Proliferating cell nuclear antigen in neutrophil fate

被引:19
|
作者
Witko-Sarsat, Veronique [1 ,2 ,3 ,4 ]
Ohayon, Delphine [1 ,2 ,3 ,4 ]
机构
[1] INSERM, U1016, Paris, France
[2] Univ Paris 05, Sorbonne Paris Cite, Fac Med, Inst Cochin, Paris, France
[3] CNRS, UMR 8104, Paris, France
[4] Labex Inflamex, Ctr Excellence, Paris, France
关键词
apoptosis; cell death; nuclear export; POLYMERASE PROCESSIVITY FACTOR; DNA-REPLICATION; PCNA-BINDING; CRYSTAL-STRUCTURE; POSTTRANSLATIONAL MODIFICATIONS; INFLAMMATION RESOLUTION; DIFFERENTIATION ANTIGEN; STAPHYLOCOCCUS-AUREUS; GENE-EXPRESSION; APOPTOSIS;
D O I
10.1111/imr.12449
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The life span of a neutrophil is a tightly regulated process as extended survival is beneficial for pathogen elimination and cell death necessary to prevent cytotoxic content release from activated neutrophils at the inflammatory site. Therefore, the control between survival and death must be a dynamic process. We have previously described that proliferating cell nuclear antigen (PCNA) which is known as a nuclear protein pivotal in DNA synthesis, is a key element in controlling neutrophil survival through its association with procaspases. Contrary to the dogma which asserted that PCNA has a strictly nuclear function, in mature neutrophils, PCNA is present exclusively within the cytosol due to its nuclear export at the end of the granulocytic differentiation. More recent studies are consistent with the notion that the cytosolic scaffold of PCNA is aimed at modulating neutrophil fate rather than simply preventing death. Ultimately, targeting neutrophil survival might have important applications not just in the field of immunology and inflammation, but also in hematology and transfusion. The neutrophil emerges as a unique and powerful cellular model to unravel the basic mechanisms governing the cell cycle-independent functions of PCNA and should be considered as a leader of the pack.
引用
收藏
页码:344 / 356
页数:13
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