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(Re)building the nervous system: A review of neuron–glia interactions from development to disease

  • Matthew D. Demmings
  • , Luana da Silva Chagas
  • , Marianela E. Traetta
  • , Rui S. Rodrigues
  • , Maria Florencia Acutain
  • , Evgeny Barykin
  • , Ashok Kumar Datusalia
  • , Liliana German-Castelan
  • , Vanesa S. Mattera
  • , Pedzisai Mazengenya
  • , Cecilia Skoug
  • , Hisashi Umemori
  • Western University
  • Universidade Federal Fluminense
  • Conicet
  • Neurocentre Magendie
  • Engelhardt Institute of Molecular Biology, Russian Academy of Sciences
  • National Institute of Pharmaceutical Education and Research, Raebareli
  • Universidad de Buenos Aires
  • University College London
  • Harvard University

Research output: Contribution to journalReview articlepeer-review

22 Scopus citations

Abstract

Neuron–glia interactions are fundamental to the development and function of the nervous system. During development, glia, including astrocytes, microglia, and oligodendrocytes, influence neuronal differentiation and migration, synapse formation and refinement, and myelination. In the mature brain, glia are crucial for maintaining neural homeostasis, modulating synaptic activity, and supporting metabolic functions. Neurons, inherently vulnerable to various stressors, rely on glia for protection and repair. However, glia, in their reactive state, can also promote neuronal damage, which contributes to neurodegenerative and neuropsychiatric diseases. Understanding the dual role of glia—as both protectors and potential aggressors—sheds light on their complex contributions to disease etiology and pathology. By appropriately modulating glial activity, it may be possible to mitigate neurodegeneration and restore neuronal function. In this review, which originated from the International Society for Neurochemistry (ISN) Advanced School in 2019 held in Montreal, Canada, we first describe the critical importance of glia in the development and maintenance of a healthy nervous system as well as their contributions to neuronal damage and neurological disorders. We then discuss potential strategies to modulate glial activity during disease to protect and promote a properly functioning nervous system. We propose that targeting glial cells presents a promising therapeutic avenue for rebuilding the nervous system. (Figure presented.)

Original languageEnglish
Article numbere16258
JournalJournal of Neurochemistry
Volume169
Issue number1
DOIs
StatePublished - Jan 2025

Keywords

  • astrocyte
  • brain development and function
  • glial dysfunction
  • microglia
  • neurodegenerative and neuropsychiatric disorders
  • oligodendrocyte

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