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  2. Endosulfan promotes cell migration via PTP4A3-mediated signaling pathways in HUVECs

Endosulfan promotes cell migration via PTP4A3-mediated signaling pathways in HUVECs

  • Ecotoxicol Environ Saf. 2020 Apr 1;192:110267. doi: 10.1016/j.ecoenv.2020.110267.
Heng Li 1 Shiqi Liu 2 Yumeng Hu 3 Bin Zhao 4 Yeqing Sun 5 Dan Xu 6
Affiliations

Affiliations

  • 1 Institute of Environmental Systems Biology, Dalian Maritime University, Linghai Road 1, Dalian, 116026, China. Electronic address: 458121092@qq.com.
  • 2 Institute of Environmental Systems Biology, Dalian Maritime University, Linghai Road 1, Dalian, 116026, China. Electronic address: 459778744@qq.com.
  • 3 Institute of Environmental Systems Biology, Dalian Maritime University, Linghai Road 1, Dalian, 116026, China. Electronic address: 759429332@qq.com.
  • 4 State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Shuangqing Road 18, Beijing, 100085, China. Electronic address: binzhao@rcees.ac.cn.
  • 5 Institute of Environmental Systems Biology, Dalian Maritime University, Linghai Road 1, Dalian, 116026, China. Electronic address: yqsun@dlmu.edu.cn.
  • 6 Institute of Environmental Systems Biology, Dalian Maritime University, Linghai Road 1, Dalian, 116026, China. Electronic address: jotan1995@163.com.
Abstract

Endosulfan is a persistent organic pollutant and can cause endothelial dysfunction, closely related to cardiovascular diseases. Endothelial cell migration plays a critical role in atherosclerosis and angiogenesis. This study was aimed to investigate the effect of environmentally relevant doses of endosulfan and underlying molecular mechanism on endothelial cell migration. Human umbilical vein endothelial cells (HUVECs) were treated with DMSO (control) or endosulfan (0.1, 1, 10 and 20 μM) in the presence or absence of inhibitors. Wound healing and Transwell assay were employed to explore the effect of endosulfan on endothelial cell migration. The expression of genes or proteins was assayed by Real-Time PCR or immunoblotting. The results showed that endosulfan at relative low concentration (0.1, 1, 10 and 20 μM) increased cell migration ability horizontally and vertically at 12 h after exposure. In line with this cellular effect, Protein-tyrosine Phosphatase 4A3 (PTP4A3) expression was significantly increased in endosulfan-exposed endothelial cells. Specific inhibitor of PTP4A3 significantly inhibited 20 μM endosulfan-induced cell migration, the expression and phosphorylation of Src and phosphorylation of focal adhesion kinase (FAK). Exposure to endosulfan resulted in activation of various signaling pathways including phosphoinositide 3-kinase (PI3K)/Akt, mitogen-activated protein kinase (MAPK) and nuclear factor kappa B (NF-κB), which were suppressed by PTP4A3 inhibitor or specific inhibitor for each signaling pathway. Exposure to endosulfan significantly reduced nitric oxide production and caused oxidative stress in HUVECs. These findings suggest that endosulfan promoted cell migration through PTP4A3-mediated various signaling pathways in endothelial cells.

Keywords

Cell migration; Endosulfan; Endothelial cells; PTP4A3; Signaling pathway.

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