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Aroclor 1254 暴露对成骨细胞系 MC3T3-E1 的毒性作用及其分子机制。

The toxic effects of Aroclor 1254 exposure on the osteoblastic cell line MC3T3-E1 and its molecular mechanism.

机构信息

Institute of Environmental Pollution and Health, School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, PR China.

出版信息

Toxicology. 2012 May 16;295(1-3):8-14. doi: 10.1016/j.tox.2012.02.009. Epub 2012 Mar 3.

Abstract

Polychlorinated biphenyls (PCBs) are still prevalent in the environment despite the fact that they have been banned in many countries for several decades. Recent epidemiologic studies have demonstrated a link between PCBs exposure and pathological alterations of bone tissues. The aim of this study was to investigate the toxic effects of the PCBs mixture Aroclor 1254 on MC3T3-E1 preosteoblasts and explore the underlying molecular mechanism. Different doses of Aroclor 1254 were used to treat MC3T3-E1 and the cell viability, apoptosis, ALP activity, intracellular calcium (Ca2+) level and oxidative stress response were measured. The expression level of related proteins TRPV6, Apaf-1 and Bax was evaluated with Western blot assay. The subcellular distribution of TRPV6 protein was detected with immunofluorescence assay. The results indicated that the higher dose of Aroclor 1254 (>10 mg/L) could inhibit the cell proliferation and induce apoptosis in MC3T3-E1. The ROS level following Aroclor 1254 exposure was elevated with the concentration, while the ALP activity and intracellular calcium (Ca2+) level decreased. After Aroclor 1254 exposure, the expression level of calcium transport related protein TRPV6 was down-regulated, while the expression level of apoptosis related proteins Apaf-1 and Bax up-regulated in a dose dependant manner. The immunofluorescence assay results showed that the expression of TRPV6 in the cytoplasm was greatly suppressed after Aroclor 1254 exposure. In conclusion, Aroclor 1254 exposure could induce toxic effects in MC3T3-E1 as evidenced by inhibition of proliferation, induction of apoptosis and suppression of ALP activity. The ROS production and alteration of intracellular Ca2+ level induced by down-regulation of TRPV6 might involve the toxic effects, and cell apoptosis induced by Aroclor 1254 exposure is associated with the pro-apoptotic Apaf-1 pathway as well as alteration of Bcl-2/Bax ratio.

摘要

多氯联苯 (PCBs) 尽管在几十年前已被许多国家禁止使用,但在环境中仍普遍存在。最近的流行病学研究表明,PCBs 暴露与骨组织的病理改变之间存在关联。本研究旨在探讨多氯联苯混合物 Aroclor 1254 对 MC3T3-E1 前成骨细胞的毒性作用,并探讨其潜在的分子机制。用不同剂量的 Aroclor 1254 处理 MC3T3-E1,测量细胞活力、细胞凋亡、碱性磷酸酶 (ALP) 活性、细胞内钙离子 (Ca2+) 水平和氧化应激反应。用 Western blot 检测法评估相关蛋白 TRPV6、Apaf-1 和 Bax 的表达水平。用免疫荧光法检测 TRPV6 蛋白的亚细胞分布。结果表明,较高剂量的 Aroclor 1254(>10mg/L)可抑制 MC3T3-E1 的细胞增殖并诱导细胞凋亡。随着浓度的增加,Aroclor 1254 暴露后 ROS 水平升高,而 ALP 活性和细胞内钙离子 (Ca2+) 水平降低。Aroclor 1254 暴露后,钙转运相关蛋白 TRPV6 的表达水平下调,而凋亡相关蛋白 Apaf-1 和 Bax 的表达水平呈剂量依赖性上调。免疫荧光法结果显示,Aroclor 1254 暴露后,TRPV6 在细胞质中的表达受到很大抑制。综上所述,Aroclor 1254 暴露可引起 MC3T3-E1 的毒性作用,表现为增殖抑制、细胞凋亡诱导和 ALP 活性抑制。TRPV6 下调引起的 ROS 产生和细胞内 Ca2+ 水平改变可能涉及毒性作用,Aroclor 1254 暴露诱导的细胞凋亡与促凋亡 Apaf-1 途径以及 Bcl-2/Bax 比值的改变有关。

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