プロジェクトの詳細
研究開始時の研究の概要
Furthermore, I will evaluate the underlying mechanism of how CD206 deficient macrophages are challenging to develop LAMs, how CD206+ M2-like macrophages uptake free fatty acids (FFA) to become LAMs, and how miRNAs derived from LAMs-exosome suppress metabolic favorable genes to develop insulin resistance.
ステータス | アクティブ |
---|---|
有効開始/終了日 | 2024/04/01 → 2027/03/31 |
資金調達
- Japan Society for the Promotion of Science: ¥4,680,000
キーワード
- Mrc1
- M2 macrophage