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S100P是镉诱导抑制人胎盘滋养层细胞增殖的潜在分子靶点。

S100P is a potential molecular target of cadmium-induced inhibition of human placental trophoblast cell proliferation.

作者信息

Zhou Taimei, Wang Haiying, Zhang Shen, Jiang Xinglin, Wei Xiaolong

机构信息

Department of Medical Laboratory, Hunan University of Medicine, Huaihua 418000, China.

Department of Pathology, Cancer Hospital of Shantou University Medical College, Shantou 515031, China.

出版信息

Exp Toxicol Pathol. 2016 Nov;68(10):565-570. doi: 10.1016/j.etp.2016.09.002. Epub 2016 Sep 21.

Abstract

Cadmium, a common and highly toxic pollutant, has been known to accumulate high concentrations in placenta with deleterious effects on placental structure and function. Cadmium inhibits cell proliferation in placenta via targeting metal binding proteins. S100P, a Ca-binding protein, plays an important role in promoting cell proliferation and our previous study found its downregulation was linked to cadmium exposure in Guiyu, a famous e-waste recycling town in China. So, the present study was aimed to define whether cadmium inhibited cell proliferation through interfering with S100P. Using human trophoblast-derived HTR-8/SVneo cells as a model in vitro, we showed that cadmium exposure led to decreases in both cell proliferation and S100P expression. Knockdown of S100P in HTR-8/SVneo cells led to an obvious decrease of cell proliferation, and upregulation of S100P resulted in a significant increase of cell proliferation. Furthermore, after 24h of exposure to cadmium (20μM), cells transfected with pcDNA3.1-S100P showed a 1.3-fold higher S100P protein level, 38% higher proliferation evaluated with MTT assay than cells with no transfection, indicating that S100P expression attenuated cadmium-induced inhibition of cell proliferation. Taken together, we demonstrate that cadmium inhibits S100P expression and cell proliferation in placenta, meanwhile, S100P expression affects cell proliferation. Thus, our study is the first to indicate that cadmium may induce inhibition of placental trophoblast cell proliferation through targeting S100P.

摘要

镉是一种常见且剧毒的污染物,已知其会在胎盘中蓄积高浓度,对胎盘结构和功能产生有害影响。镉通过靶向金属结合蛋白抑制胎盘细胞增殖。S100P是一种钙结合蛋白,在促进细胞增殖中起重要作用,我们之前的研究发现其下调与中国著名电子垃圾回收镇贵屿的镉暴露有关。因此,本研究旨在确定镉是否通过干扰S100P来抑制细胞增殖。我们以人滋养层来源的HTR-8/SVneo细胞作为体外模型,结果表明镉暴露导致细胞增殖和S100P表达均下降。在HTR-8/SVneo细胞中敲低S100P导致细胞增殖明显减少,而S100P的上调则导致细胞增殖显著增加。此外,在暴露于镉(20μM)24小时后,用pcDNA3.1-S100P转染的细胞显示S100P蛋白水平高出1.3倍,用MTT法评估的增殖比未转染的细胞高38%,表明S100P表达减轻了镉诱导的细胞增殖抑制。综上所述,我们证明镉抑制胎盘细胞中S100P的表达和细胞增殖,同时,S100P表达影响细胞增殖。因此,我们的研究首次表明镉可能通过靶向S100P诱导胎盘滋养层细胞增殖抑制。

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