ROS generated by pollen NADPH oxidase provide a signal that augments antigen-induced allergic airway inflammation

被引:295
作者
Boldogh, I
Bacsi, A
Choudhury, BK
Dharajiya, N
Alam, R
Hazra, TK
Mitra, S
Goldblum, RM
Sur, S
机构
[1] Univ Texas, Med Branch, NIH Asthma & Allerg Dis Res Ctr, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Dept Microbiol & Immunol, Galveston, TX USA
[3] Univ Texas, Med Branch, Dept Internal Med, Galveston, TX 77550 USA
[4] Natl Jewish Med & Res Ctr, Dept Med, Div Allergy & Immunol, Denver, CO USA
[5] UTMB, Dept Pediat, Galveston, TX USA
关键词
D O I
10.1172/JCI24422
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Pollen exposure induces allergic airway inflammation in sensitized subjects. The role of antigenic pollen proteins in the induction of allergic airway inflammation is well characterized, but the contribution of other constituents in pollen grains to this process is unknown. Here we show that pollen grains and their extracts contain intrinsic NADPH oxidases. The pollen NADPH oxidases rapidly increased the levels of ROS in lung epithelium as well as the amount of oxidized glutathione (GSSG) and 4-hydroxynonenal (4-HNE) in airway-lining fluid. These oxidases, as well as products of oxidative stress (such as GSSG and 4-HNE) generated by these enzymes, induced neutrophil recruitment to the airways independent of the adaptive immune response. Removal of pollen NADPH oxidase activity from the challenge material reduced antigen-induced allergic airway inflammation, the number of mucin-containing cells in airway epithelium, and antigen-specific IgE levels in sensitized mice. Furthermore, challenge with Amb a 1, the major antigen in ragweed pollen extract that does not possess NADPH oxidase activity, induced low-grade allergic airway inflammation. Addition of GSSG or 4-HNE to Amb a I challenge material boosted allergic airway inflammation. We propose that oxidative stress generated by pollen NADPH oxidases (signal 1) augments allergic airway inflammation induced by pollen antigen (signal 2).
引用
收藏
页码:2169 / 2179
页数:11
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