Hyaluronan (HA) fragments induce chemokine gene expression in alveolar macrophages - The role of HA size and CD44

被引:674
作者
McKee, CM
Penno, MB
Cowman, M
Burdick, MD
Strieter, RM
Bao, C
Noble, PW
机构
[1] JOHNS HOPKINS UNIV, SCH MED, DIV PULM & CRIT CARE MED, DEPT MED, BALTIMORE, MD 21205 USA
[2] POLYTECH INST NEW YORK, DEPT CHEM, BROOKLYN, NY 11201 USA
[3] UNIV MICHIGAN, MED CTR, DEPT MED, ANN ARBOR, MI 48109 USA
关键词
extracellular matrix; interleukin-8; inflammation; proteoglycan; pulmonary fibrosis;
D O I
10.1172/JCI119054
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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-1 alpha, macrophage inflammatory protein-1 beta, 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.
引用
收藏
页码:2403 / 2413
页数:11
相关论文
共 66 条
[1]   HUMAN INTERFERON-INDUCIBLE PROTEIN-10 IS A POTENT INHIBITOR OF ANGIOGENESIS IN-VIVO [J].
ANGIOLILLO, AL ;
SGADARI, C ;
TAUB, DD ;
LIAO, F ;
FARBER, JM ;
MAHESHWARI, S ;
KLEINMAN, HK ;
REAMAN, GH ;
TOSATO, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (01) :155-162
[2]   CD44 IS THE PRINCIPAL CELL-SURFACE RECEPTOR FOR HYALURONATE [J].
ARUFFO, A ;
STAMENKOVIC, I ;
MELNICK, M ;
UNDERHILL, CB ;
SEED, B .
CELL, 1990, 61 (07) :1303-1313
[3]  
BAGGIOLINI M, 1994, ADV IMMUNOL, V55, P97
[4]   INTERACTION BETWEEN CD44 AND HYALURONATE IS DIRECTLY IMPLICATED IN THE REGULATION OF TUMOR-DEVELOPMENT [J].
BARTOLAZZI, A ;
PEACH, R ;
ARUFFO, A ;
STAMENKOVIC, I .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (01) :53-66
[5]  
BELITSOS PC, 1990, J IMMUNOL, V144, P1661
[6]   MECHANISMS OF PULMONARY FIBROSIS - SPONTANEOUS RELEASE OF THE ALVEOLAR MACROPHAGE-DERIVED GROWTH-FACTOR IN THE INTERSTITIAL LUNG DISORDERS [J].
BITTERMAN, PB ;
ADELBERG, S ;
CRYSTAL, RG .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 72 (05) :1801-1813
[7]   HYALURONAN AND TYPE-III PROCOLLAGEN PEPTIDE CONCENTRATIONS IN BRONCHOALVEOLAR LAVAGE FLUID IN IDIOPATHIC PULMONARY FIBROSIS [J].
BJERMER, L ;
LUNDGREN, R ;
HALLGREN, R .
THORAX, 1989, 44 (02) :126-131
[8]  
BOURGUIGNON LYW, 1993, J IMMUNOL, V151, P6634
[9]  
BUCHUJA S, 1980, INT J CANCER, V26, P171
[10]   INCREASED EXPRESSION OF THE INTERLEUKIN-8 GENE BY ALVEOLAR MACROPHAGES IN IDIOPATHIC PULMONARY FIBROSIS - A POTENTIAL MECHANISM FOR THE RECRUITMENT AND ACTIVATION OF NEUTROPHILS IN LUNG FIBROSIS [J].
CARRE, PC ;
MORTENSON, RL ;
KING, TE ;
NOBLE, PW ;
SABLE, CL ;
RICHES, DWH .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (06) :1802-1810