2019 Fiscal Year Final Research Report
An inhibition of Semaphorin 3A enhances axonal outgrowth and stroke recovery
Project/Area Number |
17K09764
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Neurology
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Research Institution | Juntendo University |
Principal Investigator |
Ueno Yuji 順天堂大学, 医学部, 准教授 (00349002)
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Project Period (FY) |
2017-04-01 – 2020-03-31
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Keywords | 脳梗塞 / セマフォリン3A / エクソソーム / microRNA / 軸索再生 |
Outline of Final Research Achievements |
In rats subjected to MCA occlusion, we administered a Semaphorin 3A inhibitor into the peri-infarct area from 7 to 21 days after occlusion. We found that phosphorylated NFH-immunoreactive axons were increased, GFAP-immunoreactive astrocytes were decreased, and functional recovery was promoted at 28 days after MCAO. In cultured neurons, the Semaphorin 3A inhibitor decreased Rnd1, increased R-Ras, which phosphorylates Akt and GSK-3β, selectively increased phosphorylated GSK-3β in axons, and thereby enhanced phosphorylated NFH-immunoreactive axons after OGD. In cultured astrocytes, the Semaphorin 3A inhibitor suppressed activation of astrocytes induced by OGD. Exosomes secreted from ischemic astrocytes treated with the Semaphorin 3A inhibitor regulated expression of microRNAs, and further promoted axonal elongation together with an increase of ptgds. GSK-3β+ and PTGDS+ neurons were robustly increased after treatment with the Semaphorin 3A inhibitor in the peri-infarct area.
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Free Research Field |
神経学
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Academic Significance and Societal Importance of the Research Achievements |
我々は軸索伸長阻害因子である Semaphorin3Aに着目し、脳梗塞再生治療の新たな分子標的として見出した。Semaphorin3A阻害薬は、脳梗塞後の神経細胞内情報伝達系を制御し、アストロサイトの活性化を抑制、軸索伸展効果を有するエクソソームを分泌する現象がみられた。今日では急性期治療が主体となっている脳梗塞治療において、Semaphorin3A阻害薬は慢性期神経再生や機能回復をターゲットとした脳梗塞新規治療薬となる可能性がある。脳梗塞患者のQOLを高めるという高い社会的ニーズに答えるのみならず、脳卒中医療を大きく変革させる治療薬となる可能性がある。
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