McKee C M, Penno M B, Cowman M, Burdick M D, Strieter R M, Bao C, Noble P W
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
J Clin Invest. 1996 Nov 15;98(10):2403-13. doi: 10.1172/JCI119054.
Hyaluronan (HA) is a glycosaminoglycan constituent of extracellular matrix. In its native form HA exists as a high molecular weight polymer, but during inflammation lower molecular weight fragments accumulate. We have identified a collection of inflammatory genes induced in macrophages by HA fragments but not by high molecular weight HA. These include several members of the chemokine gene family: macrophage inflammatory protein-1alpha, macrophage inflammatory protein-1beta, cytokine responsive gene-2, monocyte chemoattractant protein-1, and regulated on activation, normal T cell expressed and secreted. HA fragments as small as hexamers are capable of inducing expression of these genes in a mouse alveolar macrophage cell line, and monoclonal antibody to the HA receptor CD44 completely blocks binding of fluorescein-labeled HA to these cells and significantly inhibits HA-induced gene expression. We also investigated the ability of HA fragments to induce chemokine gene expression in human alveolar macrophages from patients with idiopathic pulmonary fibrosis and found that interleukin-8 mRNA is markedly induced. These data support the hypothesis that HA fragments generated during inflammation induce the expression of macrophage genes which are important in the development and maintenance of the inflammatory response.
透明质酸(HA)是细胞外基质的一种糖胺聚糖成分。在其天然形式下,HA以高分子量聚合物的形式存在,但在炎症过程中,低分子量片段会积累。我们已经鉴定出一组由HA片段而非高分子量HA在巨噬细胞中诱导产生的炎症基因。这些基因包括趋化因子基因家族的几个成员:巨噬细胞炎性蛋白-1α、巨噬细胞炎性蛋白-1β、细胞因子反应性基因-2、单核细胞趋化蛋白-1以及活化调节正常T细胞表达和分泌因子。小至六聚体的HA片段能够在小鼠肺泡巨噬细胞系中诱导这些基因的表达,并且针对HA受体CD44的单克隆抗体完全阻断了荧光素标记的HA与这些细胞的结合,并显著抑制了HA诱导的基因表达。我们还研究了HA片段在特发性肺纤维化患者的人肺泡巨噬细胞中诱导趋化因子基因表达的能力,发现白细胞介素-8 mRNA明显被诱导。这些数据支持了这样一种假说,即炎症过程中产生的HA片段诱导巨噬细胞基因的表达,而这些基因在炎症反应的发展和维持中起着重要作用。