Active Brain & Nervous System Heart, Stroke & Blood

Understanding and harnessing the regenerative potential of the brain

In plain English

AI plain-English summary

A mouse pup’s brain can bounce back from injury at birth, but an adult mouse’s brain cannot—and scientists want to know why. This matters because the adult human brain also has very limited ability to repair itself after stroke, trauma, or disease. The researcher has already shown that newborn mice regenerate cerebellar tissue through a process called lineage plasticity, where cells change their identity to replace lost ones. Adult mice still harbour stem-like cells, but those cells no longer mount a regenerative response. By comparing the molecular signals active in neonatal versus adult mouse brains, the team aims to identify the specific signalling pathways and gene regulatory networks that enable regeneration in the young brain and are switched off in the old. If the research succeeds, it could reveal how to reactivate those dormant pathways in adult human stem cells. That would provide a basis for developing therapies that stimulate the brain to repair itself from within—without needing to transplant cells or build artificial tissue. This is fundamental science: it will uncover core regulatory mechanisms governing neural progenitors, and any future clinical application would depend on translating the findings from mouse models to humans. Similar fundamental work on developmental biology has previously opened paths to regenerative medicine.

View original technical description
Regeneration in the mature brain is limited. An understanding of the molecular mechanisms that regulate self-renewal, proliferation, differentiation, and importantly, the lineage plasticity of neural stem/progenitor cells during development and homeostasis is crucial for discovering how to stimulate brain repair upon injury. My previous work shows that the neonatal mouse cerebellum has remarkable regenerative potential as it can recover from injury at birth by various mechanisms, one of which involves lineage plasticity. However, the adult cerebellum has lost this regenerative ability, despite the existence of stem-like cells. Using comparative approaches in this powerful system, we will identify the signalling pathways and gene regulatory networks that control the developmental and regenerative responses of cerebellar progenitors in neonates and determine how they differ in adults. Candidate stimulators of neonatal regeneration will be tested through in vitro and in vivo stem cell assays, and then pro-regenerative pathways will be assessed for their ability to stimulate stem cells. Finally, we will develop models to translate our findings from mouse to human. This work will provide fundamental knowledge on the regulatory mechanisms that govern neural progenitors and harnessing new findings will provide a basis for in vivo manipulation of stem cells to facilitate brain repair.

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Researchers

Sumru Bayin (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Epigenetic mechanisms regulating pluripotency from embryonic to adult neurogeneisis
Molecular control of self-renewal and neurogenic characteristics of cortical progenitors
The Role of Neural Activity in Enhancing Axon and Presynaptic Regeneration in the Adult Injured Neocortex In Vivo
Modelling in vivo lineage reprogramming of human astrocytes into induced neurons in the adult mouse brain
Investigating cerebellar microglia diversity through development and injury

Original classification

Career Development Award

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