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Unique aspects of IFN-γ/STAT1 signaling in neurons.
Clark, Danielle N; Begg, Lauren R; Filiano, Anthony J.
Afiliação
  • Clark DN; Department of Immunology, Duke University, Durham, North Carolina, USA.
  • Begg LR; Marcus Center for Cellular Cures, Duke University, Durham, North Carolina, USA.
  • Filiano AJ; Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Immunol Rev ; 311(1): 187-204, 2022 10.
Article em En | MEDLINE | ID: mdl-35656941
The IFN-γ/STAT1 immune signaling pathway impacts many homeostatic and pathological aspects of neurons, beyond its canonical role in controlling intracellular pathogens. Well known for its potent pro-inflammatory and anti-viral functions in the periphery, the IFN-γ/STAT1 pathway is rapidly activated then deactivated to prevent excessive inflammation; however, neurons utilize unique IFN-γ/STAT1 activation patterns, which may contribute to the non-canonical neuron-specific downstream effects. Though it is now well-established that the immune system interacts and supports the CNS in health and disease, many aspects regarding IFN-γ production in the CNS and how neurons respond to IFN-γ are unclear. Additionally, it is not well understood how the diversity of the IFN-γ/STAT1 pathway is regulated in neurons to control homeostatic functions, support immune surveillance, and prevent pathologies. In this review, we discuss the neuron-specific mechanisms and kinetics of IFN-γ/STAT1 activation, the potential sources and entry sites of IFN-γ in the CNS, and the diverse set of homeostatic and pathological effects IFN-γ/STAT1 signaling in neurons has on CNS health and disease. We will also highlight the different contexts and conditions under which IFN-γ-induced STAT1 activation has been studied in neurons, and how various factors might contribute to the vast array of downstream effects observed.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Transdução de Sinais / Neurônios Limite: Humans Idioma: En Revista: Immunol Rev Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Transdução de Sinais / Neurônios Limite: Humans Idioma: En Revista: Immunol Rev Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos