Project/Area Number |
13671940
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Functional basic dentistry
|
Research Institution | The University of Tokushima |
Principal Investigator |
HOSOI Kazuo School of Dentistry, Professor, 歯学部, 教授 (10049413)
|
Co-Investigator(Kenkyū-buntansha) |
TSUMURA Keiko Faculty of Engineering Technical Official, 工学部, 教務員 (50127841)
AKAMATSU Tetsuya School of Dentistry, Research Associate, 歯学部, 助手 (80294700)
KANAMORI Norio School of Dentistry, Associate Professor, 歯学部, 助教授 (90064865)
多田 淳 徳島大学, 歯学部・附属病院, 医員
|
Project Period (FY) |
2001 – 2002
|
Project Status |
Completed (Fiscal Year 2002)
|
Budget Amount *help |
¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 2002: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 2001: ¥1,800,000 (Direct Cost: ¥1,800,000)
|
Keywords | aquaporins / trafficking / salivary gland / Sprague-Dawley rat / duodenum / Brunner's gland / genetic variation |
Research Abstract |
Localization of aquaporin 5 (AQP5) in the rat Brunner's gland and its regulation by vasoactive intestinal polypeptide (VIP) were in vestigated. Treatment of slices of duodenum with VIP in vitro for 2 or 7 min significantly increased amount of AQP5 in the duodenal apical membrane fraction. Intravenous injection of rats with VIP (40 ug/kg body weight) for 2 or 7 min provoked strong dilation of the lumen and increased the staining intensity of AQP5 in the apical and lateral membranes,whereas thae staining inside of the cells was appreciably reduced. AQP1 was also found to be localized in the apical and basolateral membranes of Brunner's gland; VIP however did not provoke any significant change in the AQP1 level in the apical membrane as judged from the results of the in vitro and vivo experiments. These results suggest that VIP induced the exocytosis of granule contents and simultanenously caused translocation of AQP5 to the apical membrane in the Brunner's gland. The expression level of aquapoin (AQP)5 in the submandibular gland (SMG) was found to be different among individual rats of the Sprague-Dawley (SD) straim. Such differences were observed for AQP5 but not for AQP1 and consequently the SD strain was divided into two groups, one expressing a high level of AQP5 and the other a low one. Breeding between brother and sister was repeated for two times within high expressers and low expressers to obtain the third generation progenies (F2); the AQP5 level of the SMG in the third generation (F2rats) from high expressers was significantly higher than the F2 from low expressers. Our present study suggests the existence of genetic variation in the expression of a water channel protein, AQP5, in rats.
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