| Project/Area Number |
23590231
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Multi-year Fund |
|---|
| Section | 一般 |
|---|
| Research Field |
General anatomy (including Histology/Embryology)
|
|---|
| Research Institution | Kanazawa University |
|---|
Principal Investigator |
|
|---|
| Co-Investigator(Renkei-kenkyūsha) |
WAKAYAMA Tomohiko 金沢大学, 医学系, 准教授 (70305100)
MIYUKI Yamamoto 金沢大学, 医学系, 助教 (60139780)
NAKAYA Masaaki 金沢大学, 医学系, 助教 (70422095)
|
|---|
| Project Period (FY) |
2011 – 2013
|
| Project Status |
Completed (Fiscal Year 2013)
|
| Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2011: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
|
|---|
| Keywords | 細胞分化 / 組織形成 / 顎下腺 / 顆粒性導管 / アンドロゲン / アンドロゲン受容体 / 甲状腺ホルモン / 導管系 / 性差 / 受容体 / 唾液腺 / マウス |
|---|
| Research Abstract |
We examined the SMG of mice deficient of the androgen receptor (ARKO). The development of granular convoluted tubules (GCT) in ARKO male was as low as in control female. The administration of androgens had no effect, whereas the administration of thyroid hormone (T4) caused the conversion of striated duct cells into GCT cells in ARKO SMG. These results confirmed that GCT differentiation caused by androgens is dependent on the classical androgen receptor (AR), whereas that by T4 is independent of the AR. Analysis of the gene expression profiles in ARKO SMG revealed new GCT-specific genes as well as genes up-or down-regulated in the SMG by androgens without involvement of the classical AR.
|
