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神经母细胞基因 2 诱导成年室管膜下区神经祖细胞向谷氨酸能神经元谱系分化。

Programming of neural progenitors of the adult subependymal zone towards a glutamatergic neuron lineage by neurogenin 2.

机构信息

Research Group "Adult Neurogenesis and Cellular Reprogramming", Institute of Physiological Chemistry, University Medical Center Johannes Gutenberg University, Mainz, Germany; Centre for Developmental Neurobiology, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.

Physiological Genomics, Institute of Physiology, Ludwig-Maximilians University Munich, Munich, Germany.

出版信息

Stem Cell Reports. 2023 Dec 12;18(12):2418-2433. doi: 10.1016/j.stemcr.2023.10.019. Epub 2023 Nov 22.

Abstract

Although adult subependymal zone (SEZ) neural stem cells mostly generate GABAergic interneurons, a small progenitor population expresses the proneural gene Neurog2 and produces glutamatergic neurons. Here, we determined whether Neurog2 could respecify SEZ neural stem cells and their progeny toward a glutamatergic fate. Retrovirus-mediated expression of Neurog2 induced the glutamatergic lineage markers TBR2 and TBR1 in cultured SEZ progenitors, which differentiated into functional glutamatergic neurons. Likewise, Neurog2-transduced SEZ progenitors acquired glutamatergic neuron hallmarks in vivo. Intriguingly, they failed to migrate toward the olfactory bulb and instead differentiated within the SEZ or the adjacent striatum, where they received connections from local neurons, as indicated by rabies virus-mediated monosynaptic tracing. In contrast, lentivirus-mediated expression of Neurog2 failed to reprogram early SEZ neurons, which maintained GABAergic identity and migrated to the olfactory bulb. Our data show that NEUROG2 can program SEZ progenitors toward a glutamatergic identity but fails to reprogram their neuronal progeny.

摘要

尽管成年室管膜下区(SEZ)神经干细胞主要产生 GABA 能中间神经元,但一小部分祖细胞表达神经前体细胞基因 Neurog2 并产生谷氨酸能神经元。在这里,我们确定 Neurog2 是否可以重新编程 SEZ 神经干细胞及其祖细胞向谷氨酸能命运分化。逆转录病毒介导的 Neurog2 表达诱导培养的 SEZ 祖细胞中的谷氨酸能谱系标记物 TBR2 和 TBR1,这些祖细胞分化为功能性谷氨酸能神经元。同样,Neurog2 转导的 SEZ 祖细胞在体内获得了谷氨酸能神经元的特征。有趣的是,它们未能向嗅球迁移,而是在 SEZ 或相邻的纹状体中分化,在那里它们通过狂犬病毒介导的单突触追踪与局部神经元建立联系。相比之下,慢病毒介导的 Neurog2 表达未能重新编程早期 SEZ 神经元,这些神经元保持 GABA 能特性并迁移到嗅球。我们的数据表明,Neurog2 可以将 SEZ 祖细胞编程为谷氨酸能特性,但不能重新编程其神经元祖细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d3f/10724369/0c2760b66594/fx1.jpg

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