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The Journal of Neuroscience, March 15, 2003, 23(6):2239
Glutamate Promotes Proliferation of Striatal Neuronal Progenitors
by an NMDA Receptor-Mediated Mechanism
Kelvin C.
Luk1,
Timothy
E.
Kennedy2, and
Abbas F.
Sadikot1
1 Cone Laboratory and 2 Center for Neuronal
Survival, Department of Neurology and Neurosurgery, Montreal
Neurological Institute, McGill University, Montreal, H3A 2B4 Canada
Increasing evidence suggests that classical neurotransmitters play
important roles in the development of the mammalian CNS. We used
in vivo and in vitro models to identify a
novel role for glutamate in striatal neurogenesis mediated by
NMDA receptors. In utero exposure to NMDA
receptor antagonists during striatal neurogenesis caused a dramatic
reduction in the total number of adult striatal neurons. In contrast,
embryos exposed to NMDA receptor antagonists immediately after the main
period of neurogenesis showed no significant change in neuronal number
in the adult striatum. In addition, examination of embryos shortly
after NMDA receptor blockade revealed reduced proliferation in the
lateral ganglionic eminence (LGE). In culture, dividing neuronal
progenitors derived from the embryonic LGE showed marked reduction in
5'-bromodeoxyuridine (BrdU) uptake when exposed to NMDA receptor
antagonists, indicating reduced DNA synthesis. Low concentrations of
NMDA significantly increased proliferation, whereas high concentrations
were toxic. AMPA-KA receptor antagonists had no significant
effect on striatal neuroblast proliferation either in
vivo or in vitro. These results support the
hypothesis that glutamate plays a novel role during early development
of the ventral telencephalon, promoting proliferation of striatal
neuronal progenitors by an NMDA receptor-dependent mechanism. In
contrast, previous findings suggest that proliferation of cortical
progenitors derived from the dorsal telencephalon is regulated by
activation of AMPA-KA but not NMDA receptors. Heterogeneous
responses to glutamate in different germinal zones of the telencephalon
may be an important mechanism contributing to generating neuronal
diversity in the forebrain.
Key words:
forebrain; striatum; neurogenesis; neurotransmitter; BrdU; stereology
Copyright © 2003 Society for Neuroscience 0270-6474/03/2362239-12$05.00/0
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