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The Helix-Loop-Helix Protein Id1 Controls Stem Cell Proliferation During Regenerative Neurogenesis in the Adult Zebrafish Telencephalon

机译:Helix-Loop-Helix蛋白ID1在成人斑马鱼斜视蛋白在成人斑马鱼的再生神经发生期间控制干细胞增殖

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摘要

The teleost brain has the remarkable ability to generate new neurons and to repair injuries during adult life stages. Maintaining life-long neurogenesis requires careful management of neural stem cell pools. In a genome-wide expression screen for transcription regulators, the id1 gene, encoding a negative regulator of E-proteins, was found to be upregulated in response to injury. id1 expression was mapped to quiescent type I neural stem cells in the adult telencephalic stem cell niche. Gain and loss of id1 function in vivo demonstrated that Id1 promotes stem cell quiescence. The increased id1 expression observed in neural stem cells in response to injury appeared independent of inflammatory signals, suggesting multiple antagonistic pathways in the regulation of reactive neurogenesis. Together, we propose that Id1 acts to maintain the neural stem cell pool by counteracting neurogenesis-promoting signals.
机译:Textost脑具有显着的能力,可以产生新神经元并在成人生活阶段修复伤害。 维持寿命长的神经发生需要仔细管理神经干细胞库。 在用于转录调节剂的基因组表达筛网中,发现编码E-蛋白的负调节剂的ID1基因是响应于损伤而上调的。 将ID1表达映射到成人视线肺细胞Niche中的静态型I神经干细胞。 体内ID1功能的增益和丧失证明ID1促进干细胞静态。 在神经干细胞中观察到响应于损伤在神经干细胞中观察到的增加的ID1表达,与炎症信号无关,表明在反应性神经发生调节中具有多种拮抗途径。 我们建议ID1通过抵消神经发生促进信号来维持神经干细胞库。

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