Abstract

Since its discovery in Drosophila, the Notch signaling pathway has been studied in numerous developmental contexts in diverse multicellular organisms. The role of Notch signaling in nervous system development has been extensively investigated by numerous scientists, partially because many of the core Notch signaling components were initially identified through their dramatic ‘neurogenic’ phenotype of developing fruit fly embryos. Components of the Notch signaling pathway continue to be expressed in mature neurons and glia cells, which is suggestive of a role in the post-developmental nervous system. The Notch pathway has been, so far, implicated in learning and memory, social behavior, addiction, and other complex behaviors using genetic model organisms including Drosophila and mice. Additionally, Notch signaling has been shown to play a modulatory role in several neurodegenerative disease model animals and in mediating neural toxicity of several environmental factors. In this paper, we summarize the knowledge pertaining to the post-developmental roles of Notch signaling in the nervous system with a focus on discoveries made using the fruit fly as a model system as well as relevant studies in C elegans, mouse, rat, and cellular models. Since components of this pathway have been implicated in the pathogenesis of numerous psychiatric and neurodegenerative disorders in human, understanding the role of Notch signaling in the mature brain using model organisms will likely provide novel insights into the mechanisms underlying these diseases.

Highlights

  • Notch signaling is an evolutionarily conserved signaling pathway that has primarily been studied in the context of development and cancer [1,2,3]

  • Canonical Notch signaling is mediated by Notch receptors [NOTCH1-4 in human, Notch (N) in flies] that are activated by the Delta-family [DLL1, DLL3 and DLL4 in human, Delta (Dl) in flies] or Serrate/Jagged-family [JAG1 and JAG2 in human, Serrate (Ser) in flies] ligands presented by neighboring cells [4,5]

  • Another work identified that a candidate peptide drug (GM604) that has been developed for Amyotrophic Lateral Sclerosis (ALS) treatment can activate Notch signaling along with other pathways when tested in a human cell line [232], which indicates that activation of Notch signaling may have beneficial effects on neuronal survival

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Summary

Introduction

Notch signaling is an evolutionarily conserved signaling pathway that has primarily been studied in the context of development and cancer [1,2,3]. Exciting research related to the role of Notch signaling in adult neurogenesis as well as non-neuronal cells in the brain, including blood vascular and immune components, are actively being studied by many experts in the field, we will only briefly touch upon these topics and, instead, refer the readers to the following review articles that cover these topics in more detail [34,35,36,37] This is because there are very limited reports of adult neurogenesis in the mature fly brain [38], and vertebrates and invertebrates have some differences in the circulatory (e.g., flies have an open circulatory system and rely on their trachea for respiration) and immune (e.g., cells that have microglia-like function exist, flies lack adaptive immune cells) systems [39,40]. Post-Developmental Notch Signaling in Behavior and Neural Physiology (Table 1)

Notch Signaling in Learning and Memory
Notch Signaling in Reward and Addiction
Notch Signaling in Sleep Homeostasis
Post-Developmental Notch Signaling in Other Behaviors
Notch Signaling is Regulated by Neuronal Activity
Post-Developmental Notch Signaling Regulates Neural and Synaptic Physiology
Post-Developmental Notch Signaling Regulates Neuronal Morphology
Notch Signaling in Neuronal Maintenance
Prion Diseases
Neurotoxic Environmental Factors
Conclusions and Future Directions
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