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Cdk2 is critical for proliferation and self-renewal of neural progenitor cells in the adult subventricular zone

机译:Cdk2对于成人脑室下区神经祖细胞的增殖和自我更新至关重要

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摘要

We investigated the function of cyclin-dependent kinase 2 (Cdk2) in neural progenitor cells during postnatal development. Chondroitin sulfate proteoglycan (NG2)–expressing progenitor cells of the subventricular zone (SVZ) show no significant difference in density and proliferation between Cdk2−/− and wild-type mice at perinatal ages and are reduced only in adult Cdk2−/− mice. Adult Cdk2−/− SVZ cells in culture display decreased self-renewal capacity and enhanced differentiation. Compensatory mechanisms in perinatal Cdk2−/− SVZ cells, which persist until postnatal day 15, involve increased Cdk4 expression that results in retinoblastoma protein inactivation. A subsequent decline in Cdk4 activity to wild-type levels in postnatal day 28 Cdk2−/− cells coincides with lower NG2+ proliferation and self-renewal capacity similar to adult levels. Cdk4 silencing in perinatal Cdk2−/− SVZ cells abolishes Cdk4 up-regulation and reduces cell proliferation and self- renewal to adult levels. Conversely, Cdk4 overexpression in adult SVZ cells restores proliferative capacity to wild-type levels. Thus, although Cdk2 is functionally redundant in perinatal SVZ, it is important for adult progenitor cell proliferation and self-renewal through age-dependent regulation of Cdk4.
机译:我们调查了细胞周期蛋白依赖性激酶2(Cdk2)在神经祖细胞在产后发育过程中的功能。在室周下表达Cdk2 -// 的小鼠和野生型小鼠的软骨下区(SVZ)的表达硫酸软骨素蛋白聚糖(NG2)的密度和增殖没有显着差异,并且仅在成年期降低成年Cdk2 -/-小鼠。培养的成年Cdk2 -// SVZ细胞显示出降低的自我更新能力和增强的分化能力。围产期Cdk2 -/- SVZ细胞的补偿机制一直持续到出生后第15天,涉及到Cdk4表达增加,导致成视网膜细胞瘤蛋白失活。在出生后第28天Cdk2 -/-细胞中Cdk4活性随后下降至野生型水平,这与较低的NG2 + 增殖和自我更新能力相近,与成人水平相似。围产期Cdk2 -/- SVZ细胞中的Cdk4沉默消除了Cdk4的上调,并将细胞增殖和自我更新降低到成年水平。相反,成年SVZ细胞中Cdk4的过量表达将增殖能力恢复到野生型水平。因此,尽管Cdk2在围产期SVZ中功能上是多余的,但它对于成年祖细胞增殖和通过年龄依赖性Cdk4调节自我更新很重要。

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