Mice lacking the multidrug resistance protein 1 are resistant to Streptococcus pneumoniae-induced pneumonia
Mice lacking the multidrug resistance protein 1 are resistant to Streptococcus pneumoniae-induced pneumonia
复制标题
DOI：
10.4049/jimmunol.166.6.4059
复制
发表时间：
2001-03-15
影响因子：
4.4
通讯作者：
van der Poll, T
中科院分区：
文献类型：
--
作者：
Schultz, MJ;Wijnholds, J;van der Poll, T
Leukotrienes (LTs) are considered important for antibacterial defense in the lung. Multidrug resistance protein 1 (mrp1) is a transmembrane protein responsible for the cellular extrusion of LTC4. To determine the role of mrp1 in host defense against pneumonia, mrp1(-/-) and wild-type mice were intranasally inoculated with Streptococcus pneumoniae. mrp1(-/-) mice displayed a diminished outgrowth of pneumococci in lungs and a strongly reduced mortality. These findings were related to an effect of mrp1 on LT metabolism, because survival was similar in mrp1(-/-) and wild-type mice treated with the 5-lipoxygenase-activating protein inhibitor MK-886. Although LTC4 levels remained low in the bronchoalveolar lavage fluid of mrp1(-/-) mice, LTB4 concentrations were higher than in wild-type mice. These elevated LTB4 concentrations were important for the relative protection of mrp1(-/-) mice, because the LTB4 antagonist LTB4-dimethyl amide abolished their survival advantage. In vitro experiments suggested that the intracellullar accumulation of LTC4 in mrp1(-/-) mice results in product inhibition of LTC4-synthase, diminishing substrate competition between LTA(4)-hydrolase (which yields LTB4) and LTC4-synthase for the available LTA(4). We conclude that mrp1(-/-) mice are resistant against pneumococcal pneumonia by a mechanism that involves increased release of LTB4, These results identify mrp1 as a novel target for adjunctive therapy in pneumonia.
