Usuda N, Reddy M K, Hashimoto T, Rao M S, Reddy J K
Department of Pathology, Northwestern University Medical School, Chicago, Illinois.
Lab Invest. 1988 Jan;58(1):100-11.
The localization of urate oxidase in different tissues of rat and in the livers of selected mammalian species was investigated by immunoblot analysis and protein A-gold immunoelectron microscopy. Urate oxidase was purified from rat liver and used as an antigen to generate polyclonal antibodies in the rabbit. The antibodies were found to be monospecific by immunodiffusion and immunoblot analyses. By immunoblot analysis, urate oxidase was detected in the livers of rat, two strains of mice, hamster, dog, cat, and cow, but not in the Cynomolgus monkey and human liver. Urate oxidase was not detected by immunoblot method in rat kidney, jejunal mucosa, adrenal gland, testis, and pancreas. The subcellular localization of urate oxidase was ascertained by the protein A-gold immunocytochemical staining of the Lowicryl K4M embedded tissues. Urate oxidase was localized exclusively in the crystalloid core of the peroxisome in hepatic parenchymal cells of rat, mouse, hamster, dog, cat, and cow. The limiting membrane and the matrix of hepatic peroxisomes in these species were negative for the staining. The marginal plates of feline, canine, and bovine hepatic peroxisomes were also negative for urate oxidase. This enzyme was also not detected within the peroxisomes of human and monkey livers by the immunocytochemical technique. Peroxisomes (microperoxisomes) in extrahepatic rat tissues did not stain positively for urate oxidase by the protein A-gold immunocytochemical method, although they were positive for catalase. Fatty acyl-CoA oxidase was present in peroxisomes of jejunal mucosa, Leydig cells of test-is and pancreas but not in adrenal gland. Administration of a hepatic peroxisome proliferator, ciprofibrate or Wy-14643, failed to induce urate oxidase in rat liver. These results indicate that urate oxidase is a liver specific protein in rat and its localization within the liver peroxisomes of six mammals, excluding man and a nonhuman primate, and that its localization is limited exclusively to the crystalloid core. Unlike fatty acyl-CoA oxidase, urate oxidase does not appear to be inducible significantly by peroxisome proliferator treatment in the rat liver.
通过免疫印迹分析和蛋白A-金免疫电子显微镜技术,研究了尿酸氧化酶在大鼠不同组织以及所选哺乳动物肝脏中的定位。从大鼠肝脏中纯化尿酸氧化酶,并将其作为抗原在兔体内产生多克隆抗体。通过免疫扩散和免疫印迹分析发现这些抗体具有单特异性。通过免疫印迹分析,在大鼠、两种小鼠品系、仓鼠、狗、猫和牛的肝脏中检测到尿酸氧化酶,但在食蟹猴和人肝脏中未检测到。通过免疫印迹法在大鼠肾脏、空肠黏膜、肾上腺、睾丸和胰腺中未检测到尿酸氧化酶。通过对用Lowicryl K4M包埋的组织进行蛋白A-金免疫细胞化学染色来确定尿酸氧化酶的亚细胞定位。尿酸氧化酶仅定位于大鼠、小鼠、仓鼠、狗、猫和牛肝实质细胞过氧化物酶体的类晶体核心中。这些物种肝脏过氧化物酶体的界膜和基质染色呈阴性。猫、狗和牛肝脏过氧化物酶体的边缘板对尿酸氧化酶染色也呈阴性。通过免疫细胞化学技术在人和猴肝脏的过氧化物酶体中也未检测到这种酶。尽管大鼠肝外组织中的过氧化物酶体(微过氧化物酶体)对过氧化氢酶呈阳性,但通过蛋白A-金免疫细胞化学方法对尿酸氧化酶染色呈阴性。脂肪酰辅酶A氧化酶存在于空肠黏膜的过氧化物酶体、睾丸的Leydig细胞和胰腺中,但不存在于肾上腺中。给予肝脏过氧化物酶体增殖剂环丙贝特或Wy-14643未能在大鼠肝脏中诱导尿酸氧化酶。这些结果表明,尿酸氧化酶是大鼠肝脏中的一种特异性蛋白,其在六种哺乳动物(不包括人和一种非人类灵长类动物)肝脏过氧化物酶体中的定位,并且其定位仅限于类晶体核心。与脂肪酰辅酶A氧化酶不同,尿酸氧化酶在大鼠肝脏中似乎不会因过氧化物酶体增殖剂处理而显著诱导。