| Project/Area Number |
22791611
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
Otorhinolaryngology
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| Research Institution | Kumamoto University |
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Principal Investigator |
ISE Momoko 熊本大学, 医学部附属病院, 医員 (20573596)
|
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| Co-Investigator(Renkei-kenkyūsha) |
MINODA Ryosei 熊本大学, 医学部付属病院, 准教授 (30284772)
MIWA Toru 熊本大学, 医学部付属病院, 医員 (70535591)
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| Project Period (FY) |
2010 – 2012
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| Project Status |
Completed (Fiscal Year 2012)
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| Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2012: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2011: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2010: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
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| Keywords | 再生医学 / ラセン神経節細胞 / PC3 / 神経突起 / ＰＣ３ / ラセン神経節 |
|---|
| Research Abstract |
Little is known about the detailed mechanism of the spiral ganglioncells(SGCs) of the rat cochlea developmental process. However, we reported that PC3 isinvolved in the shift from proliferation to differentiation and maturation in the SGCsof rat cochlea. In this study, we intend to make a clear relation between PC3 and thedifferentiation and maturation by examining the effect of suppressed expression of PC3using the isolation SGCs introduced PC3.siRNA. We observed the morphologic change of theSGCs which occurred because of suppressed expression of PC3 protein, after introducingPC3.siRNA into the SGCs and having cultured the cells for three days. However, there wasno significant morphologic change of the SGCs compared with control group.
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