Epidermal Growth Factor and Fibroblast Growth Factor-2 Have Different Effects on Neural Progenitors in the Adult Rat Brain
Autor: | Fred H. Gage, Jürgen Winkler, Gerd Kempermann, Leon J. Thal, H. G. Kuhn |
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Rok vydání: | 1997 |
Předmět: |
Male
medicine.medical_treatment Subventricular zone Cell Count Biology Epidermal growth factor Neurosphere medicine Animals Neurons Epidermal Growth Factor Stem Cells General Neuroscience Growth factor Neurogenesis Brain Articles Rats Inbred F344 Rats Olfactory bulb medicine.anatomical_structure Neuropoiesis nervous system Fibroblast Growth Factor 2 Olfactory ensheathing glia Neuroscience |
Zdroj: | The Journal of Neuroscience. 17:5820-5829 |
ISSN: | 1529-2401 0270-6474 |
DOI: | 10.1523/jneurosci.17-15-05820.1997 |
Popis: | Neurons and glia are generated throughout adulthood from proliferating cells in two regions of the rat brain, the subventricular zone (SVZ) and the hippocampus. This study shows that exogenous basic fibroblast growth factor (FGF-2) and epidermal growth factor (EGF) have differential and site-specific effects on progenitor cellsin vivo. Both growth factors expanded the SVZ progenitor population after 2 weeks of intracerebroventricular administration, but only FGF-2 induced an increase in the number of newborn cells, most prominently neurons, in the olfactory bulb, the normal destination for neuronal progenitors migrating from the SVZ. EGF, on the other hand, reduced the total number of newborn neurons reaching the olfactory bulb and substantially enhanced the generation of astrocytes in the olfactory bulb. Moreover, EGF increased the number of newborn cells in the striatum either by migration of SVZ cells or by stimulation of local progenitor cells. No evidence of neuronal differentiation of newborn striatal cells was found by three-dimensional confocal analysis, although many of these newborn cells were associated closely with striatal neurons. The proliferation of hippocampal progenitors was not affected by either growth factor. However, EGF increased the number of newborn glia and reduced the number of newborn neurons, similar to the effects seen in the olfactory bulb. These findings may be useful for elucidating thein vivorole of growth factors in neurogenesis in the adult CNS and may aid development of neuronal replacement strategies after brain damage. |
Databáze: | OpenAIRE |
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