Gebhardt R, Fitzke H, Fausel M, Eisenmann-Tappe I, Mecke D
Physiologisch-chemisches Institut, Universität Tübingen, FRG.
Cell Biol Toxicol. 1990 Oct;6(4):365-78. doi: 10.1007/BF00120803.
GST activities against 1-Chloro-2,4-dinitrobenzene (CDNB) and 1,2-dichloro-4-nitrobenzene (DCNB) were measured in isolated and cultured adult rat hepatocytes. Within 24 h in culture, both GST activities decreased to about 70% and either stabilized at this level (CDNB) or recovered (DCNB) to the initial level. Use of hyaluronidase in addition to collagenase during the isolation of the cells strongly reduced both activities and its stimulation by various drugs for up to 168 h. The hormones insulin, glucagon, triiodothyronine, estradiol, testosterone, and progesterone did not affect GST activity, while dexamethasone showed some interference. In the presence of dexamethasone the activity against CDNB was mainly stimulated by the combination of methylcholanthrene (MC) and phenobarbital (PB) to about 260% within 168 h. The activity against DCNB was stimulated predominantly by MC alone reaching 170% after 168 h. Quantification of the GST subunits Ya, Yb1 and Yp by an ELISA technique revealed a strong decrease of Ya, a transient increase of Yb1 after 24 h followed by a moderate decrease, and a stable low level of the transformation marker Yp during cultivation. The level of Ya was markedly induced by PB, particularly in combination with MC. The level of Yb1 was equally induced by MC or PB with no synergistic effect. Yp was not affected by these drugs. None of the hormones affected the level of these GST subunits. These results indicate that the physiological type of regulation of the GSTs is maintained during primary culture and no signs of dedifferentiation or transformation are observed. Furthermore, they demonstrate that the interaction of drugs and hormones and their inducing potential can be efficiently studied in the cultured hepatocytes.
在分离培养的成年大鼠肝细胞中测定了谷胱甘肽S-转移酶(GST)对1-氯-2,4-二硝基苯(CDNB)和1,2-二氯-4-硝基苯(DCNB)的活性。在培养24小时内,两种GST活性均降至约70%,之后对CDNB的活性稳定在该水平,对DCNB的活性则恢复到初始水平。在细胞分离过程中,除胶原酶外还使用透明质酸酶,这会强烈降低两种活性及其受各种药物刺激长达168小时的程度。胰岛素、胰高血糖素、三碘甲状腺原氨酸、雌二醇、睾酮和孕酮等激素均不影响GST活性,而地塞米松有一定干扰作用。在地塞米松存在的情况下,对CDNB的活性主要在168小时内被甲基胆蒽(MC)和苯巴比妥(PB)联合刺激至约260%。对DCNB的活性主要由MC单独刺激,168小时后达到170%。通过酶联免疫吸附测定(ELISA)技术对GST亚基Ya、Yb1和Yp进行定量分析显示,Ya显著减少,Yb1在24小时后短暂增加,随后适度减少,培养期间转化标记物Yp维持在稳定的低水平。Ya的水平被PB显著诱导,特别是与MC联合时。Yb1的水平被MC或PB同等诱导,无协同效应。Yp不受这些药物影响。这些激素均不影响这些GST亚基的水平。这些结果表明,在原代培养过程中GST的生理调节类型得以维持,未观察到去分化或转化的迹象。此外,这些结果还表明,在培养的肝细胞中能够有效地研究药物与激素的相互作用及其诱导潜能。