Interferon γ induction of pulmonary emphysema in the adult murine lung

被引:311
作者
Wang, ZD
Zheng, T
Zhu, Z
Homer, RJ
Riese, RJ
Chapman, HA
Shapiro, SD
Elias, JA
机构
[1] Yale Univ, Sch Med, Dept Internal Med, Pulm & Crit Care Med Sect, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
[3] VA Connecticut Hlth Care Syst, Pathol & Lab Med Serv, West Haven, CT 06516 USA
[4] Harvard Univ, Boston, MA 02115 USA
[5] Univ Calif San Francisco, Sch Med, Inst Cardiovasc Res, San Francisco, CA 94163 USA
[6] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
关键词
chronic obstructive pulmonary disease; matrix metalloproteinase; cathepsin; neutrophil; secretory leukocyte proteinase inhibitor;
D O I
10.1084/jem.192.11.1587
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chronic inflammation containing CD8(+) lymphocytes, neutrophils, and macrophages, and pulmonary emphysema coexist in lungs from patients with chronic obstructive pulmonary disease. Although this inflammatory response is believed to cause the remodeling that is seen in these tissues, the mechanism(s) by which inflammation causes emphysema have not been defined. Here we demonstrate that interferon gamma (IFN-gamma), a prominent product of CD8(+) cells, causes emphysema with alveolar enlargement, enhanced lung volumes, enhanced pulmonary compliance, and macrophage- and neutrophil-rich inflammation when inducibly targeted, in a transgenic fashion, to the adult murine lung. Prominent protease and antiprotease alterations were also noted in these mice. They included the induction and activation of matrix metalloproteinase (MMP)-12 and cathepsins B, H, D, S, and L, the elaboration of MMP-9, and the selective inhibition of secretory leukocyte proteinase inhibitor. IFN-gamma causes emphysema and alterations in pulmonary protease/antiprotease balance when expressed in pulmonary tissues.
引用
收藏
页码:1587 / 1599
页数:13
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