Additional functions for the cysteinyl leukotrienes recognized through studies of inflammatory processes in null strains

被引:11
作者
Austen, K. Frank [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Rheumatol Immunol & Allergy,Dept Med, Boston, MA 02115 USA
关键词
cysteinyl leukotrienes; chronic inflammatory cell responses; adaptive immune response; SLOW-REACTING SUBSTANCE; INDUCED PULMONARY-FIBROSIS; GENE DISRUPTION REVEALS; ANAPHYLAXIS SRS-A; HUMAN MAST-CELLS; C-4; SYNTHASE; MOLECULAR-CLONING; VASCULAR-PERMEABILITY; NUCLEAR-ENVELOPE; GUINEA-PIG;
D O I
10.1016/j.prostaglandins.2007.01.004
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
Until recently, the cysteinyl leukotrienes, initially termed, slow reacting substance of anaphylaxis, were viewed entirely as effectors of smooth muscle constriction of bronchial airways to impair air flow and of microvasculature to evoke a plasma leak. The development of mice with targeted disruption of the synthesis of the cysteinyl leukotrienes or of their receptor-mediated action has within the last 5 years uncovered new functions in chronic inflammation and in regulation of the adaptive immune response. As innate host responses precede antigen presentation and then follow antigen specific recognition, it is not surprising that we find that the cysteinyl leukotrienes are implicated in both afferent and efferent cell-based immune responses, chronic inflammatory cell responses, and, as originally recognized, in acute smooth muscle constriction. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:182 / 187
页数:6
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