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August 20, 2001The Journal of Experimental MedicineOpen Access

Requirement of Interleukin 17 Receptor Signaling for Lung Cxc Chemokine and Granulocyte Colony-Stimulating Factor Expression, Neutrophil Recruitment, and Host Defense

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Authors

PYPeng YeArmy Medical UniversityFRFred H. RodriguezAdult Congenital Heart DiseaseSKSuzanne T. KanalyUniversity of Iowa

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Implication

Murine study reveals critical role of interleukin 17 receptor signaling in pulmonary defense against bacteria, highlighting mechanisms predisposing CD4-deficient hosts to pneumonia.

Key Points

  • To determine whether interleukin-17 receptor signaling is required for granulocyte colony-stimulating factor production, CXC chemokine expression, and pulmonary host defense against bacterial infection.
  • Inoculated mice genetically deficient in interleukin-17 receptor (IL-17R KO) or overexpressing soluble IL-17R with intranasal Klebsiella pneumoniae.
  • Measured survival, bacterial dissemination, alveolar neutrophil recruitment, and lung expression of G-CSF and MIP-2 mRNA and protein.
  • IL-17R knockout mice experienced 100% mortality within 48 hours compared to 40% mortality in control mice.
  • IL-17R-deficient mice exhibited delayed neutrophil recruitment into alveolar spaces alongside increased systemic dissemination of K. pneumoniae.
  • Lungs of IL-17R knockout mice showed significant reductions in steady-state mRNA and protein levels of G-CSF and MIP-2 following bacterial challenge.

Cite This Study

Ye et al. (2001) studied this question.

synapsesocial.com/papers/69df80bd6324afb55d592bd8https://doi.org/10.1084/jem.194.4.519
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Also Consider

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