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酸性鞘磷脂酶介导50赫兹磁场诱导的表皮生长因子受体在脂筏上聚集。

Acid sphingomyelinase mediates 50-Hz magnetic field-induced EGF receptor clustering on lipid raft.

作者信息

Wang Yong, Li Xingwen, Sun Liyuan, Feng Baihuan, Sun Wenjun

机构信息

a Bioelectromagnetics Key Laboratory, Zhejiang University School of Medicine , Hangzhou , Zhejiang , People's Republic of China.

b Cixi Sanitary Supervision Station , Cixi , People's Republic of China.

出版信息

J Recept Signal Transduct Res. 2016 Dec;36(6):593-600. doi: 10.3109/10799893.2016.1147583. Epub 2016 Feb 26.

DOI:10.3109/10799893.2016.1147583
PMID:26915736
Abstract

Previously, we found that exposure to a 50-Hz magnetic field (MF) could induce epidermal growth factor receptor (EGFR) clustering and phosphorylation on cell surface. In order to explore the possible mechanisms, the roles of acid sphingomyelinase (ASMase) and lipid raft in MF-induced EGFR clustering were investigated in the present study. Human amnion epithelial (FL) cells were exposed to a 50-Hz MF at 0.4 mT for different durations. Intracellular ASMase activity was detected using the Amplex® Red Sphingomyelinase Assay Kit. EGFR clustering, ASMase, and lipid rafts on cell membrane were analyzed using confocal microscopy after indirect immunofluorescence staining. Results showed that disturbing lipid rafts with nystatin could inhibit MF-induced EGFR clustering, indicating that it was dependent on intact lipid raft. Exposure of FL cells to MF significantly enhanced ASMase activity and induced ASMase translocation to membrane that co-localized with lipid rafts. Treatment with imipramine, an ASMase inhibitor, inhibited the MF-induced EGFR clustering. This inhibitory effect could be blocked by the addition of C2-ceramide in the culture medium. It suggested that ASMase mediated the 50-Hz MF-induced EGFR clustering via ceramide which was produced from hydrolyzation on lipid rafts.

摘要

此前,我们发现暴露于50Hz的磁场(MF)可诱导表皮生长因子受体(EGFR)在细胞表面聚集和磷酸化。为了探究其可能的机制,本研究调查了酸性鞘磷脂酶(ASMase)和脂筏在MF诱导的EGFR聚集中的作用。将人羊膜上皮(FL)细胞暴露于0.4mT的50Hz MF下不同时长。使用Amplex® Red鞘磷脂酶检测试剂盒检测细胞内ASMase活性。间接免疫荧光染色后,用共聚焦显微镜分析细胞膜上的EGFR聚集、ASMase和脂筏。结果显示,用制霉菌素扰乱脂筏可抑制MF诱导的EGFR聚集,表明其依赖于完整的脂筏。将FL细胞暴露于MF可显著增强ASMase活性,并诱导ASMase转位至与脂筏共定位的细胞膜上。用ASMase抑制剂丙咪嗪处理可抑制MF诱导的EGFR聚集。在培养基中添加C2-神经酰胺可阻断这种抑制作用。这表明ASMase通过在脂筏上水解产生的神经酰胺介导50Hz MF诱导的EGFR聚集。

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