Effects of estradiol in adult neurogenesis and brain repair in zebrafish
- Authors
- Diotel, N., Vaillant, C., Gabbero, C., Mironov, S., Fostier, A., Gueguen, M.M., Anglade, I., Kah, O., and Pellegrini, E.
- ID
- ZDB-PUB-120424-21
- Date
- 2013
- Source
- Hormones and behavior 63(2): 193-207 (Journal)
- Registered Authors
- Diotel, Nicolas, Kah, Olivier
- Keywords
- Aromatase B, brain repair, estrogen, lesion, neurogenesis, radial glial cells, zebrafish, teleost
- MeSH Terms
-
- Adult Stem Cells/drug effects*
- Adult Stem Cells/physiology
- Age Factors
- Animals
- Brain Injuries/physiopathology*
- Cell Proliferation/drug effects
- Disease Models, Animal
- Estradiol/pharmacology*
- Male
- Models, Biological
- Nerve Regeneration/drug effects
- Nerve Regeneration/physiology
- Neurogenesis/drug effects*
- Prosencephalon/drug effects
- Prosencephalon/physiology
- Wound Healing/drug effects*
- Wound Healing/physiology
- Zebrafish*
- PubMed
- 22521210 Full text @ Horm. Behav.
The brain of the adult teleost fish exhibits intense neurogenic activity and an outstanding capability for brain repair. Remarkably, the brain estrogen-synthesizing enzyme, aromatase, is strongly expressed, particularly in adult fishes, in radial glial cells, which act as progenitors. Using zebrafish, we tested the hypothesis that estrogens affect adult neurogenesis and brain regeneration by modulating the neurogenic activity of radial glial cells. To investigate this, the estrogenic environment was modified through inhibition of aromatase activity, blockade of nuclear estrogen receptors, or estrogenic treatments. Estrogens significantly decreased cell proliferation and migration at the olfactory bulbs/telencephalon junction and in the mediobasal hypothalamus. It also appears that cell survival is reduced at the olfactory bulbs/telencephalon junction. We also developed a model of telencephalic lesion to assess the role of aromatase and estrogens in brain repair. Proliferation increased rapidly immediately after the lesion in the parenchyma of the injured telencephalon, while proliferation at the ventricular surface appeared after 48 h and peaked at 7 days. At this time, most proliferative cells express Sox2, however, none of these Sox2 positive cells correspond to aromatase B-positive radial glial cells. Interestingly, aromatase B expression was significantly reduced 48 h and 7 days after the injury, but surprisingly, at 72 h after lesion, aromatase B expression appeared de novo expressed in parenchyma cells, suggesting a role for this ectopic expression of aromatase in brain repair mechanisms. Altogether these data suggest that estrogens modulate adult, but not reparative neurogenesis, in zebrafish. This article is part of a Special Issue entitled Hormones & Neurotrauma.