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

被引:23
作者
Garrison, Sean P. [1 ]
Thornton, Justin A. [2 ]
Haecker, Hans [2 ]
Webby, Richard [2 ]
Rehg, Jerold E. [3 ]
Parganas, Evan [1 ]
Zambetti, Gerard P. [1 ]
Tuomanen, Elaine I. [2 ]
机构
[1] St Jude Childrens Hosp, Dept Biochem, Memphis, TN 38105 USA
[2] St Jude Childrens Hosp, Dept Infect Dis, Memphis, TN 38105 USA
[3] St Jude Childrens Hosp, Dept Pathol, Memphis, TN 38105 USA
关键词
PROGRAMMED CELL-DEATH; STREPTOCOCCUS-PNEUMONIAE; NEURONAL APOPTOSIS; BH3-ONLY PROTEINS; HYDROGEN-PEROXIDE; P53; MACROPHAGES; SURVIVAL; PATHOGENESIS; ACTIVATION;
D O I
10.1371/journal.ppat.1001240
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页数:11
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