Jin Shun Nu, Mun Ga Hee, Lee Ju Hyun, Oh Chang Seok, Kim Jaehyup, Chung Yoon Hee, Kang Jae Seung, Kim Joong-Gon, Hwang Douk-Ho, Hwang Young Il, Shin Dong Hoon, Lee Wang Jae
Department of Anatomy, Seoul National University College of Medicine, Seoul, Korea.
Microsc Res Tech. 2005 Dec 15;68(6):360-7. doi: 10.1002/jemt.20255.
As vitamin C (L-ascorbic acid, VC) is known to be essential for many enzymatic reactions, the study on the transport mechanism of VC through cytoplasmic membrane is crucial to understanding physiological role of VC in cells and the respiratory system. In this regard, the study on the newly identified sodium-dependent VC transporters (SVCTs), SVCT1 and SVCT2, is required in organs that contain high concentration of VC. We have shown the distribution of SVCT proteins in the respiratory system, which has been reported to be one of the organs with a high concentration of VC, using immunohistochemical techniques. In the present study, intense SVCT immunoreactivities (IRs) were mainly localized in the respiratory system epithelial cells. In the trachea, both SVCT1 and 2 were localized in the psuedostratified ciliated columnar epithelium. In the terminal bronchiole, SVCT1 and 2 IRs were mainly observed in the apical portion of the simple columnar epithelium. In addition, SVCT IRs was localized within the cell membrane of some alveolar cells, even though we could not identify the exact cell types. These results provide the first evidence that intense SVCT1 and 2 IRs were found in the apical portion of the respiratory epithelial cells, suggesting that SVCT proteins in the apical portion could transport the reduced form of VC included in the airway surface liquid into the respiratory epithelial cells.
由于维生素C(L-抗坏血酸,VC)对许多酶促反应至关重要,因此研究VC通过细胞质膜的转运机制对于理解VC在细胞和呼吸系统中的生理作用至关重要。在这方面,需要在含有高浓度VC的器官中研究新发现的钠依赖性VC转运体(SVCTs),即SVCT1和SVCT2。我们已经使用免疫组织化学技术显示了SVCT蛋白在呼吸系统中的分布,呼吸系统据报道是含有高浓度VC的器官之一。在本研究中,强烈的SVCT免疫反应性(IRs)主要定位于呼吸系统上皮细胞。在气管中,SVCT1和2都定位于假复层纤毛柱状上皮。在终末细支气管中,SVCT1和2的IRs主要在单层柱状上皮的顶端部分观察到。此外,尽管我们无法确定确切的细胞类型,但SVCT IRs定位于一些肺泡细胞的细胞膜内。这些结果提供了首个证据,即在呼吸道上皮细胞的顶端部分发现了强烈的SVCT1和2 IRs,表明顶端部分的SVCT蛋白可以将气道表面液体中所含的还原形式的VC转运到呼吸道上皮细胞中。