Role of Chemokines in the Pathogenesis of Acute Lung Injury

被引:219
作者
Bhatia, Madhav [1 ]
Zemans, Rachel L. [2 ,3 ]
Jeyaseelan, Samithamby [4 ,5 ]
机构
[1] Univ Otago, Dept Pathol, Christchurch 8140, New Zealand
[2] Natl Jewish Hlth, Dept Med, Denver, CO USA
[3] Univ Colorado, Denver, CO 80202 USA
[4] Louisiana State Univ, Ctr Expt Infect Dis Res, Baton Rouge, LA 70803 USA
[5] Louisiana State Univ, Hlth Sci Ctr, New Orleans, LA USA
基金
美国国家卫生研究院;
关键词
acute lung injury; inflammation; leukocytes; experimental; clinical; RESPIRATORY-DISTRESS-SYNDROME; PULMONARY HOST-DEFENSE; MONOCYTE CHEMOATTRACTANT PROTEIN-1; INDUCED NEUTROPHIL CHEMOATTRACTANT; MACROPHAGE INFLAMMATORY PROTEIN-2; UP-REGULATES CYCLOOXYGENASE-2; ENDOTHELIAL PROGENITOR CELLS; PROSTAGLANDIN-E METABOLITE; KERATINOCYTE GROWTH-FACTOR; PUNCTURE-INDUCED SEPSIS;
D O I
10.1165/rcmb.2011-0392TR
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
Acute lung injury (ALI) is due to an uncontrolled systemic inflammatory response resulting from direct injury to the lung or indirect injury in the setting of a systemic process. Such insults lead to the systemic inflammatory response syndrome (SIRS), which includes activation of leukocytes-alveolar macrophages and sequestered neutrophils-in the lung. Although systemic inflammatory response syndrome is a physiologic response to an insult, systemic leukocyte activation, if excessive, can lead to end organ injury, such as ALI. Excessive recruitment of leukocytes is critical to the pathogenesis of ALI, and the magnitude and duration of the inflammatory process may ultimately determine the outcome in patients with ALI. Leukocyte recruitment is a well orchestrated process that depends on the function of chemokines and their receptors. Understanding the mechanisms that contribute to leukocyte recruitment in ALI may ultimately lead to the development of effective therapeutic strategies.
引用
收藏
页码:566 / 572
页数:7
相关论文
共 111 条
[41]   Treatment with BX471, a CC chemokine receptor 1 antagonist, attenuates systemic inflammatory response during sepsis [J].
He, Min ;
Horuk, Richard ;
Moochhala, Shabbir M. ;
Bhatia, Madhav .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2007, 292 (04) :G1173-G1180
[42]   ADMINISTRATION OF EXOGENOUS FRACTALKINE, A CX3C CHEMOKINE, IS CAPABLE OF MODULATING INFLAMMATORY RESPONSE IN CECAL LIGATION AND PUNCTURE-INDUCED SEPSIS [J].
He, Min ;
Moochhala, Shabbir M. ;
Adhikari, Sharmila ;
Bhatia, Madhav .
SHOCK, 2009, 31 (01) :33-39
[43]  
Horuk Richard, 2009, Front Biosci (Elite Ed), V1, P209
[44]   The chemokine receptor D6 limits the inflammatory response in vivo [J].
Jamieson, T ;
Cook, DN ;
Nibbs, RJB ;
Rot, A ;
Nixon, C ;
Mclean, P ;
Alcami, A ;
Lira, SA ;
Wiekowski, M ;
Graham, GJ .
NATURE IMMUNOLOGY, 2005, 6 (04) :403-411
[45]   Induction of CXCL5 during inflammation in the rodent lung involves activation of alveolar epithelium [J].
Jeyaseelan, S ;
Manzer, R ;
Young, SK ;
Yamamoto, M ;
Akira, S ;
Mason, RJ ;
Worthen, GS .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2005, 32 (06) :531-539
[46]   Transcriptional profiling of lipopolysaccharide-induced acute lung injury [J].
Jeyaseelan, S ;
Chu, HW ;
Young, SK ;
Worthen, GS .
INFECTION AND IMMUNITY, 2004, 72 (12) :7247-7256
[47]   Chronic inflammation upregulates chemokine receptors and induces neutrophil migration to monocyte chemoattractant protein-1 [J].
Johnston, B ;
Burns, AR ;
Suematsu, M ;
Issekutz, TB ;
Woodman, RC ;
Kubes, P .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (09) :1269-1276
[48]   CXCR2 Mediates the Recruitment of Endothelial Progenitor Cells During Allergic Airways Remodeling [J].
Jones, Carla P. ;
Pitchford, Simon C. ;
Lloyd, Clare M. ;
Rankin, Sara M. .
STEM CELLS, 2009, 27 (12) :3074-3081
[49]   A high endothelial venule-expressing promiscuous chemokine receptor DARC can bind inflammatory, but not lymphoid, chemokines and is dispensable for lymphocyte homing under physiological conditions [J].
Kashiwazaki, M ;
Tanaka, T ;
Kanda, H ;
Ebisuno, Y ;
Izawa, D ;
Fukuma, N ;
Akimitsu, N ;
Sekimizu, K ;
Monden, M ;
Miyasaka, M .
INTERNATIONAL IMMUNOLOGY, 2003, 15 (10) :1219-1227
[50]   Identification of bronchioalveolar stem cells in normal lung and lung cancer [J].
Kim, CFB ;
Jackson, EL ;
Woolfenden, AE ;
Lawrence, S ;
Babar, I ;
Vogel, S ;
Crowley, D ;
Bronson, RT ;
Jacks, T .
CELL, 2005, 121 (06) :823-835