Resolvin E1 and protectin D1 activate inflammation-resolution programmes

Jan M. Schwab, Nan Chiang, Makoto Arita, Charles N. Serhan

研究成果: Article査読

912 被引用数 (Scopus)

抄録

Resolution of acute inflammation is an active process essential for appropriate host responses, tissue protection and the return to homeostasis. During resolution, specific omega-3 polyunsaturated fatty-acid-derived mediators are generated within resolving exudates, including resolvin E1 (RvE1) and protectin D1 (PD1). It is thus important to pinpoint specific actions of RvE1 and PD1 in regulating tissue resolution. Here we report that RvE1 and PD1 in nanogram quantities promote phagocyte removal during acute inflammation by regulating leukocyte infiltration, increasing macrophage ingestion of apoptotic polymorphonuclear neutrophils in vivo and in vitro, and enhancing the appearance of phagocytes carrying engulfed zymosan in lymph nodes and spleen. In this tissue terrain, inhibition of either cyclooxygenase or lipoxygenases - pivotal enzymes in the temporal generation of both pro-inflammatory and pro-resolving mediators - caused a 'resolution deficit' that was rescued by RvE1, PD1 or aspirin-triggered lipoxin A4 analogue. Also, new resolution routes were identified that involve phagocytes traversing perinodal adipose tissues and non-apoptotic polymorphonuclear neutrophils carrying engulfed zymosan to lymph nodes. Together, these results identify new active components for postexudate resolution traffic, and demonstrate that RvE1 and PD1 are potent agonists for resolution of inflamed tissues.

本文言語English
ページ(範囲)869-874
ページ数6
ジャーナルNature
447
7146
DOI
出版ステータスPublished - 2007 6月 14
外部発表はい

ASJC Scopus subject areas

  • 一般

フィンガープリント

「Resolvin E1 and protectin D1 activate inflammation-resolution programmes」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル