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Effect Of Tris-(2-chloroethyl)-phosphate (tcep) At Environmental Concentration On The Levels Of Cell Cycle Regulatory Protein Expression In Primary Cultured Rabbit Renal Proximal Tubule Cells

机译:三(2-氯乙基)磷酸酯(tcep)在环境浓度下对原代培养兔肾近端小管细胞中细胞周期调控蛋白表达水平的影响

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Tris-(2-chloroethyl)-phosphate (TCEP) is a typical organophosphate flame retardant and has been designated as a micropollutant in aquatic environment. However, the potential effect of TCEP at environmental concentration is mostly unknown. Thus, the purpose of this study was to investigate the renal effect of TCEP at environmental concentration using primary cultured rabbit renal proximal tubule cells (PTCs). The results showed that TCEP at 10 mg L~(-1) decreased cell viability, 84.2% of the control, but increased lactate dehydroge-nase, 150% fold of the control. TCEP at 10 mg L~(-1) also inhibited expression of CDK4, cyclin D1, CDK2, and cyclin E (79.3%, 77.7%, 73.3%, and 67.8% of the control, respectively), but increased expression of p21~(WAF/Cip1) and p27~(Kip1) (167.7% and 141.3% of the control, respectively). TCEP decreased DNA synthesis and cell number, 77% and 70% of the control, respectively. Through study of cell viability, cell damage, cell cycle regulator expression, DNA synthesis and cell number, TCEP at 10 μg L~(-1) only affected the cells that TCEP increased expression of p21~(WAF/Cip1) and p27~(Kip1),118.6% and 121.5% of the control, respectively, but decreased DNA synthesis, 91.5% of the control. In conclusion, TCEP at 10 μg L~(-1) significantly increased cell cycle regulatory protein expression (p21~(WAF/Cip1) and p27~(Kip1)), but slightly decreased DNA synthesis in primary cultured rabbit renal PTCs.
机译:三(2-氯乙基)磷酸酯(TCEP)是一种典型的有机磷酸酯阻燃剂,已被指定为水生环境中的微污染物。但是,在环境浓度下TCEP的潜在作用几乎是未知的。因此,本研究的目的是研究使用原代培养的兔肾近端肾小管细胞(PTC)在环境浓度下TCEP的肾脏作用。结果表明,TCEP 10 mg L〜(-1)降低了细胞活力,是对照组的84.2%,但是乳酸脱氢酶增加了,是对照组的150%。 TCEP在10 mg L〜(-1)时也抑制CDK4,cyclin D1,CDK2和cyclin E的表达(分别为对照的79.3%,77.7%,73.3%和67.8%),但增加p21〜的表达。 (WAF / Cip1)和p27〜(Kip1)(分别为对照的167.7%和141.3%)。 TCEP降低了DNA的合成和细胞数量,分别为对照的77%和70%。通过研究细胞活力,细胞损伤,细胞周期调节子表达,DNA合成和细胞数目,TCEP在10μgL〜(-1)时仅影响TCEP增加p21〜(WAF / Cip1)和p27〜( Kip1)分别为对照组的118.6%和121.5%,但DNA合成减少了对照组的91.5%。总之,TCEP在10μgL〜(-1)时可显着增加细胞周期调节蛋白的表达(p21〜(WAF / Cip1)和p27〜(Kip1)),但在原代培养的兔肾PTC中的DNA合成会略有下降。

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