Zagon Ian S, Ruth Torre B, McLaughlin Patricia J
Department of Neural and Behavioral Sciences, Pennsylvania State University, College of Medicine, 500 University Drive, Rm. C3727, Hershey, PA 17033, USA.
Anat Rec A Discov Mol Cell Evol Biol. 2005 Jan;282(1):24-37. doi: 10.1002/ar.a.20161.
The subcellular distributions of the opioid growth factor (OGF), [Met(5)]-enkephalin, and opioid growth factor receptor (OGFr) in the epithelium of the rat tongue were determined in order to reveal structure-function relationships. Laser scanning confocal microscopic analysis showed that both OGF and OGFr were colocalized in the paranuclear cytoplasm and in the nuclei of keratinocytes in the stratum basale. Using immunoelectron microscopy and postembedding techniques, double labeling experiments disclosed that complexes of OGF-OGFr were colocalized on the outer nuclear envelope, in the paranuclear cytoplasm, perpendicular to the nuclear envelope in a putative nuclear pore complex, and in the nucleus adjacent to heterochromatin. Anti-OGF IgG alone was detected in the cytoplasm, and anti-OGFr IgG alone was associated with the outer nuclear envelope. Study of chronic treatment with the opioid antagonist, naltrexone (NTX), which blocks opioid-receptor binding, revealed the presence of OGFr immunoreactivity alone in the cytoplasm and the nucleus; some OGF-OGFr complexes were also observed. Colocalization of OGFr and karyopherin (importin) beta was recorded in the cytoplasm and nucleus. These results in tongue epithelium are the first to suggest that OGFr resides on the outer nuclear envelope, where OGF interacts with OGFr; that the OGF-OGFr complex translocates between cytoplasm and nucleus at the nuclear pore; and that the nuclear localization signal of OGFr interacts with karyopherin beta for nuclear transport. These novel data also indicate that signal transduction for cell proliferation appears to involve an OGF-OGFr complex that interfaces with chromatin in the nucleus. Moreover, the unique finding that OGFr was found in the cytoplasm and nucleus in NTX-treated specimens may suggest that NTX-OGFr complexes have the same pathway as OGF-OGFr.
为揭示结构-功能关系,测定了阿片样生长因子(OGF)、[Met(5)]-脑啡肽和阿片样生长因子受体(OGFr)在大鼠舌上皮中的亚细胞分布。激光扫描共聚焦显微镜分析显示,OGF和OGFr共定位于基底细胞层角质形成细胞的核周细胞质和细胞核中。利用免疫电子显微镜和包埋后技术,双重标记实验表明,OGF-OGFr复合物共定位于核外膜、核周细胞质、垂直于核膜的假定核孔复合体中以及与异染色质相邻的细胞核中。单独的抗OGF IgG在细胞质中被检测到,单独的抗OGFr IgG与核外膜相关。对阿片样拮抗剂纳曲酮(NTX)进行慢性治疗的研究显示,细胞质和细胞核中单独存在OGFr免疫反应性;还观察到一些OGF-OGFr复合物。在细胞质和细胞核中记录到OGFr与核转运蛋白(输入蛋白)β的共定位。舌上皮中的这些结果首次表明,OGFr位于核外膜上,OGF在此与OGFr相互作用;OGF-OGFr复合物在核孔处的细胞质和细胞核之间转运;OGFr的核定位信号与核转运蛋白β相互作用以进行核运输。这些新数据还表明,细胞增殖的信号转导似乎涉及与细胞核中的染色质相互作用的OGF-OGFr复合物。此外,在NTX处理的标本中,OGFr在细胞质和细胞核中被发现这一独特发现可能表明,NTX-OGFr复合物与OGF-OGFr具有相同的途径。