Department of Physiology and Pharmacology, University of Calgary, Calgary, Alberta T2N 4N1, Canada; email:
Snyder Institute for Chronic Diseases, Cumming School of Medicine, University of Calgary, Calgary, Alberta T2N 4N1, Canada.
Annu Rev Pathol. 2020 Jan 24;15:493-518. doi: 10.1146/annurev-pathmechdis-012419-032847. Epub 2019 Nov 1.
Recognizing the importance of leukocyte trafficking in inflammation led to some therapeutic breakthroughs. However, many inflammatory pathologies remain without specific therapy. This review discusses leukocytes in the context of sterile inflammation, a process caused by sterile (non-microbial) molecules, comprising damage-associated molecular patterns (DAMPs). DAMPs bind specific receptors to activate inflammation and start a highly optimized sequence of immune cell recruitment of neutrophils and monocytes to initiate effective tissue repair. When DAMPs are cleared, the recruited leukocytes change from a proinflammatory to a reparative program, a switch that is locally supervised by invariant natural killer T cells. In addition, neutrophils exit the inflammatory site and reverse transmigrate back to the bloodstream. Inflammation persists when the program switch or reverse transmigration fails, or when the coordinated leukocyte effort cannot clear the immunostimulatory molecules. The latter causes inappropriate leukocyte activation, a driver of many pathologies associated with poor lifestyle choices. We discuss lifestyle-associated inflammatory diseases and their corresponding immunostimulatory lifestyle-associated molecular patterns (LAMPs) and distinguish them from DAMPs.
认识到白细胞迁移在炎症中的重要性导致了一些治疗突破。然而,许多炎症性病理仍然没有特定的治疗方法。这篇综述讨论了无菌炎症中的白细胞,这是一种由无菌(非微生物)分子引起的过程,包括损伤相关分子模式(DAMPs)。DAMPs 结合特定的受体来激活炎症,并启动中性粒细胞和单核细胞的免疫细胞募集的高度优化的序列,以启动有效的组织修复。当 DAMPs 被清除时,募集的白细胞从促炎状态转变为修复状态,这种转变由不变自然杀伤 T 细胞在局部进行监督。此外,中性粒细胞离开炎症部位并反向迁移回血液。当程序转换或反向迁移失败,或者协调的白细胞作用不能清除免疫刺激分子时,炎症就会持续存在。后者导致白细胞的不当激活,这是与不良生活方式选择相关的许多病理的驱动因素。我们讨论了与生活方式相关的炎症性疾病及其相应的免疫刺激生活方式相关分子模式(LAMPs),并将它们与 DAMPs 区分开来。