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源自胚胎皮质的内源性因子调节出生后脑室下区细胞培养物的增殖和神经元分化。

Endogenous factors derived from embryonic cortex regulate proliferation and neuronal differentiation of postnatal subventricular zone cell cultures.

作者信息

Agasse Fabienne, Benzakour Omar, Berjeaud Jean-Marc, Roger Michel, Coronas Valérie

机构信息

CNRS, UMR 6187, Institut de Physiologie et Biologie Cellulaires, Université de Poitiers, France.

出版信息

Eur J Neurosci. 2006 Apr;23(8):1970-6. doi: 10.1111/j.1460-9568.2006.04739.x.

DOI:10.1111/j.1460-9568.2006.04739.x
PMID:16630045
Abstract

In rodents, the subventricular zone (SVZ) harbours neural stem cells that proliferate and produce neurons throughout life. Previous studies showed that factors released by the developing cortex promote neurogenesis in the embryonic ventricular zone. In the present report, we studied in the rat the possible involvement of endogenous factors derived from the embryonic cortex in the regulation of the development of postnatal SVZ cells. To this end, SVZ neurospheres were maintained with explants or conditioned media (CM) prepared from embryonic day (E) 13, E16 or early postnatal cortex. We demonstrate that early postnatal cortex-derived factors have no significant effect on SVZ cell proliferation or differentiation. In contrast, E13 and E16 cortex release diffusible, heat-labile factors that promote SVZ cell expansion through increased proliferation and reduced cell death. In addition, E16 cortex-derived factors stimulate neuronal differentiation in both early postnatal and adult SVZ cultures. Fibroblast growth factor (FGF)-2- but not epidermal growth factor (EGF)-immunodepletion drastically reduces the mitogenic effect of E16 cortex CM, hence suggesting a major role of endogenous FGF-2 released by E16 cortex in the stimulation of SVZ cell proliferation. The evidence we provide here for the regulation of SVZ cell proliferation and neuronal differentiation by endogenous factors released from embryonic cortex may be of major importance for brain repair research.

摘要

在啮齿动物中,脑室下区(SVZ)含有神经干细胞,这些细胞在整个生命过程中都会增殖并产生神经元。先前的研究表明,发育中的皮质释放的因子可促进胚胎脑室区的神经发生。在本报告中,我们在大鼠中研究了源自胚胎皮质的内源性因子在调节出生后SVZ细胞发育中的可能作用。为此,将SVZ神经球与从胚胎第(E)13天、E16天或出生后早期皮质制备的外植体或条件培养基(CM)一起培养。我们证明,出生后早期皮质衍生的因子对SVZ细胞增殖或分化没有显著影响。相比之下,E13和E16皮质释放可扩散的、热不稳定的因子,这些因子通过增加增殖和减少细胞死亡来促进SVZ细胞扩增。此外,E16皮质衍生的因子在出生后早期和成年SVZ培养物中均刺激神经元分化。成纤维细胞生长因子(FGF)-2而非表皮生长因子(EGF)的免疫耗竭可显著降低E16皮质CM的促有丝分裂作用,因此表明E16皮质释放的内源性FGF-2在刺激SVZ细胞增殖中起主要作用。我们在此提供的关于胚胎皮质释放的内源性因子对SVZ细胞增殖和神经元分化的调节的证据,可能对脑修复研究具有重要意义。

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