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Blood Translation Elongation Factor-1δ Is a Novel Marker for Cadmium Exposure

机译:血液翻译延伸因子-1δ是镉暴露的新标记

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摘要

Translation elongation factor-1δ (TEF-1δ) has been identified as a novel cadmium-responsive proto-oncogene. However, it is still unclear whether TEF-1δ could be a potential biomarker of cadmium exposure. Rats were treated with CdCl2 at different concentrations (high dose 1.225, mid-dose 0.612 and low dose 0.306 mg/kg body weight, respectively) for 14 weeks, and the cadmium levels, weight coefficients, serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), blood urea nitrogen (BUN), serum creatinine (SCR), 24-h urine protein (24hPro), urinary creatinine (Cr) and pathological features were determined. The TEF-1δ expression in white blood cells and multiple organs were examined by reverse transcription polymerase chain reaction (PCR) and were also confirmed with fluorescence quantitative PCR. A cadmium dose-dependent increase (p < 0.05) of cadmium levels in blood, urine, liver, kidney, heart and lung, and the weight coefficients was observed. The liver and renal function indictors including AST, ALT, SCR, BUN and 24hPro, were elevated in a cadmium dose-dependent manner (p < 0.05). Significant pathological changes in liver, kidney, heart and lung were indicated. The TEF-1δ expression was up-regulated in both blood and organs (p < 0.05). Moreover, the expression level of blood TEF-1δ was positively correlated to TEF-1δ expression level, cadmium level and toxicity in the organs (p < 0.01). This study indicates that blood TEF-1δ is a novel valuable biomarker for cadmium exposure and its organ toxicity.
机译:翻译延伸因子-1δ(TEF-1δ)已被确定为一种新型的镉响应原癌基因。但是,尚不清楚TEF-1δ是否可能是镉暴露的潜在生物标记。用不同浓度(分别为高剂量1.225,中剂量0.612和低剂量0.306 mg / kg体重)的CdCl2处理大鼠,持续14周,以及镉水平,体重系数,血清丙氨酸氨基转移酶(ALT),天冬氨酸氨基转移酶(AST),血尿素氮(BUN),血清肌酐(SCR),24小时尿蛋白(24hPro),尿肌酐(Cr)和病理特征被确定。通过逆转录聚合酶链反应(PCR)检测白细胞和多个器官中的TEF-1δ表达,并通过荧光定量PCR进行确认。观察到血液,尿液,肝脏,肾脏,心脏和肺中镉的镉剂量依赖性增加(p <0.05),并观察到体重系数。肝和肾功能指标,包括AST,ALT,SCR,BUN和24hPro,以镉剂量依赖性方式升高(p <0.05)。指示肝,肾,心脏和肺的重大病理变化。在血液和器官中,TEF-1δ表达均上调(p <0.05)。此外,血液TEF-1δ的表达水平与器官中TEF-1δ的表达水平,镉水平和毒性呈正相关(p <0.01)。这项研究表明血液TEF-1δ是镉暴露及其器官毒性的一种新型有价值的生物标志物。

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