Selective loss of gastrointestinal mast cells and impaired immunity in PI3K-deficient mice

被引:174
作者
Fukao, T
Yamada, T
Tanabe, M
Terauchi, Y
Ota, T
Takayama, T
Asano, T
Takeuchi, T
Kadowaki, T
Hata, J
Koyasu, S
机构
[1] Keio Univ, Sch Med, Dept Microbiol & Immunol, Shinjuku Ku, Tokyo 1608582, Japan
[2] Keio Univ, Sch Med, Dept Pathol, Shinjuku Ku, Tokyo 1608582, Japan
[3] Keio Univ, Sch Med, Dept Trop Med & Parasitol, Shinjuku Ku, Tokyo 1608582, Japan
[4] Univ Tokyo, Grad Sch Med, Dept Metab Dis, Bunkyo Ku, Tokyo 1138655, Japan
关键词
D O I
10.1038/ni768
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mice that lack the p85alpha regulatory subunit of phosphatidylinositol-3 kinase (PI3K) are deficient in gastrointestinal and peritoneal mast cells but have dermal mast cells. Accordingly, these mice show impaired bacterial clearance in response to acute septic peritonitis and are highly susceptible to infection by the intestinal nematode Strongyloides venezuelensis. Systemic anaphylactic shock responses, however, are intact. We found that although reconstitution of PI3K(-/-) mice with bone marrow-derived mast cells (BMMCs) restored anti-bacterial immunity, only T helper type 2 (T(H)2)-conditioned BMMCs, not "standard" BMMCs, were able to restore anti-nematode immunity. This finding highlights the importance of the T(H)2 response in the control of nematode infection. Thus, PI3K likely plays an essential role in host immune responses by regulating both the development and induction of mast cells.
引用
收藏
页码:295 / 304
页数:10
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