Completed Genetics & Molecular Biology Brain & Nervous System

Sexy glia: developmental plasticity during glia-derived neurogenesis

In plain English

AI plain-English summary

In the nervous system of a tiny roundworm, stable glial cells spontaneously transform into neurons during sexual maturation. This matters because it challenges a long-held biological assumption: that once a cell fully differentiates, its identity is fixed. The researchers have identified two such glia-to-neuron switches in *C. elegans*, a transparent worm whose entire cell lineage is mapped. This allows them to watch the process unfold at the single-cell level in a genetically tractable animal. They will combine classic genetics with next-generation sequencing to map the molecular and epigenetic changes driving this natural transdifferentiation, and to determine whether cell division is required. This is fundamental curiosity-driven science with no immediate practical application. However, glial cells in the human brain vastly outnumber neurons and are known to retain some neurogenic potential. Understanding how a worm’s glia naturally reprogram themselves could, in the long term, reveal molecular levers for coaxing human glia into replacing neurons lost to injury or disease—a therapeutic possibility the researchers explicitly note. Similar fundamental discoveries in cell plasticity have already reshaped regenerative medicine.

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The overall goal of this proposal is to elucidate the cellular and molecular mechanisms that regulate natural glia-to-neuron cell-fate switches. Stably differentiated cells can sometimes display a remarkable degree of plasticity and switch fates to another differentiated cell type, in a process termed transdifferentiation. In the vertebrate nervous system, radial glia act as neural progenitors during embryogenesis. Suprisingly, stably differentiated glia can also act as neural progenitors during adult neurogenesis. We have recently discovered two cases in which stably differentiated glial cells undergo a glia-to-neuron cell-fate switch during sexual maturation in the nervous system of C. elegans, allowing us to study these events at the single-cell level in a genetically tractable system. We will combine classic genetic approaches with state-of-the-art molecular and next-generation sequencing approaches to characterise the molecular and epigenetic changes that occur during natural glia-to-neuron transdifferentiation. We will elucidate the role of cell division in this process, identify novel molecular regulators and determine the reprogramming abilities of the factors we identify. Unleashing the neurogenic potential of glia offers tremendous therapeutic possibilities.

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Researchers

Richard Poole (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Deconstructing in vivo glia-to-neuron conversion
In vivo analysis of the proliferative properties and morphological dynamics of radial glial cells in the Xenopus brain
Cellular and molecular mechanisms of glial patterning and morphogenesis
Exploring glial roles in sculpting brain development
Molecular control of self-renewal and neurogenic characteristics of neural progenitors

Original classification

Senior Research Fellowship Basic

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