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

Cited 15 time in Web of Science Cited 16 time in Scopus
Authors
Jin, S. N.; Mun, G. H.; Lee, J. H.; Oh, C. S.; Kim, J.; Chung, Y. H.; Kang, J. S.; Kim, J. G.; Hwang, D. H.; Hwang, Y. I.; Shin, D. H.; Lee, W. J.
Issue Date
2005-12-17
Publisher
Wiley-Blackwell
Citation
Microsc Res Tech. 2005 Dec 15;68(6):360-7.
Keywords
AnimalsAscorbic Acid/*metabolismBiological TransportImmunohistochemistry/methodsOrganic Anion Transporters, Sodium-Dependent/*metabolismRatsRats, Sprague-DawleyRespiratory System/*metabolismSodium/*metabolismSymporters/*metabolismTrachea/cytology
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.
ISSN
1059-910X (Print)
Language
English
URI
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=16358281

http://hdl.handle.net/10371/22638
DOI
https://doi.org/10.1002/jemt.20255
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College of Medicine/School of Medicine (의과대학/대학원)Immunology (면역학전공)Journal Papers (저널논문_면역학전공)
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