2023 Fiscal Year Final Research Report
Molecular mechanisms of IL1b-induced proliferation of synovial mesenchymal stroll cells
Project/Area Number |
21K16678
|
Research Category |
Grant-in-Aid for Early-Career Scientists
|
Allocation Type | Multi-year Fund |
Review Section |
Basic Section 56020:Orthopedics-related
|
Research Institution | Tokyo Medical and Dental University |
Principal Investigator |
Matsumura Etsuko 東京医科歯科大学, 大学院医歯学総合研究科, 非常勤講師 (30831854)
|
Project Period (FY) |
2021-04-01 – 2024-03-31
|
Keywords | MSC / IL1b / CD121a / Proliferation |
Outline of Final Research Achievements |
To efficiently provide regenerative therapy for articular cartilage using autologous synovial mesenchymal stem cells (MSCs), it is crucial to establish a protocol that ensures the safe and reliable supply of autologous cells for transplantation. However, due to inherent variability in the proliferative capacity of patient-derived cells, maintaining a consistently sufficient number of transplantable cells remains a challenge. Our research has demonstrated that IL-1β acts as a potent growth factor for MSC proliferation without compromising their differentiation capacity. However, the subset of IL-1β receptor-positive cells in MSCs is relatively low, approximately around 5%, suggesting the presence of unidentified IL-1β signaling pathways in MSCs. The aim of this study was to elucidate the molecular mechanisms underlying IL-1β-induced MSC proliferation and apply this knowledge to advance tissue regeneration therapies.
|
Free Research Field |
整形外科学
|
Academic Significance and Societal Importance of the Research Achievements |
本研究は、MSC特異的に存在するIL1b受容体を介したMSC増殖の新規分子メカニズムの解析を行うものであり、先行研究は存在しない。私たちのこれまでの研究成果から、MSCと炎症性細胞で異なるIL1bに対する細胞応答性が観察される原因として、異なる受容体アイソフォームの発現が考えられたが、このようなIL1b受容体の生理機能は今まで報告されておらず、本研究はIL-1bの新たなバイオロジーの開拓につながると考えている。
|