真菌代谢物 altersolanol a 在体外通过线粒体介导的细胞凋亡对人胎盘滋养细胞具有强大的细胞毒性。

IF 2.6 4区 医学 Q2 MYCOLOGY Mycotoxin Research Pub Date : 2024-08-01 Epub Date: 2024-05-08 DOI:10.1007/s12550-024-00539-0
Ting Gu, Yuting Wen, Qian Zhou, Wei Yuan, Haichun Guo, Wen-Lin Chang, Qing Yang
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引用次数: 0

摘要

Altersolanol A 是一种从真菌中提取的四氢蒽醌,对多种癌细胞具有细胞毒性作用。然而,它对人类的生殖毒性尚未得到很好的研究。本研究旨在体外研究 altersolanol A 对人类胎盘滋养层细胞(包括绒毛膜癌细胞系 JEG-3 和正常滋养层细胞系 HTR-8/SVneo)的细胞毒性。结果表明,altersolanol A 可抑制人滋养细胞的增殖和集落形成,绒毛膜癌细胞对该化合物的敏感性高于正常滋养细胞。Altersolanol A 能诱导 JEG-3 细胞的细胞周期停滞在 G2/M 期,HTR-8/SVneo 细胞的细胞周期停滞在 S 期,下调细胞周期相关检查点蛋白的表达,并上调 p21 水平。土荆皮酚 A 还能通过提高 Bax/Bcl-2 比率、降低 caspase-3 和 caspase-9 水平来促进人滋养细胞的凋亡。同时,altersolanol A 可抑制线粒体膜电位,诱导 ROS 生成和细胞色素 c 释放,从而激活线粒体介导的内在凋亡。此外,暴露于 altersolanol A 后,JEG-3 细胞的基质金属蛋白酶(MMP)-2 和 HTR-8/SVneo 细胞的 MMP-9 下调,从而抑制了细胞的迁移和侵袭。从机理上讲,补充 altersolanol A 可降低 JNK、ERK 和 p38 的磷酸化,从而表明人滋养细胞中的 MAPK 信号通路失活。总之,altersolanol A 通过促进线粒体介导的细胞凋亡和抑制 MAPK 信号通路,对人类滋养细胞具有潜在的生殖细胞毒性。
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Fungal metabolite altersolanol a exhibits potent cytotoxicity against human placental trophoblasts in vitro via mitochondria-mediated apoptosis.

Altersolanol A, a fungus-derived tetrahydroanthraquinone, has shown cytotoxic effects on multiple cancer cells. However, its reproductive toxicity in humans has not been well-addressed. The present study was aimed at investigating the cytotoxicity of altersolanol A on human placental trophoblasts including choriocarcinoma cell line JEG-3 and normal trophoblast cell line HTR-8/SVneo in vitro. The results showed that altersolanol A inhibited proliferation and colony formation of human trophoblasts, and the choriocarcinoma cells were more sensitive to the compound than the normal trophoblasts. Altersolanol A induced cell cycle arrest at G2/M phase in JEG-3 cells and S phase in HTR-8/SVneo cells, downregulated the expression of cell cycle-related checkpoint proteins, and upregulated the p21 level. Altersolanol A also promoted apoptosis in human trophoblasts via elevating the Bax/Bcl-2 ratio and decreasing both caspase-3 and caspase-9 levels. Meanwhile, altersolanol A suppressed the mitochondrial membrane potential and induced ROS production and cytochrome c release, which activated the mitochondria-mediated intrinsic apoptosis. Moreover, migration and invasion were inhibited upon altersolanol A exposure with downregulation of matrix metalloproteinase (MMP)-2 in JEG-3 cells and MMP-9 in HTR-8/SVneo cells. Mechanically, altersolanol A supplement decreased the phosphorylation of JNK, ERK, and p38, manifesting the inactivation of MAPK signaling pathway in the human trophoblasts. In conclusion, altersolanol A exhibited potential reproductive cytotoxicity against human trophoblasts via promoting mitochondrial-mediated apoptosis and inhibiting the MAPK signaling pathway.

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来源期刊
Mycotoxin Research
Mycotoxin Research MYCOLOGYTOXICOLOGY-TOXICOLOGY
CiteScore
6.40
自引率
6.70%
发文量
29
期刊介绍: Mycotoxin Research, the official publication of the Society for Mycotoxin Research, is a peer-reviewed, scientific journal dealing with all aspects related to toxic fungal metabolites. The journal publishes original research articles and reviews in all areas dealing with mycotoxins. As an interdisciplinary platform, Mycotoxin Research welcomes submission of scientific contributions in the following research fields: - Ecology and genetics of mycotoxin formation - Mode of action of mycotoxins, metabolism and toxicology - Agricultural production and mycotoxins - Human and animal health aspects, including exposure studies and risk assessment - Food and feed safety, including occurrence, prevention, regulatory aspects, and control of mycotoxins - Environmental safety and technology-related aspects of mycotoxins - Chemistry, synthesis and analysis.
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