S1Pに依存する2群の先天性リンパ性細胞の臓器間取引は宿主防御をサポートする
Yuefeng Huang1, Kairui Mao2, Xi Chen1
1Laboratory of Immunology, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Bethesda, MD 20892, USA.
まとめ
生まれながらのリンパ性細胞2型 (ILC2s) は,感染中に腸から肺のような他の組織に移行します. この移動は宿主の防御と組織修復を助け,適応免疫を補完します.
科学分野:
- 免疫学
- 細胞生物学
背景:
- 生まれながらのリンパ性細胞 (ILC) は宿主防御と組織ホメオスタシスに不可欠です.
- ILCは伝統的に組織在住とみなされ,感染時の移動能力の理解は限られていた.
研究 の 目的:
- 感染時のILC2の移動行動を調査する.
- ILC2が異なる組織部位を移動できるかどうかを判断する.
主な方法:
- インターレウキン25またはヘルミント誘発炎症のモデルを使用した.
- ILC2sの起源と移住を追跡した.
- ILC2の移行におけるスフィンゴシン1-リン酸 (S1P) の役割を調査した.
主要な成果:
- 炎症性ILC2は,腸内膜の静止中のILC2から発生する.
- ILC2sは,S1P媒介の化学作用によって,肺を含む外周組織に移動する.
- 移動するILC2sは,外周部における抗ヘルミント防御と組織修復に寄与する.
結論:
- ILC2は,感染中に遠くの組織に移動できる循環細胞です.
- この移動は適応性リンパ球の行動に並行し,最初の場所を超えて保護を拡張します.
- ILCは局所的および遠隔の組織保護を提供し,適応免疫を補完します.
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