2020 Fiscal Year Final Research Report
Development of antiresorptive therapy targeting immunoglobulin-like receptors
Project/Area Number |
17H04309
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Orthopaedic surgery
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Research Institution | Hokkaido University |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
須田 廣美 (木村―須田) 公立千歳科学技術大学, 理工学部, 教授 (00574857)
古川 潤一 北海道大学, 医学研究院, 特任准教授 (30374193)
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Project Period (FY) |
2017-04-01 – 2021-03-31
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Keywords | 破骨細胞 / 骨吸収 / 免疫受容体 / 骨粗鬆症 / 骨破壊性疾患 / Siglec-15 |
Outline of Final Research Achievements |
While existing bone resorptive agents have a strong inhibitory effect on osteoclasts, they inhibit physiological bone resorption and bone growth by strongly suppressing bone metabolism and bone resorption in the bone growth plate. In this study, we conducted an exploratory study of therapeutic targets that selectively suppress pathological bone resorption without adversely affecting bone remodeling and bone growth. Among the immunoglobulin-like receptor molecules (IgLR) that are important for osteoclast differentiation and activation, Siglec-15 has a therapeutic effect on postmenopausal osteoporosis in which the bone remodeling balance is disturbed, and also on pediatric steroid-induced osteoporosis without causing growth disorders.
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Free Research Field |
整形外科学 骨代謝学
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Academic Significance and Societal Importance of the Research Achievements |
破骨細胞の分化や活性化に必須の免疫受容体チロシン活性化モチーフ(ITAM)依存性共刺激シグナル制御機構にはまだ不明な点が多い。本研究は、この経路を賦活化する複数の免疫受容体IgRLがそれぞれ異なる役割をもつことを示すとともに、その中でSiglec-15がもっとも重要な役割をもつことを明らかにした。Siglec-15は高齢者に生じる骨粗鬆症だけでなく、ステロイドや先天性疾患などによって生じる小児骨粗鬆症に対しても適応可能なきわめて有望な治療ターゲットであることを明らかにした。
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