Galderisi U, Melone M A, Jori F P, Piegari E, Di Bernardo G, Cipollaro M, Cascino A, Peluso G, Claudio P P, Giordano A
Department of Experimental Medicine, Section of Pharmacology, CRISCEB, Second University of Naples, Naples, Italy.
Mol Cell Neurosci. 2001 Mar;17(3):415-25. doi: 10.1006/mcne.2000.0949.
There are many data on the activity of the RB gene in neural differentiation and apoptosis, but the role of pRb2/p130 in neuronal and glial maturation has been far less investigated. To elucidate the role of pRb2/p130 in astrocyte development we overexpressed this protein in astrocytoma and normal astrocyte cultures by adenoviral-mediated gene transfer. In astrocytoma cells, p130/RB2 overexpression resulted in a significant reduction of cell growth and in an increased G(0)/G(1) cell population. We did not observe any induction of programmed cell death as determined by TUNEL reaction. Interestingly, pRb2/p130 overexpression induced astrocyte differentiation. Astrocyte cell cycle arrest and differentiation seemed to proceed through a way distinct from the p53 pathway.
关于RB基因在神经分化和凋亡中的活性有许多数据,但pRb2/p130在神经元和神经胶质细胞成熟中的作用却很少被研究。为了阐明pRb2/p130在星形胶质细胞发育中的作用,我们通过腺病毒介导的基因转移在星形细胞瘤和正常星形胶质细胞培养物中过表达了这种蛋白质。在星形细胞瘤细胞中,p130/RB2过表达导致细胞生长显著减少,G(0)/G(1)期细胞群体增加。通过TUNEL反应测定,我们未观察到任何程序性细胞死亡的诱导。有趣的是,pRb2/p130过表达诱导了星形胶质细胞分化。星形胶质细胞的细胞周期停滞和分化似乎通过一种不同于p53途径的方式进行。