Matrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington.
Comparative Pathology Program, Department of Comparative Medicine, University of Washington School of Medicine, Seattle, Washington.
J Histochem Cytochem. 2018 Apr;66(4):241-259. doi: 10.1369/0022155417751880. Epub 2018 Jan 12.
Proteoglycans (PGs) are complex, multifaceted molecules that participate in diverse interactions vital for physiological and pathological processes. As structural components, they provide a scaffold for cells and structural organization that helps define tissue architecture. Through interactions with water, PGs enable molecular and cellular movement through tissues. Through selective ionic interactions with growth factors, chemokines, cytokines, and proteases, PGs facilitate the ability of these soluble ligands to regulate intracellular signaling events and to influence the inflammatory response. In addition, recent findings now demonstrate that PGs can activate danger-associated molecular patterns (DAMPs) and other signaling pathways to influence production of many of these soluble ligands, indicating a more direct role for PGs in influencing the immune response and tissue inflammation. This review will focus on PGs that are selectively expressed during lung inflammation and will examine the novel emerging concept of PGs as immunomodulatory regulators of the innate immune responses in lungs.
蛋白聚糖(PGs)是复杂的、多方面的分子,参与多种对生理和病理过程至关重要的相互作用。作为结构成分,它们为细胞和结构组织提供了一个支架,有助于定义组织架构。通过与水的相互作用,PGs 使分子和细胞能够在组织中移动。通过与生长因子、趋化因子、细胞因子和蛋白酶的选择性离子相互作用,PGs 促进了这些可溶性配体调节细胞内信号事件和影响炎症反应的能力。此外,最近的发现表明,PGs 可以激活危险相关分子模式(DAMPs)和其他信号通路,以影响许多这些可溶性配体的产生,这表明 PGs 在影响免疫反应和组织炎症方面发挥着更直接的作用。这篇综述将集中讨论在肺部炎症期间选择性表达的 PGs,并研究 PGs 作为肺部固有免疫反应的免疫调节调节剂的新出现概念。