Nishimura T, Nakano T
Department of Anatomy, Aichi Medical University, Yazako, Japan.
Cell Struct Funct. 2000 Jun;25(3):161-9. doi: 10.1247/csf.25.161.
Through observations of colloidal gold with silver enhancement, we have demonstrated that 2-nm colloidal gold labeled-testosterone-bovine serum albumin (BSA) conjugate or hydrocortisone-BSA conjugate injected intravenously enters the hormone-target cell nuclei of rats (Nishimura and Ichihara, 1997; Nishimura and Nakano, 1997, 1999). To confirm immunocytochemically whether the nature of BSA in the steroid hormone-BSA conjugates (steroid-BSAs) remains intact in the hormone-target cell nuclei, testosterone-BSA, hydrocortisone-BSA or corticosterone-BSA was injected into the vascular system of rats, then the liver and testes of rats killed 2 h postinjection were reacted with FITC-conjugated anti-BSA antibody, and examined under fluorescence microscopy and confocal laser scanning microscopy. In the liver of rat injected with testosterone-BSA, the fluorescence was observed in the nuclei of endothelial cells, but not in the nuclei of hepatocytes, hepatic stellate cells and Kupffer cells. In the liver of rat injected with hydrocortisone-BSA, intense fluorescence was seen in the nuclei of hepatic stellate cells, but did not seem to be present in the nuclei of the other three kinds of cells. In the liver of rat injected with corticosterone-BSA, the fluorescence seemed to be in a few nuclei of hepatic stellate cells, and appeared as speckles in a few nuclei of the hepatocytes and Kupffer cells. In some seminiferous tubules of rat injected with testosterone-BSA, fluorescence was observed in the nuclei of spermatocytes and spermatids. These results suggest that BSA conjugated with steroid hormone can enter the hormone-target cell nuclei with its antigenicity kept intact, and that the fate of steroid-BSAs is decided at the cell membrane level.
通过对银增强胶体金的观察,我们已经证明静脉注射2纳米胶体金标记的睾酮 - 牛血清白蛋白(BSA)偶联物或氢化可的松 - BSA偶联物可进入大鼠的激素靶细胞核(西村和市原,1997;西村和中野,1997,1999)。为了通过免疫细胞化学方法确认类固醇激素 - BSA偶联物(类固醇 - BSAs)中的BSA性质在激素靶细胞核中是否保持完整,将睾酮 - BSA、氢化可的松 - BSA或皮质酮 - BSA注入大鼠的血管系统,然后在注射后2小时处死大鼠,取其肝脏和睾丸与异硫氰酸荧光素(FITC)偶联的抗BSA抗体反应,并在荧光显微镜和共聚焦激光扫描显微镜下检查。在注射睾酮 - BSA的大鼠肝脏中,在内皮细胞核中观察到荧光,但在肝细胞、肝星状细胞和库普弗细胞核中未观察到。在注射氢化可的松 - BSA的大鼠肝脏中,在肝星状细胞核中观察到强烈荧光,但在其他三种细胞的核中似乎不存在。在注射皮质酮 - BSA的大鼠肝脏中,荧光似乎存在于少数肝星状细胞核中,并在少数肝细胞核和库普弗细胞核中呈斑点状出现。在注射睾酮 - BSA的大鼠的一些生精小管中,在精母细胞和精子细胞核中观察到荧光。这些结果表明,与类固醇激素偶联的BSA可以以其完整的抗原性进入激素靶细胞核,并且类固醇 - BSAs的命运在细胞膜水平上就已决定。