Department of Physiology, Medical School, University of Patras, Patras, Greece.
Stem Cells. 2011 Aug;29(8):1269-82. doi: 10.1002/stem.678.
During cortical development, coordination of proliferation and differentiation ensures the timely generation of different neural progenitor lineages that will give rise to mature neurons and glia. Geminin is an inhibitor of DNA replication and it has been proposed to regulate cell proliferation and fate determination during neurogenesis via interactions with transcription factors and chromatin remodeling complexes. To investigate the in vivo role of Geminin in the maintenance and differentiation of cortical neural progenitors, we have generated mice that lack Geminin expression in the developing cortex. Our results show that loss of Geminin leads to the expansion of neural progenitor cells located at the ventricular and subventricular zones of the developing cortex. Early cortical progenitors lacking Geminin exhibit a longer S-phase and a reduced ability to generate early born neurons, consistent with a preference on self-renewing divisions. Overexpression of Geminin in progenitor cells of the cortex reduces the number of neural progenitor cells, promotes cell cycle exit and subsequent neuronal differentiation. Our study suggests that Geminin has an important role during cortical development in regulating progenitor number and ultimately neuron generation.
在皮质发育过程中,增殖和分化的协调确保了不同神经祖细胞谱系的及时产生,这些谱系将产生成熟的神经元和神经胶质细胞。Geminin 是 DNA 复制的抑制剂,它通过与转录因子和染色质重塑复合物的相互作用,被提议调节神经发生过程中的细胞增殖和命运决定。为了研究 Geminin 在皮质神经祖细胞的维持和分化中的体内作用,我们生成了在发育中的皮质中缺乏 Geminin 表达的小鼠。我们的结果表明,Geminin 的缺失导致位于发育中的皮质脑室和室下区的神经祖细胞的扩增。缺乏 Geminin 的早期皮质祖细胞表现出更长的 S 期和减少产生早期出生神经元的能力,这与自我更新分裂的偏好一致。Geminin 在皮质祖细胞中的过表达减少了神经祖细胞的数量,促进了细胞周期退出和随后的神经元分化。我们的研究表明,Geminin 在皮质发育过程中在调节祖细胞数量和最终神经元产生方面起着重要作用。