Analysis of the tissue-specific molecular structure and the regulatory mechanism in morphogenesis by extracellular arylsulfatase
Project/Area Number |
22570067
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Morphology/Structure
|
Research Institution | Hiroshima University |
Principal Investigator |
NAKATSUBO Keiko (MITSUNAGA Keiko) 広島大学, 大学院・理学研究科, 助教 (40192760)
|
Co-Investigator(Kenkyū-buntansha) |
YASUMASU Shigeki 上智大学, 理工学部, 教授 (00222357)
|
Co-Investigator(Renkei-kenkyūsha) |
AKIMOTO Yoshihiro 杏林大学, 医学部, 准教授 (60184115)
|
Project Period (FY) |
2010 – 2012
|
Project Status |
Completed (Fiscal Year 2012)
|
Budget Amount *help |
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2012: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2011: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2010: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
|
Keywords | 細胞外基質 / アリールスルファターゼ / 分子環境 / 形態形成 / 発生 |
Research Abstract |
Immunohistochemical analysis using medaka arylsulfatase (Ars) antibodies revealed that extracellular distribution and colocalization with extracellular matrices of ArsA and ArsB were observed only in the restricted regions, such as on the luminal side of blood vessels, and in the cerebral ventricle, though they were ubiquitously synthesized. Knockdown analysis of Arses by using morpholino antisense oligonucleotides showed that ArsB is involved in morphogenesis during medaka development. These results suggest the possibility that the Arses function as novel components of extracellular matrices by constructing extracellular environment through circulatory systems during development.
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Report
(4 results)
Research Products
(15 results)