Sinclair P, Frezza J, Sinclair J, Bement W, Haugen S, Healey J, Bonkovsky H
Veterans Administration Hospital, White River Junction, VT 05001.
Biochem J. 1989 Feb 15;258(1):237-45. doi: 10.1042/bj2580237.
This study investigated whether the same cytochrome P-450 (P-450) isoenzymes were inducible in cultures of chick-embryo hepatocytes as in the liver of chicken embryos. We purified two isoenzymes of cytochrome P-450 from the livers of 17-day-old-chick embryos: one of molecular mass approx. 50 kDa induced in vivo by the phenobarbital-like inducer glutethimide, and the second of approx. 57 kDa induced by 3-methylcholanthrene. Rabbit antiserum against the 50 kDa protein inhibited benzphetamine demethylase activity in hepatic microsomes (microsomal fractions) from glutethimide-treated chick embryo. Antiserum to the 57 kDa protein inhibited ethoxyresorufin de-ethylase activity in hepatic microsomes from methylcholanthrene-treated chick embryo. Cultured chick hepatocytes were treated with chemicals known to induce isoenzymes of P-450 in rodent liver. The induced P-450s were quantified spectrophotometrically and characterized by immunoblotting and enzyme assays. From these studies, chemical inducers were classified into three groups: (i) chemicals that induced a P-450 isoenzyme of 50 kDa and increased benzphetamine demethylase activity: glutethimide, phenobarbital, metyrapone, mephenytoin, ethanol, isopentanol, isobutanol, lindane, lysodren; (ii) chemicals that induced a P-450 isoenzyme of 57 kDa and increased ethoxyresorufin de-ethylase activity: 3-methylcholanthrene and 3,3',4,4'-tetrachlorobiphenyl; and (iii) the mono-alpha-substituted 2,3',4,4',5-pentabromobiphenyl, which induced both proteins and both activities. The immunochemical data showed that chick-embryo hepatocytes in culture retain the inducibility of glutethimide- and methylcholanthrene-induced isoenzymes of P-450 that are inducible in the liver of the chicken embryo.
本研究调查了鸡胚肝细胞培养物中细胞色素P-450(P-450)同工酶是否与鸡胚肝脏中的一样具有可诱导性。我们从17日龄鸡胚的肝脏中纯化了两种细胞色素P-450同工酶:一种分子量约为50 kDa,在体内由苯巴比妥样诱导剂格鲁米特诱导产生;另一种约为57 kDa,由3-甲基胆蒽诱导产生。针对50 kDa蛋白的兔抗血清抑制了格鲁米特处理的鸡胚肝脏微粒体(微粒体部分)中的苄非他明脱甲基酶活性。针对57 kDa蛋白的抗血清抑制了3-甲基胆蒽处理的鸡胚肝脏微粒体中的乙氧异羟肟酸脱乙基酶活性。用已知可在啮齿动物肝脏中诱导P-450同工酶的化学物质处理培养的鸡肝细胞。通过分光光度法定量诱导的P-450,并通过免疫印迹和酶测定对其进行表征。从这些研究中,化学诱导剂被分为三组:(i)诱导50 kDa的P-450同工酶并增加苄非他明脱甲基酶活性的化学物质:格鲁米特、苯巴比妥、美替拉酮、美芬妥因、乙醇、异戊醇、异丁醇、林丹、氯丹;(ii)诱导57 kDa的P-450同工酶并增加乙氧异羟肟酸脱乙基酶活性的化学物质:3-甲基胆蒽和3,3',4,4'-四氯联苯;(iii)单α-取代的2,3',4,4',5-五溴联苯,它诱导了两种蛋白和两种活性。免疫化学数据表明,培养的鸡胚肝细胞保留了在鸡胚肝脏中可诱导的格鲁米特和3-甲基胆蒽诱导的P-450同工酶的可诱导性。