Peunova N, Enikolopov G
Cold Spring Harbor Laboratory, New York 11724, USA.
Nature. 1995 May 4;375(6526):68-73. doi: 10.1038/375068a0.
Arrest of cell division is a prerequisite for cells to enter a program of terminal differentiation. Mitogenesis and cytostasis of neuronal cell precursors can be induced by the same or by different growth or trophic factors. Response of PC12 cells to nerve growth factor (NGF) involves a proliferative phase that is followed by growth arrest and differentiation. Here we present evidence that the cytostatic effect of NGF is mediated by nitric oxide (NO), a second messenger molecule with both para- and autocrine properties that can diffuse freely and act within a restricted volume. We show that NGF induces different forms of nitric oxide synthase (NOS) in neuronal cells, that nitric oxide (NO) acts as a cytostatic agent in these cells, that inhibition of NOS leads to reversal of NGF-induced cytostasis and thereby prevents full differentiation, and that capacity of a mutant cell line to differentiate can be rescued by exogenous NO. We suggest that induction of NOS is an important step in the commitment of neuronal precursors and that NOS serves as a growth arrest gene, initiating the switch to cytostasis during differentiation.
细胞分裂的停滞是细胞进入终末分化程序的一个先决条件。神经元细胞前体的有丝分裂和细胞生长停滞可由相同或不同的生长或营养因子诱导。PC12细胞对神经生长因子(NGF)的反应包括一个增殖阶段,随后是生长停滞和分化。在此我们提供证据表明,NGF的细胞生长停滞效应是由一氧化氮(NO)介导的,NO是一种具有旁分泌和自分泌特性的第二信使分子,它能自由扩散并在有限的空间内起作用。我们表明,NGF在神经元细胞中诱导不同形式的一氧化氮合酶(NOS),一氧化氮(NO)在这些细胞中作为一种细胞生长停滞因子起作用,抑制NOS会导致NGF诱导的细胞生长停滞的逆转,从而阻止完全分化,并且外源性NO可以挽救突变细胞系的分化能力。我们认为,NOS的诱导是神经元前体定向分化的一个重要步骤,并且NOS作为一个生长停滞基因,在分化过程中启动向细胞生长停滞的转变。