Impaired pulmonary host defense in mice lacking expression of the CXC chemokine Lungkine

被引:67
|
作者
Chen, SC
Mehrad, B
Deng, JC
Vassileva, G
Manfra, DJ
Cook, DN
Wiekowski, MT
Zlotnik, A
Standiford, TJ
Lira, SA
机构
[1] Schering Plough Corp, Res Inst, Dept Immunol, Kenilworth, NJ 07033 USA
[2] Univ Texas, SW Med Ctr, Div Pulm & Crit Care Med, Dallas, TX 75390 USA
[3] Univ Michigan, Sch Med, Dept Med, Div Pulm & Crit Care Med, Ann Arbor, MI 48109 USA
[4] DNAX Res Inst Mol & Cellular Biol Inc, Res Inst, Palo Alto, CA 94304 USA
来源
JOURNAL OF IMMUNOLOGY | 2001年 / 166卷 / 05期
关键词
D O I
10.4049/jimmunol.166.5.3362
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lungkine (CXCL15) is a novel CXC chemokine that is highly expressed in the adult mouse lung. To determine the biologic function of Lungkine, we generated Lungkine nub mice by targeted gene disruption. These mice did not differ from wild-type mice in their hematocrits or in the relative number of cells in leukocyte populations of peripheral blood or other tissues, including lung and bone marrow. However, Lungkine null mice were more susceptible to Klebsiella pneumonia infection, with a decreased survival and increased lung bacterial burden compared with infected wild-type mice. Histologic analysis of the lung and assessment of leukocytes in the bronchioalveolar lavage revealed that neutrophil numbers were normal in the lung parenchyma, but reduced in the airspace. The production of other neutrophil chemoattractants in the Lungkine null mice did not differ from that in wild-type mice, and neutrophil migration into other tissues was normal. Taken together, these findings demonstrate that Lungkine is an important mediator of neutrophil migration from the lung parenchyma into the airspace.
引用
收藏
页码:3362 / 3368
页数:7
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