創傷治癒の鍵となる分子を特定(Key molecule in wound healing identified)

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2024-10-08 カロリンスカ研究所(KI)

カロリンスカ研究所と中国医学科学院の研究により、皮膚の創傷治癒に重要なRNA分子「SNHG26」が特定されました。この分子は炎症段階から修復段階への移行を導く役割を果たし、特に慢性創傷などで治癒を促進する可能性があります。マウス実験では、SNHG26の欠如が治癒を遅らせることが確認され、新たな治療法の開発が期待されています。研究は他のRNA分子の役割も調査し、難治性創傷への革新的な治療法を目指しています。

<関連情報>

lncRNAのSNHG26が創傷治癒におけるケラチノサイト前駆細胞の炎症状態から増殖状態への移行を促進する The lncRNA SNHG26 drives the inflammatory-to-proliferative state transition of keratinocyte progenitor cells during wound healing

Dongqing Li,Zhuang Liu,Letian Zhang,Xiaowei Bian,Jianmin Wu,Li Li,Yongjian Chen,Lihua Luo,Ling Pan,Lingzhuo Kong,Yunting Xiao,Jiating Wang,Xiya Zhang,Wang Wang,Maria Toma,Minna Piipponen,Pehr Sommar & Ning Xu Landén
Nature Communications  Published:05 October 2024
DOI:https://doi.org/10.1038/s41467-024-52783-8

創傷治癒の鍵となる分子を特定(Key molecule in wound healing identified)

Abstract

The cell transition from an inflammatory phase to a subsequent proliferative phase is crucial for wound healing, yet the driving mechanism remains unclear. By profiling lncRNA expression changes during human skin wound healing and screening lncRNA functions, we identify SNHG26 as a pivotal regulator in keratinocyte progenitors underpinning this phase transition. Snhg26-deficient mice exhibit impaired wound repair characterized by delayed re-epithelization accompanied by exacerbated inflammation. Single-cell transcriptome analysis combined with gain-of-function and loss-of-function of SNHG26 in vitro and ex vivo reveals its specific role in facilitating inflammatory-to-proliferative state transition of keratinocyte progenitors. A mechanistic study unravels that SNHG26 interacts with and relocates the transcription factor ILF2 from inflammatory genomic loci, such as JUN, IL6, IL8, and CCL20, to the genomic locus of LAMB3. Collectively, our findings suggest that lncRNAs play cardinal roles in expediting tissue repair and regeneration and may constitute an invaluable reservoir of therapeutic targets in reparative medicine.

有機化学・薬学
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