似物,它们具有与其结构相关的不同毒理学效力。现在,人们普遍认为肌动蛋白细胞骨架是pectenotoxins的主要分子靶点。尽管最近的研究表明pectenotoxins通过封端效应诱导肌动蛋白丝破坏,但不能排除其他类型的活性,如肌动蛋白的螯合。所有测试的活性类似物均引发肌动蛋白细胞骨架的破坏,并显示出与其在小鼠中的毒性相关的效力。此外,pectenotoxins在肿瘤细胞中比在同一组织的正常细胞中诱导更高程度的细胞凋亡。这一事实为研究具有潜在临床应用的新型化疗药物和肌动蛋白细胞骨架动力学开辟了前景。

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