Interplay between the antimetastatic nm23 and the Retinoblastoma-related Rb2/p130 genes in promoting neuronal differentiation of PC12 cells

被引:31
作者
Lombardi, D
Palescandolo, E
Giordano, A
Paggi, MG
机构
[1] Univ Aquila, Dept Expt Med, I-67100 Laquila, Italy
[2] Regina Elena Inst Canc Res, Ctr Exptl Res, Lab Cell Metab & Pharmacokinet, I-00158 Rome, Italy
[3] Thomas Jefferson Univ, Jefferson Med Coll, Dept Pathol, Philadelphia, PA 19107 USA
[4] Thomas Jefferson Univ, Jefferson Med Coll, Dept Anat & Cell Biol, Philadelphia, PA 19107 USA
关键词
nm23; metastasis; retinoblastoma gene family; Rb2/p130; cell cycle; growth arrest; pheochromocytoma PC12 cell line; neuronal differentiation;
D O I
10.1038/sj.cdd.4400842
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Increasing evidence indicates that the nm23 genes, initially documented as suppressors of metastasis progression, are involved in normal development and differentiation. We have shown previously that the murine nm23 gene enhances pheochromocytoma PC12 cells responsiveness to NGF by accelerating cell growth arrest and neurite outgrowth, The present study was aimed at elucidating the mechanisms by which nm23 controls cell proliferation and promotes neuronal differentiation, We demonstrated that nm23 modulates the expression of the Rb2/p130 gene, a negative regulator of cell cycle progression also implicated in the maintenance of the differentiated state, Furthermore, we showed that nm23-H1 mutants, defective in inhibiting the invasive phenotype, downregulate Rb2/p130 expression and inhibit NGF-induced pC12 cell differentiation. in synthesis, our results provide first evidence of Interplay between the nm23 and the Rb2/p130 genes in driving PC12 cells neuronal differentiation and suggest that the antimetastatic and the differentiative nm23 functions can have similar features.
引用
收藏
页码:470 / 476
页数:7
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