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Microglial inflammation in genome instability: A neurodegenerative perspective.
Maliar, Nina L; Talbot, Emily J; Edwards, Abigail R; Khoronenkova, Svetlana V.
Afiliação
  • Maliar NL; Department of Biochemistry, University of Cambridge, Cambridge, UK.
  • Talbot EJ; Department of Biochemistry, University of Cambridge, Cambridge, UK.
  • Edwards AR; Cancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, Cambridge, UK.
  • Khoronenkova SV; Department of Biochemistry, University of Cambridge, Cambridge, UK. Electronic address: sk870@cam.ac.uk.
DNA Repair (Amst) ; 135: 103634, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38290197
ABSTRACT
The maintenance of genome stability is crucial for cell homeostasis and tissue integrity. Numerous human neuropathologies display chronic inflammation in the central nervous system, set against a backdrop of genome instability, implying a close interplay between the DNA damage and immune responses in the context of neurological disease. Dissecting the molecular mechanisms of this crosstalk is essential for holistic understanding of neuroinflammatory pathways in genome instability disorders. Non-neuronal cell types, specifically microglia, are major drivers of neuroinflammation in the central nervous system with neuro-protective and -toxic capabilities. Here, we discuss how persistent DNA damage affects microglial homeostasis, zooming in on the cytosolic DNA sensing cGAS-STING pathway and the downstream inflammatory response, which can drive neurotoxic outcomes in the context of genome instability.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microglia / Inflamação Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microglia / Inflamação Idioma: En Ano de publicação: 2024 Tipo de documento: Article