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Formylpeptide receptors are critical for rapid neutrophil mobilization in host defense against Listeria monocytogenes.


ABSTRACT: Listeria monocytogenes (Listeria) causes opportunistic infection in immunocompromised hosts with high mortality. Resistance to Listeria depends on immune responses and recruitment of neutrophils of the immune system into infected sites is an early and critical step. Mouse neutrophils express two G protein-coupled formylpeptide receptor subtypes Fpr1 and Fpr2 that recognize bacterial and host-derived chemotactic molecules including Listeria peptides for cell migration and activation. Here we report deficiency in Fprs exacerbated the severity of the infection and increased the mortality of infected mice. The mechanism involved impaired early neutrophil recruitment to the liver with Fpr1 and Fpr2 being sole receptors for neutrophils to sense Listeria chemoattractant signals and for production of bactericidal superoxide. Thus, Fprs are essential sentinels to guide the first wave of neutrophil infiltration in the liver of Listeria-infected mice for effective elimination of the invading pathogen.

SUBMITTER: Liu M 

PROVIDER: S-EPMC3493074 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature

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Formylpeptide receptors are critical for rapid neutrophil mobilization in host defense against Listeria monocytogenes.

Liu Mingyong M   Chen Keqiang K   Yoshimura Teizo T   Liu Ying Y   Gong Wanghua W   Wang Aimin A   Gao Ji-Liang JL   Murphy Philip M PM   Wang Ji Ming JM  

Scientific reports 20121108


Listeria monocytogenes (Listeria) causes opportunistic infection in immunocompromised hosts with high mortality. Resistance to Listeria depends on immune responses and recruitment of neutrophils of the immune system into infected sites is an early and critical step. Mouse neutrophils express two G protein-coupled formylpeptide receptor subtypes Fpr1 and Fpr2 that recognize bacterial and host-derived chemotactic molecules including Listeria peptides for cell migration and activation. Here we repo  ...[more]

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