4.6 Review

Cellular Mechanisms Participating in Brain Repair of Adult Zebrafish and Mammals after Injury

Journal

CELLS
Volume 10, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/cells10020391

Keywords

adult neurogenesis; brain injury; neural stem cell; regeneration; stroke; zebrafish; mice

Categories

Funding

  1. FEDER [RE0022527]
  2. EU-Region Reunion-French State national counterpart
  3. Helmholtz Association BioInterfaces in Technology and Medicine Program
  4. Deutsche Forschungsgemeinschaft training group [GRK2039]

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Adult neurogenesis is a conserved process in all vertebrates, but differences exist in the number of neurogenic niches, NSC identity, and regenerative capacity between zebrafish and mammals. Zebrafish has a higher number of neurogenic niches and displays strong regenerative capacity without scar formation, unlike mammals. Shared early events after brain injury include cell death, microglia recruitment, oligodendrocyte recruitment, and injury-induced neurogenesis, but mammals form a persistent glial scar whereas zebrafish do not, contributing to their higher regenerative capacity.
Adult neurogenesis is an evolutionary conserved process occurring in all vertebrates. However, striking differences are observed between the taxa, considering the number of neurogenic niches, the neural stem cell (NSC) identity, and brain plasticity under constitutive and injury-induced conditions. Zebrafish has become a popular model for the investigation of the molecular and cellular mechanisms involved in adult neurogenesis. Compared to mammals, the adult zebrafish displays a high number of neurogenic niches distributed throughout the brain. Furthermore, it exhibits a strong regenerative capacity without scar formation or any obvious disabilities. In this review, we will first discuss the similarities and differences regarding (i) the distribution of neurogenic niches in the brain of adult zebrafish and mammals (mainly mouse) and (ii) the nature of the neural stem cells within the main telencephalic niches. In the second part, we will describe the cascade of cellular events occurring after telencephalic injury in zebrafish and mouse. Our study clearly shows that most early events happening right after the brain injury are shared between zebrafish and mouse including cell death, microglia, and oligodendrocyte recruitment, as well as injury-induced neurogenesis. In mammals, one of the consequences following an injury is the formation of a glial scar that is persistent. This is not the case in zebrafish, which may be one of the main reasons that zebrafish display a higher regenerative capacity.

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