首页> 美国卫生研究院文献>Biochemical Journal >RB2/p130 ectopic gene expression in neuroblastoma stem cells: evidence of cell-fate restriction and induction of differentiation.
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RB2/p130 ectopic gene expression in neuroblastoma stem cells: evidence of cell-fate restriction and induction of differentiation.

机译:RB2 / p130异位基因在神经母细胞瘤干细胞中的表达:细胞命运限制和分化诱导的证据。

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摘要

The activity of the RB2/p130 gene, which is a member of the retinoblastoma gene family, is cell-cycle-regulated and plays a key role in growth inhibition and differentiation. We used neuroblastoma cell lines as a model for studies on neural crest progenitor cell differentiation. We show that Rb2/p130 ectopic protein expression induces morphological and molecular modifications, promoting differentiation of intermediate (I) phenotype SK-N-BE(2)-C neuroblastoma cells towards a neuroblastic (N) rather than a Schwann/glial/melanocytic (S) phenotype. These modifications are stable as they persist even after treatment with an S-phenotype inducer. Rb2/p130 ectopic expression also induces a more differentiated phenotype in N-type SH-SY-5Y cells. Further, this function appears to be independent of cell-cycle withdrawal. The data reported suggest that the Rb2/p130 protein is able to induce neuronal lineage specification and differentiation in neural crest stem and committed neuroblastoma cells, respectively. Thus, the Rb2/p130 protein seems to be required throughout the full neural maturation process.
机译:RB2 / p130基因是视网膜母细胞瘤基因家族的成员,其活性受到细胞周期的调节,在生长抑制和分化中起关键作用。我们使用神经母细胞瘤细胞系作为神经rest祖细胞分化研究的模型。我们显示Rb2 / p130异位蛋白表达诱导形态和分子修饰,促进中间(I)表型SK-N-BE(2)-C神经母细胞瘤细胞向神经母细胞(N)分化,而不是向Schwann /神经胶质细胞/黑素细胞( S)表型。这些修饰是稳定的,因为它们甚至在用S型表型诱导剂治疗后仍持续存在。 Rb2 / p130异位表达还在N型SH-SY-5Y细胞中诱导了更高分化的表型。此外,该功能似乎与细胞周期退出无关。报告的数据表明,Rb2 / p130蛋白能够分别诱导神经c干细胞和定型神经母细胞瘤细胞的神经元谱系分化。因此,似乎在整个神经成熟过程中都需要Rb2 / p130蛋白。

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