Derive Marc, Massin Frédéric, Gibot Sébastien
Groupe Choc; contrat Avenir INSERM; Faculté de Médecine; Nancy Université
Self Nonself. 2010 Jul;1(3):225-230. doi: 10.4161/self.1.3.12891. Epub 2010 Jul 2.
The Triggering Receptor Expressed on Myeloid cells (TREM)-1 is a recently identified molecule involved in monocytic activation and inflammatory response. It belongs to a family related to Natural Killer cell-receptors and is expressed on neutrophils, mature monocytes and macrophages. The engagement of TREM-1 synergizes with several Toll Like Receptors (TLR) and/or NOD Like Receptors (NLR) activation in amplifying the inflammatory response mediated by microbial components or danger signals. The implication of TREM-1 during experimental models of acute or chronic inflammatory conditions, as well as during cancer, begins to understand. Furthermore, the modulation of the TREM-1 signaling pathway by the use of small synthetic peptides derived from its extracellular moiety confers interesting survival advantages during experimental murine septic shock and protects from organ damage during other inflammatory diseases. This review summarizes the recent advances on TREM-1 biology and highlights the promises of its therapeutic modulation.
髓系细胞表达的触发受体(TREM)-1是一种最近发现的参与单核细胞活化和炎症反应的分子。它属于与自然杀伤细胞受体相关的家族,在中性粒细胞、成熟单核细胞和巨噬细胞上表达。TREM-1的激活与几种 Toll 样受体(TLR)和/或 NOD 样受体(NLR)的激活协同作用,放大由微生物成分或危险信号介导的炎症反应。TREM-1在急性或慢性炎症性疾病以及癌症实验模型中的作用开始被了解。此外,使用源自其细胞外部分的小合成肽对TREM-1信号通路进行调节,在实验性小鼠脓毒性休克期间具有有趣的生存优势,并在其他炎症性疾病中保护免受器官损伤。本综述总结了TREM-1生物学的最新进展,并强调了其治疗调节的前景。