TY - JOUR
T1 - Aryl hydrocarbon receptor protects against bacterial infection by promoting macrophage survival and reactive oxygen species production
AU - Kimura, Akihiro
AU - Abe, Hiromi
AU - Tsuruta, Sanae
AU - Chiba, Sayuri
AU - Fujii-Kuriyama, Yoshiaki
AU - Sekiya, Takashi
AU - Morita, Rimpei
AU - Yoshimura, Akihiko
N1 - Funding Information:
Grant-in-Aid for Young Scientists (B) from the Ministry of Education, Culture, Sports, Science and Technology (23790545); the Mochida Memorial Foundation for Medical and Pharmaceutical research; Kanae Foundation for the Promotion of Medical Science; Mitsubishi Pharma Research Foundation; the Institute for Fermentation, Osaka.
PY - 2014/4
Y1 - 2014/4
N2 - Aryl hydrocarbon receptor (AhR) is crucial for various immune responses. The relationship between AhR and infection with the intracellular bacteria Listeria monocytogenes (LM) is poorly understood. Here, we show that in response to LM infection, AhR is required for bacterial clearance by promoting macrophage survival and reactive oxygen species (ROS) production. AhR-deficient mice were more susceptible to listeriosis, and AhR deficiency enhances bacterial growth in vivo and in vitro. On the other hand, pro-inflammatory cytokines were increased in AhR-deficient macrophages infected with LM despite enhanced susceptibility to LM infection in AhR-deficient mice. Subsequent studies demonstrate that AhR protects against macrophage cell death induced by LM infection through the induction of the antiapoptotic factor, the apoptosis inhibitor of macrophages, which promotes macrophage survival in the setting of LM infection. Furthermore, AhR promotes ROS production for bacterial clearance. Our results demonstrate that AhR is essential to the resistance against LM infection as it promotes macrophage survival and ROS production. This suggests that the activation of AhR by its ligands may be an effective strategy against listeriosis.
AB - Aryl hydrocarbon receptor (AhR) is crucial for various immune responses. The relationship between AhR and infection with the intracellular bacteria Listeria monocytogenes (LM) is poorly understood. Here, we show that in response to LM infection, AhR is required for bacterial clearance by promoting macrophage survival and reactive oxygen species (ROS) production. AhR-deficient mice were more susceptible to listeriosis, and AhR deficiency enhances bacterial growth in vivo and in vitro. On the other hand, pro-inflammatory cytokines were increased in AhR-deficient macrophages infected with LM despite enhanced susceptibility to LM infection in AhR-deficient mice. Subsequent studies demonstrate that AhR protects against macrophage cell death induced by LM infection through the induction of the antiapoptotic factor, the apoptosis inhibitor of macrophages, which promotes macrophage survival in the setting of LM infection. Furthermore, AhR promotes ROS production for bacterial clearance. Our results demonstrate that AhR is essential to the resistance against LM infection as it promotes macrophage survival and ROS production. This suggests that the activation of AhR by its ligands may be an effective strategy against listeriosis.
KW - Apoptosis inhibitor of macrophages
KW - Dioxin receptor
KW - Innate immunity
KW - Listeria monocytogenes
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U2 - 10.1093/intimm/dxt067
DO - 10.1093/intimm/dxt067
M3 - Article
C2 - 24343818
AN - SCOPUS:84897515710
SN - 0953-8178
VL - 26
SP - 209
EP - 220
JO - International immunology
JF - International immunology
IS - 4
M1 - dxt067
ER -