Ishida Tetsuya, Hatae Tanenori, Nishi Nozomu, Araki Nobukazu
Department of Histology and Cell Biology, School of Medicine, Kagawa University, Miki, Kagawa 761-0793, Japan.
Cell Struct Funct. 2006;31(2):77-85. doi: 10.1247/csf.06013. Epub 2006 Oct 23.
The endolymphatic sac (ES) is believed to play an important role in maintaining homeostasis in the inner ear by the absorption and endocytosis of endolymph. Megalin is a 600-kDa multiligand endocytic receptor expressed in certain types of absorptive epithelia including kidney proximal tubules. We analyzed the immunoreactivity for megalin in rat ES by immunofluorescence, immunogold electron microscopy, and immunoblotting. With immunostaining, the luminal substances of the ES were strongly stained for megalin. Megalin was also localized in luminal macrophage-like cells and both types of epithelial cell (mitochondria-rich cells and ribosome-rich cells). In these cells, the megalin was localized in the lumen of endosomes, but was not membrane associated. This localization pattern indicates that the megalin in these cells is not a membrane receptor, but merely one of the constituents that are endocytosed from the lumen of the ES. Immunoblotting indicated that the megalin in the ES is a 210-kDa molecule lacking a cytoplasmic domain. This suggests that the megalin in the ES may be a soluble form, different from the 600-kDa membrane-bound receptor expressed in kidneys. Taken together, it is likely that the megalin in the ES lumen is a soluble component and may be endocytosed by the ES epithelial cells. Furthermore, we found that the tectorial membrane, an acellular structure in the cochlea, gave a strong megalin immunoreaction. Since the cochlea is connected to the ES, the megalin may be transported alone or with the components of the tectorial membrane from the cochlea to the ES lumen through longitudinal flow.
内淋巴囊(ES)被认为通过对内淋巴的吸收和胞吞作用在内耳稳态维持中发挥重要作用。巨膜蛋白是一种600 kDa的多配体胞吞受体,在包括肾近端小管在内的某些类型的吸收性上皮中表达。我们通过免疫荧光、免疫金电子显微镜和免疫印迹分析了大鼠内淋巴囊中巨膜蛋白的免疫反应性。免疫染色显示,内淋巴囊的管腔物质被巨膜蛋白强烈染色。巨膜蛋白也定位于管腔巨噬细胞样细胞以及两种类型的上皮细胞(富含线粒体的细胞和富含核糖体的细胞)中。在这些细胞中,巨膜蛋白定位于内体腔中,但不与膜相关。这种定位模式表明,这些细胞中的巨膜蛋白不是膜受体,而仅仅是从内淋巴囊管腔中被胞吞的成分之一。免疫印迹表明,内淋巴囊中的巨膜蛋白是一个缺乏细胞质结构域的210 kDa分子。这表明内淋巴囊中的巨膜蛋白可能是一种可溶性形式,不同于在肾脏中表达的600 kDa膜结合受体。综上所述,内淋巴囊管腔中的巨膜蛋白可能是一种可溶性成分,并且可能被内淋巴囊上皮细胞胞吞。此外,我们发现耳蜗中的一种无细胞结构——盖膜,呈现出强烈的巨膜蛋白免疫反应。由于耳蜗与内淋巴囊相连,巨膜蛋白可能单独或与盖膜成分一起通过纵向流动从耳蜗转运至内淋巴囊管腔。