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The p53-Target Gene Puma Drives Neutrophil-Mediated Protection against Lethal Bacterial Sepsis

Disruption of p53/Puma-mediated apoptosis protects against lethality due to DNA damage. Here we demonstrate the unexpected requirement of the pro-apoptotic p53-target gene Puma to mount a successful innate immune response to bacterial sepsis. Puma(−/−) mice rapidly died when challenged with bacteria...

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Detalles Bibliográficos
Autores principales: Garrison, Sean P., Thornton, Justin A., Häcker, Hans, Webby, Richard, Rehg, Jerold E., Parganas, Evan, Zambetti, Gerard P., Tuomanen, Elaine I.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009602/
https://www.ncbi.nlm.nih.gov/pubmed/21203486
http://dx.doi.org/10.1371/journal.ppat.1001240
Descripción
Sumario:Disruption of p53/Puma-mediated apoptosis protects against lethality due to DNA damage. Here we demonstrate the unexpected requirement of the pro-apoptotic p53-target gene Puma to mount a successful innate immune response to bacterial sepsis. Puma(−/−) mice rapidly died when challenged with bacteria. While the immune response in Puma(−/−) mice was unchanged in cell migration, phagocytosis and bacterial killing, sites of infection accumulated large abscesses and sepsis was progressive. Blocking p53/Puma-induced apoptosis during infection caused resistance to ROS-induced cell death in the CD49d+ neutrophil subpopulation, resulting in insufficient immune resolution. This study identifies a biological role for p53/Puma apoptosis in optimizing neutrophil lifespan so as to ensure the proper clearance of bacteria and exposes a counter-balance between the innate immune response to infection and survival from DNA damage.