Publication:
TET2 Regulates the Neuroinflammatory Response in Microglia.

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2019

Authors

Carrillo-Jimenez, Alejandro
Deniz, Özgen
Niklison-Chirou, Maria Victoria
Ruiz, Rocio
Bezerra-Salomão, Karina
Stratoulias, Vassilis
Amouroux, Rachel
Yip, Ping Kei
Vilalta, Anna
Cheray, Mathilde

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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.

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MeSH Terms

Alzheimer Disease
Amyloid
Animals
Brain
DNA-Binding Proteins
Dioxygenases
Enhancer Elements, Genetic
Humans
Interleukin-6
Lipopolysaccharides
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
Microglia
Nitric Oxide Synthase Type II
Proto-Oncogene Proteins
RNA Interference
RNA, Small Interfering
Rats
Transcription Factor RelA
Transcription, Genetic

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Keywords

TET2, TLR-4, epigenetics, metabolism, microglia, neuroinflammation

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