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伏马菌素 B1 影响人脐静脉内皮细胞的生物物理特性、迁移和细胞骨架结构。

Fumonisin B1 Affects the Biophysical Properties, Migration and Cytoskeletal Structure of Human Umbilical Vein Endothelial Cells.

机构信息

Key Laboratory of Biology and Medical Engineering, Immune Cells and Antibody Engineering Research Center of Guizhou Province, School of Basic Medical Sciences/School of Biology and Engineering, Guizhou Medical University, Guiyang, China.

Key Laboratory of Environmental Pollution Monitoring and Disease Control, Ministry of Education, Guizhou Medical University, Guiyang, China.

出版信息

Cell Biochem Biophys. 2020 Sep;78(3):375-382. doi: 10.1007/s12013-020-00923-4. Epub 2020 Jun 5.

Abstract

Fumonisin B1 (FB1) is an important mycotoxin in nature and is a serious threat to human and animal health, but its specific target and molecular mechanism of the toxicity and potential carcinogenicity remain unclear. In this study, we first detected the effects of FB1 on the cell viability, biophysical properties, migration ability, and reactive oxygen species (ROS) of human umbilical vein endothelial cells (HUVECs). Subsequently, changes in the cytoskeletal structure and its binding proteins were analyzed by immunofluorescence and real-time PCR, respectively. The results showed that FB1 could inhibit the viability of HUVECs in a dose-dependent manner. After treatment of HUVECs with FB1, the hypotonic resistance, cell surface charges, cell membrane fluidity, and migration ability were weakened, whereas the ROS levels were significantly increased. Moreover, the cytoskeletal structure of the HUVECs was significantly changed, and the mRNA expression of some important actin-binding proteins was altered. Therefore, this study revealed that FB1 can affect the migration and cytoskeletal structure of HUVECs, which provides a new perspective for further understanding the molecular mechanisms of FB1 toxicity.

摘要

伏马菌素 B1(FB1)是自然界中一种重要的真菌毒素,对人类和动物健康构成严重威胁,但它的毒性和潜在致癌性的具体靶点和分子机制仍不清楚。在本研究中,我们首先检测了 FB1 对人脐静脉内皮细胞(HUVEC)活力、生物物理特性、迁移能力和活性氧(ROS)的影响。随后,通过免疫荧光和实时 PCR 分别分析细胞骨架结构及其结合蛋白的变化。结果表明,FB1 可呈剂量依赖性抑制 HUVEC 活力。用 FB1 处理 HUVEC 后,其低渗抗性、细胞表面电荷、细胞膜流动性和迁移能力减弱,而 ROS 水平显著升高。此外,HUVEC 的细胞骨架结构发生显著改变,一些重要的肌动蛋白结合蛋白的 mRNA 表达发生改变。因此,本研究揭示了 FB1 可影响 HUVEC 的迁移和细胞骨架结构,为进一步了解 FB1 毒性的分子机制提供了新视角。

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