Roles of CC chemokine receptors (CCRs) on lipopolysaccharide-induced acute lung injury

被引:21
作者
Yang, Dong [1 ]
Tong, Lin [1 ]
Wang, Diane [1 ]
Wang, Yaoli [1 ]
Wang, Xiangdong [1 ]
Bai, Chunxue [1 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Pulm Med, Shanghai, Peoples R China
关键词
CC chemokine receptor; Acute lung injury; Inflammation; Lipopolysaccharide (LPS); Plasminogen activator inhibitor (PAI)-1; RESPIRATORY-DISTRESS-SYNDROME; INDUCED NEUTROPHIL CHEMOATTRACTANT; ACUTE-PANCREATITIS; RECRUITMENT; PROTECTS; ENDOTOXEMIA; EXPRESSION; CELLS; MODEL;
D O I
10.1016/j.resp.2010.02.002
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The aim of the present study was to evaluate the effects of the CC chemokine receptor (CCR) 2b and CCR1 antagonist RS504393 as well as the roles of CCRs on lipopolysaccharide (LPS)-induced acute lung injury (ALI). In A549 cell line, treatment with RS504393 significantly inhibited the expression of CCR1. CCR2 and interleukin (IL)-8 after either LPS or tumor necrosis factor-a stimulation. An ALI model with intranasal LPS administration was used on C57BL/6J, CCR1, CCR2 and CCR3 knockout mice. Treatment with RS504393 had a noteworthy preventative effect on LPS-induced over-expression of IL-1 beta, plasminogen activator inhibitor and CCR2. In CCR1 and CCR2-deficient animals, LPS-induced less increase of lung weight, bronchoalveolar lavage (BAL) leukocytes and IL-6 compared to the C57BL/6J and CCR3 knockout mice. This was most prominent in the CCR2 knockout mice where no LPS-induced lung edema and no increase of IL-6 in BAL fluid occurred. Our results indicate that CCR2, and to some extent CCR1, play pivotal roles in the development of ALI. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:253 / 259
页数:7
相关论文
共 24 条
  • [1] Tolerance develops in spinal cord, but not in brain with chronic [Dmt1]DALDA treatment
    Ben, Y
    Smith, AP
    Schiller, PW
    Lee, NM
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2004, 143 (08) : 987 - 993
  • [2] Bhatia M., 2002, Current Drug Targets - Inflammation and Allergy, V1, P343
  • [3] Role of inflammatory mediators in the pathophysiology of acute respiratory distress syndrome
    Bhatia, M
    Moochhala, S
    [J]. JOURNAL OF PATHOLOGY, 2004, 202 (02) : 145 - 156
  • [4] Treatment with neutralising antibody against cytokine induced neutrophil chemoattractant (CINC) protects rats against acute pancreatitis associated lung injury
    Bhatia, M
    Brady, M
    Zagorski, J
    Christmas, SE
    Campbell, F
    Neoptolemos, JP
    Slavin, J
    [J]. GUT, 2000, 47 (06) : 838 - 844
  • [5] Expression of the chemokines MCP-1/JE and cytokine-induced neutrophil chemoattractant in early acute pancreatitis
    Brady, M
    Bhatia, M
    Christmas, S
    Boyd, MT
    Neoptolemos, JP
    Slavin, J
    [J]. PANCREAS, 2002, 25 (03) : 260 - 269
  • [6] Chemokine receptor CCR2 is expressed by human multiple myeloma cells and mediates migration to bone marrow stromal cell-produced monocyte chemotactic proteins MCP-1,-2 and-3
    Broek, IV
    Asosingh, K
    Vanderkerken, K
    Straetmans, N
    Van Camp, B
    Van Riet, I
    [J]. BRITISH JOURNAL OF CANCER, 2003, 88 (06) : 855 - 862
  • [7] Epidemiology and outcome of acute lung injury in European intensive care units - Results from the ALIVE study
    Brun-Buisson, C
    Minelli, C
    Bertolini, G
    Brazzi, L
    Pimentel, J
    Lewandowski, K
    Bion, J
    Rornand, JA
    Villar, J
    Thorsteinsson, A
    Damas, P
    Armaganidis, A
    Lemaire, FO
    [J]. INTENSIVE CARE MEDICINE, 2004, 30 (01) : 51 - 61
  • [8] Treatment with BX471, a nonpeptide CCR1 antagonist, protects mice against acute pancreatitis-associated lung injury by neutrophil recruitment
    He, Min
    Horuk, Richard
    Bhatia, Madhav
    [J]. PANCREAS, 2007, 34 (02) : 233 - 241
  • [9] MOLECULAR-PROPERTIES OF THE CHEMOKINE RECEPTOR FAMILY
    HORUK, R
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 1994, 15 (05) : 159 - 165
  • [10] CCR2+ monocyte-derived dendritic cells and exudate macrophages produce influenza-induced pulmonary immune pathology and mortality
    Lin, Kaifeng Lisa
    Suzuki, Yasushi
    Nakano, Hideki
    Ramsburg, Elizabeth
    Gunn, Michael Dee
    [J]. JOURNAL OF IMMUNOLOGY, 2008, 180 (04) : 2562 - 2572