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来自棘冠海星(Acanthaster planci)毒液的平刺毒素I在A375.S2细胞中诱导与氧化和内质网应激相关的细胞毒性。

Plancitoxin I from the venom of crown-of-thorns starfish (Acanthaster planci) induces oxidative and endoplasmic reticulum stress associated cytotoxicity in A375.S2 cells.

作者信息

Lee Chi-Chiu, Hsieh Hernyi Justin, Hsieh Cheng-Hong, Hwang Deng-Fwu

机构信息

Department of Food Science and Center of Excellence for the Ocean, National Taiwan Ocean University. 2 Pei-Ning Road, Keelung 202, Taiwan, ROC.

Penghu Marine Biology Research Center, Fishery Research Institute, Council of Agriculture, Magong, Penghu 880, Taiwan, ROC.

出版信息

Exp Mol Pathol. 2015 Aug;99(1):7-15. doi: 10.1016/j.yexmp.2015.05.001. Epub 2015 May 4.

Abstract

The crown-of-thorns starfish Acanthaster planci is a venomous starfish whose venom provokes strong cytotoxicity. In the present study, the purified cytotoxic toxin of A. planci venom (CAV) was identified as plancitoxin I protein by mass spectrum analyses. This study aims to investigate the molecular mechanism underlying the cytotoxicity function of plancitoxin I by focusing on the oxidative stress, mitochondrial dysfunction and endoplasmic reticulum (ER) stress pathway in human melanoma A375.S2 cells. The results indicated that after being treated with CAV toxin, A375.S2 cells significantly decreased viability in a dose-dependent manner. The CAV was found to reduce the cellular antioxidant enzymes such as SOD and CAT, and there was a significant decrease in total thiol level and mtDNA integrity, and it enhanced the lipid peroxidation. In addition, CAV increased cytosolic Ca(2+) concentration, and enhanced the expression of the ER molecular chaperones GRP78 and CHOP in a dose-dependent manner. CAV significantly elevated the activity of caspase-3, -8 and -9, and reduced the ratio of Bcl-2/Bax. The cells exhibited apoptosis were determined by using propidium iodide (PI) staining of DNA fragmentation (sub-G1 peak). In summary, the results demonstrated that plancitoxin I inhibits the proliferation of A375.S2 cells through induction of oxidative stress, mitochondrial dysfunction and ER stress associated apoptosis.

摘要

刺冠海星(Acanthaster planci)是一种有毒海星,其毒液具有很强的细胞毒性。在本研究中,通过质谱分析将纯化的刺冠海星毒液细胞毒素(CAV)鉴定为刺冠毒素I蛋白。本研究旨在通过关注人黑色素瘤A375.S2细胞中的氧化应激、线粒体功能障碍和内质网(ER)应激途径,探讨刺冠毒素I细胞毒性功能的分子机制。结果表明,用CAV毒素处理后,A375.S2细胞的活力以剂量依赖性方式显著降低。发现CAV可降低细胞抗氧化酶如超氧化物歧化酶(SOD)和过氧化氢酶(CAT),总巯基水平和线粒体DNA完整性显著降低,脂质过氧化增强。此外,CAV增加了胞质Ca(2+)浓度,并以剂量依赖性方式增强了内质网分子伴侣GRP78和CHOP的表达。CAV显著提高了半胱天冬酶-3、-8和-9的活性,并降低了Bcl-2/Bax的比值。通过使用碘化丙啶(PI)染色检测DNA片段化(亚G1峰)来确定细胞凋亡情况。总之,结果表明刺冠毒素I通过诱导氧化应激、线粒体功能障碍和内质网应激相关的凋亡来抑制A375.S2细胞的增殖。

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