Authors
Zhixun Dou, Kanad Ghosh, Maria Grazia Vizioli, Jiajun Zhu, Payel Sen, Kirk J Wangensteen, Johayra Simithy, Yemin Lan, Yanping Lin, Zhuo Zhou, Brian C Capell, Caiyue Xu, Mingang Xu, Julia E Kieckhaefer, Tianying Jiang, Michal Shoshkes-Carmel, KM Ahasan Al Tanim, Glen N Barber, John T Seykora, Sarah E Millar, Klaus H Kaestner, Benjamin A Garcia, Peter D Adams, Shelley L Berger
Publication date
2017/10/19
Journal
Nature
Volume
550
Issue
7676
Pages
402-406
Publisher
Nature Publishing Group UK
Description
Chromatin is traditionally viewed as a nuclear entity that regulates gene expression and silencing,,. However, we recently discovered the presence of cytoplasmic chromatin fragments that pinch off from intact nuclei of primary cells during senescence,, a form of terminal cell-cycle arrest associated with pro-inflammatory responses. The functional significance of chromatin in the cytoplasm is unclear. Here we show that cytoplasmic chromatin activates the innate immunity cytosolic DNA-sensing cGAS–STING (cyclic GMP–AMP synthase linked to stimulator of interferon genes) pathway, leading both to short-term inflammation to restrain activated oncogenes and to chronic inflammation that associates with tissue destruction and cancer. The cytoplasmic chromatin–cGAS–STING pathway promotes the senescence-associated secretory phenotype in primary human cells and in mice. Mice deficient in STING show impaired …
Total citations
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