A role for hyaluronan in macrophage accumulation and collagen deposition after bleomycin-induced lung injury

被引:66
作者
Savani, RC
Hou, GP
Liu, P
Wang, C
Simons, E
Grimm, PC
Stern, R
Greenberg, AH
DeLisser, HM
Khalil, N
机构
[1] Univ Penn, Dept Pediat, Div Neonatol, Philadelphia, PA 19104 USA
[2] Univ Penn, Pulm Allergy & Crit Care Div, Dept Med, Philadelphia, PA 19104 USA
[3] Univ Manitoba, Dept Pediat, Winnipeg, MB R3T 2N2, Canada
[4] Univ Manitoba, Dept Med, Winnipeg, MB R3T 2N2, Canada
[5] Univ Manitoba, Manitoba Inst Cell Biol, Winnipeg, MB R3T 2N2, Canada
[6] Univ Calif San Francisco, Dept Pathol, San Francisco, CA USA
关键词
D O I
10.1165/ajrcmb.23.4.3944
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Elevated concentrations of hyaluronan (HA) are associated with the accumulation of macrophages in the lung after injury. We have investigated the role of HA in the inflammatory and fibrotic responses to lung injury using the intratracheal instillation of bleomycin in rats as a model. After bleomycin-induced lung injury, both HA content in bronchoalveolar lavage (BAL) and staining for HA in macrophages accumulating in injured areas of the lung were maximal at 4 d. Increased HA in BAL correlated with increased locomotion of isolated alveolar macrophages. HA-binding peptide was able to specifically block macrophage motility in vitro. Importantly, systemic administration of HA-binding peptide to rats before injury not only decreased alveolar macrophage motility and accumulation in the lung, but also reduced lung collagen alpha (I) messenger RNA and hydroxyproline contents. We propose a model in which HA plays a critical role in the inflammatory response and fibrotic consequences of acute lung injury.
引用
收藏
页码:475 / 484
页数:10
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