Gervasi F, D'Agnano I, Vossio S, Zupi G, Sacchi A, Lombardi D
Laboratorio di Oncogenesi Molecolare, Istituto Regina Elena, Centro Ricerca Sperimentale, Rome, Italy.
Cell Growth Differ. 1996 Dec;7(12):1689-95.
The nm23 genes codify nucleoside diphosphate kinases, which have been shown to be involved in the regulation of microtubule dynamics. We have demonstrated previously that the association between the Nm23-M1 protein and cytoskeletal beta-tubulin correlates with cell differentiation. It is known that microtubules and microtubule-associated proteins are fundamental elements regulating neuronal differentiation. In the present study, we have investigated the ability of nm23 to influence nerve growth factor-induced PC12 cell differentiation. To this end, we have altered PC12 intracellular levels of nm23-M1 by means of sense and antisense transfections. In the presence of nerve growth factor, overexpression of nm23 delays cell cycle transition, rapidly induces neurite outgrowth, and increases the expression of neurofilament and microtubule proteins. On the contrary, down-regulation of nm23 enhances cell proliferation and inhibits neuronal differentiation. These findings indicate that neuronal cell proliferation and differentiation can be modulated by nm23 expression levels.
nm23基因编码核苷二磷酸激酶,该激酶已被证明参与微管动力学的调节。我们之前已经证明,Nm23-M1蛋白与细胞骨架β-微管蛋白之间的关联与细胞分化相关。众所周知,微管和微管相关蛋白是调节神经元分化的基本要素。在本研究中,我们研究了nm23影响神经生长因子诱导的PC12细胞分化的能力。为此,我们通过正义和反义转染改变了PC12细胞内nm23-M1的水平。在神经生长因子存在的情况下,nm23的过表达延迟细胞周期转变,迅速诱导神经突生长,并增加神经丝和微管蛋白的表达。相反,nm23的下调增强细胞增殖并抑制神经元分化。这些发现表明,神经元细胞的增殖和分化可由nm23的表达水平调节。