Host Cell Polarity Proteins Participate in Innate Immunity to Pseudomonas aeruginosa Infection

Autor: Travis R. Ruch, David M. Bryant, Arlinet Kierbel, Ross J. Metzger, Anirban Datta, Keith E. Mostov, Torsten Wittmann, Cindy S. Tran, Joanne N. Engel, Yoni Eran, Paul Brakeman
Jazyk: angličtina
Rok vydání: 2014
Předmět:
rac1 GTP-Binding Protein
Cancer Research
Cystic Fibrosis
Phosphatidylinositol 3-Kinases
Innate
2.2 Factors relating to the physical environment
polarity
Aetiology
Lung
Epithelial polarity
NF-kappa B
Cell Polarity
Cell biology
Infectious Diseases
medicine.anatomical_structure
Medical Microbiology
Pseudomonas aeruginosa
Pneumonia & Influenza
Infection
CIENCIAS NATURALES Y EXACTAS
Otras Ciencias Biológicas
Immunology
Nerve Tissue Proteins
RAC1
Flagellum
Biology
Microbiology
Article
Cell Line
Vaccine Related
Ciencias Biológicas
Rare Diseases
Immune system
Biodefense
Immunology and Microbiology(all)
Virology
medicine
Humans
Pseudomonas Infections
Secretion
Molecular Biology
Polarity (international relations)
Innate immune system
Prevention
Immunity
epithelia
Epithelial Cells
Pneumonia
Immunity
Innate

Epithelium
Emerging Infectious Diseases
Parasitology
native immunity
Carrier Proteins
Zdroj: Cell host & microbe, vol 15, iss 5
Popis: The mucosal epithelium consists of polarized cells with distinct apical and basolateral membranes that serve as functional and physical barriers to external pathogens. The apical surface of the epithelium constitutes the first point of contact between mucosal pathogens, such as Pseudomonas aeruginosa, and their host. We observed that binding of P. aeruginosa aggregates to the apical surface of polarized cells led to the striking formation of an actin-rich membrane protrusion with inverted polarity, containing basolateral lipids and membrane components. Such protrusions were associated with a spatially localized host immune response to P. aeruginosa aggregates that required bacterial flagella and a type III secretion system apparatus. Host protrusions formed de novo underneath bacterial aggregates and involved the apical recruitment of a Par3/Par6α/aPKC/Rac1 signaling module for a robust, spatially localized host NF-κB response. Our data reveal a role for spatiotemporal epithelial polarity changes in the activation of innate immune responses. Fil: Tran, Cindy S.. University of California; Estados Unidos Fil: Eran, Yonatan. University of California; Estados Unidos Fil: Ruch, Travis. University of California; Estados Unidos Fil: Bryant, David. University of California; Estados Unidos Fil: Datta, Aniriban. University of California; Estados Unidos Fil: Brakeman, Paul. University of California; Estados Unidos Fil: Kierbel, Arlinet Verónica. Instituto Pasteur de Montevideo; Uruguay. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Instituto de Investigaciones Biotecnológicas ; Argentina Fil: Wittman, Torsten. University of California; Estados Unidos Fil: Metzger, Ross. University of California; Estados Unidos Fil: Mostov, Keith. University of California; Estados Unidos Fil: Engel, Joanne. University of California; Estados Unidos
Databáze: OpenAIRE