神经科学
谷氨酸的
生物
神经发生
大脑皮层
少突胶质细胞
神经干细胞
胶质纤维酸性蛋白
谷氨酸受体
神经胶质
细胞生物学
受体
干细胞
中枢神经系统
髓鞘
免疫学
免疫组织化学
生物化学
作者
Robert Blum,Christophe Heinrich,Rodrigo Sánchez,Alexandra Lepier,Eckart D. Gundelfinger,Benedikt Berninger,Magdalena Götz
出处
期刊:Cerebral Cortex
[Oxford University Press]
日期:2010-06-18
卷期号:21 (2): 413-424
被引量:47
标识
DOI:10.1093/cercor/bhq107
摘要
In the subependymal zone and the dentate gyrus of the adult brain of rodents, neural stem cells with glial properties generate new neurons in a life-long process. The identification of glial progenitors outside the neurogenic niches, oligodendrocyte precursors in the healthy brain, and reactive astrocytes after cortical injury led to the idea of using these cells as endogenous cell source for neural repair in the cerebral cortex. Recently, our group showed that proliferating astroglia from the cerebral cortex can be reprogrammed into neurons capable of action potential firing by forced expression of neurogenic fate determinants but failed to develop synapses. Here, we describe a maturation profile of cultured reprogrammed NG2+ and glial fibrillary acidic protein+ glia cells of the postnatal rat cortex that ends with the establishment of a glutamatergic neuronal network. Within 3 weeks after viral expression of the transcription factor neurogenin 2 (Ngn2), glia-derived neurons exhibit network-driven, glutamate receptor–dependent oscillations in Ca2+ and exhibit functional pre- and postsynaptic specialization. Interestingly, the Ngn2-instructed glutamatergic network also supports the maturation of a γ-aminobutyric acid (GABA)ergic input via GABAA receptors in a non-cell autonomous manner. The "proof-of-principle" results imply that a single transcription factor may be sufficient to instruct a neuronal network from a glia-like cell source.
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