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异硫氰酸烯丙酯可增强人支气管上皮细胞系中多药耐药相关蛋白1(MRP1)的功能及表达。

Allyl isothiocyanate increases MRP1 function and expression in a human bronchial epithelial cell line.

作者信息

Wang Dian-lei, Wang Chen-yin, Cao Yin, Zhang Xian, Tao Xiu-hua, Yang Li-li, Chen Jin-pei, Wang Shan-shan, Li Ze-geng

机构信息

Anhui University of Chinese Medicine, Hefei, Anhui 230038, China.

The Fourth People's Hospital of Hefei, Hefei, Anhui 230022, China.

出版信息

Oxid Med Cell Longev. 2014;2014:547379. doi: 10.1155/2014/547379. Epub 2014 Jan 14.

Abstract

Multidrug resistance-associated protein 1 (MRP1), a member of the ATP-binding cassette (ABC) superfamily of transporters, plays an important role in normal lung physiology by protecting cells against oxidative stress and toxic xenobiotics. The present study investigates the effects of allyl isothiocyanate (AITC) on MRP1 mRNA and MRP1 protein expression and transporter activity in the immortalised human bronchial epithelial cell line 16HBE14o-. MRP1 mRNA and MRP1 protein expression in 16HBE14o- cells that were treated with allyl isothiocyanate were analysed by real-time PCR assay and Western blotting. The transport of carboxyfluorescein, a known MRP1 substrate, was measured by functional flow cytometry to evaluate MRP1 activity. Treatment with AITC at concentrations of 5-40 μM increased MRP1 protein levels in a concentration-dependent manner. AITC treatments at concentrations of 1-40 μM caused concentration-dependent increases in MRP1 mRNA levels that were up to seven times greater than the levels found in control cells. Finally, AITC treatment at concentrations of 5-40 μM significantly increased MRP1-dependent efflux in 16HBE14o- cells. These results suggest that AITC can increase the expression and activity of MRP1 in 16HBE14o- cells in a concentration-dependent manner. The upregulation of MRP1 activity and expression by AITC could produce therapeutic effects in the treatment of lung disease.

摘要

多药耐药相关蛋白1(MRP1)是ATP结合盒(ABC)转运蛋白超家族的成员之一,通过保护细胞免受氧化应激和有毒外源性物质的影响,在正常肺生理中发挥重要作用。本研究调查了异硫氰酸烯丙酯(AITC)对永生化人支气管上皮细胞系16HBE14o-中MRP1 mRNA和MRP1蛋白表达以及转运蛋白活性的影响。通过实时PCR分析和蛋白质印迹法分析了用异硫氰酸烯丙酯处理的16HBE14o-细胞中的MRP1 mRNA和MRP1蛋白表达。通过功能流式细胞术测量已知的MRP1底物羧基荧光素的转运,以评估MRP1活性。用5-40μM浓度的AITC处理以浓度依赖性方式增加了MRP1蛋白水平。1-40μM浓度的AITC处理导致MRP1 mRNA水平呈浓度依赖性增加,最高可达对照细胞中水平的7倍。最后,5-40μM浓度的AITC处理显著增加了16HBE14o-细胞中MRP1依赖性外排。这些结果表明,AITC可以以浓度依赖性方式增加16HBE14o-细胞中MRP1的表达和活性。AITC对MRP1活性和表达的上调可能在肺部疾病治疗中产生治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3e6/3942196/100b11762289/OMCL2014-547379.001.jpg

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