Caveolin-1 Modifies the Immunity to Pseudomonas aeruginosa

被引:42
作者
Gadjeva, Mihaela [1 ]
Paradis-Bleau, Catherine [1 ]
Priebe, Gregory P. [1 ,3 ]
Fichorova, Raina [2 ]
Pier, Gerald B. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med,Channing Lab, Boston, MA 02115 USA
[2] Harvard Univ, Brigham & Womens Hosp, Lab Genital Tract Biol, Dept Obstet Gynecol & Reprod Biol,Sch Med, Boston, MA 02115 USA
[3] Childrens Hosp Boston, Dept Anesthesiol, Boston, MA 02115 USA
关键词
TRANSMEMBRANE CONDUCTANCE REGULATOR; III PROTEIN SECRETION; CYSTIC-FIBROSIS MICE; EPITHELIAL-CELLS; LUNG INFECTION; LIPID RAFTS; MEMBRANE DOMAINS; EXPRESSION; MACROPHAGES; RESISTANCE;
D O I
10.4049/jimmunol.0900604
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The inflammatory response to Pseudomonas aeruginosa is not properly regulated in the lungs of patients with cystic fibrosis (CF). In the lung epithelium of individuals with wild-type CIF transmembrane conductance regulator, lipid rafts containing CF trans-membrane conductance regulator are rapidly formed in response to P. aeruginosa infection, and this response is closely linked to resistance to infection and disease. We found these rafts also contained high levels of caveolin-1 and thus examined the sensitivity of cav1 knockout (KO) mice to P. aeruginosa challenge in both acute and chronic P. aeruginosa infection models. We found that cav1 KO mice had increased sensitivity to P. aeruginosa infection, as represented by an increased mortality rate, elevated bacterial burdens recovered from lungs and spleens, and elevated inflammatory responses. These findings correlated with the decreased ability of cav1-deficient neutrophils to phagocytose P. aeruginosa. In addition, P. aeruginosa colonized cav1 KO mice much better compared with the wild-type controls in a model of chronic infection, indicting an important contribution of Cav-1 to innate host immunity to P. aeruginosa infection in the setting of both acute pneumonia and chronic infection typical of CF. The Journal of Immunology, 2010, 184: 296-302.
引用
收藏
页码:296 / 302
页数:7
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