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Immunohistochemical study on the distribution of sodium-dependent vitamin C transporters in the respiratory system of adult rat

Authors
Jin, SNMun, GHLee, JHOh, CSKim, JChung, YHKang, JSKim, JGHwang, DHHwang, YIShin, DHLee, WJ
Issue Date
Dec-2005
Publisher
WILEY-BLACKWELL
Keywords
vitamin C (L-ascorbic acid); sodium-dependent vitamin C transporters (SVCTs); rat; lung; trachea; bronchiole
Citation
MICROSCOPY RESEARCH AND TECHNIQUE, v.68, no.6, pp 360 - 367
Pages
8
Journal Title
MICROSCOPY RESEARCH AND TECHNIQUE
Volume
68
Number
6
Start Page
360
End Page
367
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24458
DOI
10.1002/jemt.20255
ISSN
1059-910X
1097-0029
Abstract
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.
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