Author/Authors :
Juan C. Acosta، نويسنده , , Ana OʹLoghlen، نويسنده , , Ana Banito، نويسنده , , Maria V. Guijarro، نويسنده , , Arnaud Augert، نويسنده , , Selina Raguz، نويسنده , , Marzia Fumagalli، نويسنده , , Marco Da Costa، نويسنده , , Celia Brown، نويسنده , , Nikolay Popov، نويسنده , , Yoshihiro Takatsu، نويسنده , , Jonathan Melamed، نويسنده , , Fabrizio dʹAdda di Fagagna، نويسنده , , David Bernard، نويسنده , , Eva Hernando، نويسنده , , Jes?s Gil، نويسنده ,
Abstract :
Cells enter senescence, a state of stable proliferative arrest, in response to a variety of cellular stresses, including telomere erosion, DNA damage, and oncogenic signaling, which acts as a barrier against malignant transformation in vivo. To identify genes controlling senescence, we conducted an unbiased screen for small hairpin RNAs that extend the life span of primary human fibroblasts. Here, we report that knocking down the chemokine receptor CXCR2 (IL8RB) alleviates both replicative and oncogene-induced senescence (OIS) and diminishes the DNA-damage response. Conversely, ectopic expression of CXCR2 results in premature senescence via a p53-dependent mechanism. Cells undergoing OIS secrete multiple CXCR2-binding chemokines in a program that is regulated by the NF-κB and C/EBPβ transcription factors and coordinately induce CXCR2 expression. CXCR2 upregulation is also observed in preneoplastic lesions in vivo. These results suggest that senescent cells activate a self-amplifying secretory network in which CXCR2-binding chemokines reinforce growth arrest.
