Pinto Luisa, Mader Michael T, Irmler Martin, Gentilini Marco, Santoni Federico, Drechsel Daniela, Blum Robert, Stahl Ronny, Bulfone Alessandro, Malatesta Paolo, Beckers Johannes, Götz Magdalena
Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Institute of Stem Cell Research, Ingolstädter Landstr. 1, 85764 Neuherberg/Munich, Germany.
Mol Cell Neurosci. 2008 May;38(1):15-42. doi: 10.1016/j.mcn.2008.01.012. Epub 2008 Feb 1.
Since the discovery of radial glia as the source of neurons, their heterogeneity in regard to neurogenesis has been described by clonal and time-lapse analysis in vitro. However, the molecular determinants specifying neurogenic radial glia differently from radial glia that mostly self-renew remain ill-defined. Here, we isolated two radial glial subsets that co-exist at mid-neurogenesis in the developing cerebral cortex and their immediate progeny. While one subset generates neurons directly, the other is largely non-neurogenic but also gives rise to Tbr2-positive basal precursors, thereby contributing indirectly to neurogenesis. Isolation of these distinct radial glia subtypes allowed determining interesting differences in their transcriptome. These transcriptomes were also strikingly different from the transcriptome of radial glia isolated at the end of neurogenesis. This analysis therefore identifies, for the first time, the lineage origin of basal progenitors and the molecular differences of this lineage in comparison to directly neurogenic and gliogenic radial glia.
自从发现放射状胶质细胞是神经元的来源以来,它们在神经发生方面的异质性已通过体外克隆和延时分析得以描述。然而,与大多进行自我更新的放射状胶质细胞不同,决定神经源性放射状胶质细胞的分子决定因素仍不明确。在此,我们分离出了在发育中的大脑皮层神经发生中期共存的两个放射状胶质细胞亚群及其直接后代。其中一个亚群直接产生神经元,另一个亚群在很大程度上不具有神经源性,但也能产生Tbr2阳性的基底前体细胞,从而间接促进神经发生。分离这些不同的放射状胶质细胞亚型能够确定它们转录组中有趣的差异。这些转录组也与神经发生末期分离出的放射状胶质细胞的转录组显著不同。因此,该分析首次确定了基底祖细胞的谱系起源以及该谱系与直接神经源性和胶质源性放射状胶质细胞相比的分子差异。