Defining a link with asthma in mice congenitally deficient in eosinophils

被引:543
作者
Lee, JJ [1 ]
Dimina, D
Macias, MP
Ochkur, SI
McGarry, MP
O'Neill, KR
Protheroe, C
Pero, R
Nguyen, T
Cormier, SA
Lenkiewicz, E
Colbert, D
Rinaldi, L
Ackerman, SJ
Irvin, CG
Lee, NA
机构
[1] Mayo Clin Arizona, Div Pulm Med, Scottsdale, AZ 85259 USA
[2] Mayo Clin Arizona, Dept Biochem & Mol Biol, Scottsdale, AZ 85259 USA
[3] Mayo Clin Arizona, Div Hematol Oncol, Scottsdale, AZ 85259 USA
[4] Univ Vermont, Dept Med, Vermont Lung Ctr, Burlington, VT 05405 USA
[5] Univ Illinois, Coll Med, Dept Biochem & Mol Biol, Chicago, IL 60612 USA
关键词
D O I
10.1126/science.1099472
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Eosinophils are often dominant inflammatory cells present in the lungs of asthma patients. Nonetheless, the role of these leukocytes remains poorly understood. We have created a transgenic line of mice (PHIL) that are specifically devoid of eosinophils, but otherwise have a full complement of hematopoietically derived cells. Allergen challenge of PHIL mice demonstrated that eosinophils were required for pulmonary mucus accumulation and the airway hyperresponsiveness associated with asthma. The development of an eosinophil-less mouse now permits an unambiguous assessment of a number of human diseases that have been linked to this granulocyte, including allergic diseases, parasite infections, and tumorigenesis.
引用
收藏
页码:1773 / 1776
页数:4
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