4.7 Article

Neuronal activity and Wnt signaling act through Gsk3-β to regulate axonal integrity in mature Drosophila olfactory sensory neurons

Journal

DEVELOPMENT
Volume 136, Issue 8, Pages 1273-1282

Publisher

COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.031377

Keywords

Drosophila; Olfactory system; Neuronal activity; Gsk-3 beta (Shaggy); Wingless

Funding

  1. NIDA NIH HHS [DA15495] Funding Source: Medline

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The roles played by signaling pathways and neural activity during the development of circuits have been studied in several different contexts. However, the mechanisms involved in maintaining neuronal integrity once circuits are established are less well understood, despite their potential relevance to neurodegeneration. We demonstrate that maintenance of adult Drosophila olfactory sensory neurons requires cell-autonomous neuronal activity. When activity is silenced, development occurs normally, but neurons degenerate in adulthood. These detrimental effects can be compensated by downregulating Glycogen synthase kinase-3 beta (Gsk-3 beta). Conversely, ectopic expression of activated Gsk-3 beta or downregulation of Wnt effectors also affect neuron stability, demonstrating a role for Wnt signaling in neuroprotection. This is supported by our observation that activated adult neurons are capable of increased Wingless release, and its targeted expression can protect neurons against degeneration. The role of Wnt signaling in this process is non-transcriptional, and may act on cellular mechanisms that regulate axonal or synaptic stability. Together, we provide evidence that Gsk-3 beta is a key sensor involved in neural circuit integrity, maintaining axon stability through neural activity and the Wnt pathway.

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