Race H M, Wagner J A
J Neurochem. 1985 May;44(5):1588-92. doi: 10.1111/j.1471-4159.1985.tb08799.x.
Published experiments both support and contradict the hypothesis that nerve growth factor (NGF) can regulate adenylate cyclase activity. Using a sensitive assay that measures the conversion of [2-3H]adenine to [3H]cyclic AMP, we have shown that NGF alone cannot measurably stimulate cyclic AMP production, whereas the adenosine analog phenylisopropyladenosine (PIA) stimulates adenylate cyclase 20-fold over basal activity. NGF potentiates the capacity of both PIA and cholera toxin to stimulate cyclic AMP accumulation at all concentrations tested. This potentiation occurs at the earliest measurable times and does not require RNA synthesis. Therefore, we conclude that cyclase activation alone does not account for the effect of NGF on cyclic AMP accumulation and we discuss possible mechanisms.
已发表的实验既支持又反驳了神经生长因子(NGF)可调节腺苷酸环化酶活性这一假说。通过一种灵敏的检测方法来测量[2-³H]腺嘌呤向[³H]环磷酸腺苷(cAMP)的转化,我们发现单独使用NGF无法显著刺激cAMP的产生,而腺苷类似物苯异丙基腺苷(PIA)可使腺苷酸环化酶的活性比基础活性提高20倍。在所有测试浓度下,NGF均可增强PIA和霍乱毒素刺激cAMP积累的能力。这种增强作用在最早可测量的时间就会出现,且不需要RNA合成。因此,我们得出结论,仅环化酶激活并不能解释NGF对cAMP积累的影响,我们还讨论了可能的机制。