Adenovirally expressed noggin and brain-derived neurotrophic factor cooperate to induce new medium spiny neurons from resident progenitor cells in the adult striatal ventricular zone

被引:141
作者
Chmielnicki, E
Benraiss, A
Economides, AN
Goldman, SA
机构
[1] Univ Rochester, Dept Neurol, Rochester, NY 14642 USA
[2] Cornell Univ, Coll Med, Dept Neurol & Neurosci, New York, NY 10021 USA
[3] Regeneron Pharmaceut Inc, Tarrytown, NY 10591 USA
关键词
Huntington's disease; neurogenesis; subependymal zone; stem cells; gene therapy; regeneration;
D O I
10.1523/JNEUROSCI.1554-03.2004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurogenesis from endogenous progenitor cells in the adult forebrain ventricular wall may be induced by the local viral overexpression of cognate neuronal differentiation agents, in particular BDNF. Here, we show that the overexpression of noggin, by acting to inhibit glial differentiation by subependymal progenitor cells, can potentiate adenoviral BDNF-mediated recruitment of new neurons to the adult rat neostriatum. The new neurons survive at least 2 months after their genesis in the subependymal zone and are recruited primarily as GABAergic DARPP-32(+) medium spiny neurons in the caudate-putamen. The new medium spiny neurons successfully project to the globus pallidus, their usual developmental target, extending processes over several millimeters of the normal adult striatum. Thus, concurrent suppression of subependymal glial differentiation and promotion of neuronal differentiation can mobilize endogenous subependymal progenitor cells to achieve substantial neuronal addition to otherwise non-neurogenic regions of the adult brain.
引用
收藏
页码:2133 / 2142
页数:10
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