| Literature DB >> 31618637 |
Alejandro Carrillo-Jimenez1, Özgen Deniz2, Maria Victoria Niklison-Chirou2, Rocio Ruiz1, Karina Bezerra-Salomão2, Vassilis Stratoulias3, Rachel Amouroux4, Ping Kei Yip2, Anna Vilalta5, Mathilde Cheray3, Alexander Michael Scott-Egerton2, Eloy Rivas6, Khadija Tayara1, Irene García-Domínguez1, Juan Garcia-Revilla1, Juan Carlos Fernandez-Martin1, Ana Maria Espinosa-Oliva1, Xianli Shen3, Peter St George-Hyslop7, Guy Charles Brown5, Petra Hajkova4, Bertrand Joseph3, Jose Luis Venero1, Miguel Ramos Branco8, Miguel Angel Burguillos9.
Abstract
Epigenomic mechanisms regulate distinct aspects of the inflammatory response in immune cells. Despite the central role for microglia in neuroinflammation and neurodegeneration, little is known about their epigenomic regulation of the inflammatory response. Here, we show that Ten-eleven translocation 2 (TET2) methylcytosine dioxygenase expression is increased in microglia upon stimulation with various inflammogens through a NF-κB-dependent pathway. We found that TET2 regulates early gene transcriptional changes, leading to early metabolic alterations, as well as a later inflammatory response independently of its enzymatic activity. We further show that TET2 regulates the proinflammatory response in microglia of mice intraperitoneally injected with LPS. We observed that microglia associated with amyloid β plaques expressed TET2 in brain tissue from individuals with Alzheimer's disease (AD) and in 5xFAD mice. Collectively, our findings show that TET2 plays an important role in the microglial inflammatory response and suggest TET2 as a potential target to combat neurodegenerative brain disorders.Entities:
Keywords: TET2; TLR-4; epigenetics; metabolism; microglia; neuroinflammation
Year: 2019 PMID: 31618637 DOI: 10.1016/j.celrep.2019.09.013
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423