Pivotal role of CCR1-positive leukocytes in bleomycin-induced lung fibrosis in mice

被引:87
作者
Tokuda, A
Itakura, M
Onai, N
Kimura, H
Kuriyama, T
Matsushima, K
机构
[1] Univ Tokyo, Sch Med, Dept Mol Prevent Med, Bunkyo Ku, Tokyo 1130033, Japan
[2] Chiba Univ, Sch Med, Dept Chest Med, Chiba 280, Japan
关键词
D O I
10.4049/jimmunol.164.5.2745
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have investigated the involvement of chemokine receptor CCR1-positive cells in bleomycin-induced lung injury, a model of pulmonary fibrosis. After bleomycin challenge in C57BL/6J mice, the expression of CCR1 mRNA increased and peaked at day 7, which paralleled to the expression of its ligands, macrophage-inflammatory protein-1 alpha and RANTES, Immunohistochemical study showed that CCR1-positive cells accumulated in the interstitial inflammatory site. Furthermore, the treatment of anti-CCR1 Ab significantly reduced the accumulation of inflammatory cells and collagen deposition, resulting in dramatic improvement of survival. These results suggest that CCR1-positive cells play significant roles in the pathogenesis of pulmonary fibrosis subsequent to bleomycin-induced lung injury, and that CCR1 could be a novel molecular target for intervention therapy against pulmonary fibrosis.
引用
收藏
页码:2745 / 2751
页数:7
相关论文
共 31 条
[1]   Chemokines and leukocyte traffic [J].
Baggiolini, M .
NATURE, 1998, 392 (6676) :565-568
[2]   Blocking chemokine receptors [J].
Baggiolini, M ;
Moser, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (08) :1189-1191
[3]   Eosinophil chemotactic activity in bronchoalveolar lavage from idiopathic pulmonary fibrosis is dependent on cytokine priming of eosinophils [J].
Boomars, KA ;
Schweizer, RC ;
Zanen, P ;
van den Bosch, JMM ;
Lammers, JWJ ;
Koenderman, L .
EUROPEAN RESPIRATORY JOURNAL, 1998, 11 (05) :1009-1014
[4]   Impaired host defense, hematopoiesis, guanulomatous inflammation and type 1-type 2 cytokine balance in mice lacking CC chemokine receptor 1 [J].
Gao, JL ;
Wynn, TA ;
Chang, Y ;
Lee, EJ ;
Broxmeyer, HE ;
Cooper, S ;
Tiffany, HL ;
Westphal, H ;
KwonChung, J ;
Murphy, PM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (11) :1959-1968
[5]   Targeted disruption of the beta-chemokine receptor CCR1 protects against pancreatitis-associated lung injury [J].
Gerard, C ;
Frossard, JL ;
Bhatia, M ;
Saluja, A ;
Gerard, NP ;
Lu, B ;
Steer, M .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (08) :2022-2027
[6]   EFFECT OF ANTIBODY TO TRANSFORMING GROWTH-FACTOR-BETA ON BLEOMYCIN-INDUCED ACCUMULATION OF LUNG COLLAGEN IN MICE [J].
GIRI, SN ;
HYDE, DM ;
HOLLINGER, MA .
THORAX, 1993, 48 (10) :959-966
[7]   Identification and characterization of small molecule functional antagonists of the CCR1 chemokine receptor [J].
Hesselgesser, J ;
Ng, HP ;
Liang, M ;
Zheng, W ;
May, K ;
Bauman, JG ;
Monahan, S ;
Islam, I ;
Wei, GP ;
Ghannam, A ;
Taub, DD ;
Rosser, M ;
Snider, RM ;
Morrissey, MM ;
Perez, HD ;
Horuk, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (25) :15687-15692
[8]  
Keane MP, 1999, J IMMUNOL, V162, P5511
[9]   Expression of RANTES by bronchoalveolar lavage cells in nonsmoking patients with interstitial lung diseases [J].
Kodama, N ;
Yamaguchi, E ;
Hizawa, N ;
Furuya, K ;
Kojima, J ;
Oguri, M ;
Takahashi, T ;
Kawakami, Y .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1998, 18 (04) :526-531
[10]   Defects in macrophage recruitment and host defense in mice lacking the CCR2 chemokine receptor [J].
Kurihara, T ;
Warr, G ;
Loy, J ;
Bravo, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (10) :1757-1762