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鱼藤酮通过 Lfc/RhoA/ROCK 通路抑制培养海马神经元的轴突生成。

Rotenone inhibits axonogenesis via an Lfc/RhoA/ROCK pathway in cultured hippocampal neurons.

机构信息

Laboratory of Neurobiology, INIMEC-CONICET, Córdoba, Argentina.

Universidad Nacional de Córdoba, Córdoba, Argentina.

出版信息

J Neurochem. 2018 Sep;146(5):570-584. doi: 10.1111/jnc.14547. Epub 2018 Aug 16.

DOI:10.1111/jnc.14547
PMID:29972689
Abstract

Rotenone, a broad-spectrum insecticide, piscicide and pesticide, produces a complete and selective suppression of axonogenesis in cultured hippocampal neurons. This effect is associated with an inhibition of actin dynamics through activation of Ras homology member A (RhoA) activity. However, the upstream signaling mechanisms involved in rotenone-induced RhoA activation were unknown. We hypothesized that rotenone might inhibit axon growth by the activation of RhoA/ROCK pathway because of the changes in microtubule (MT) dynamics and the concomitant release of Lfc, a MT-associated Guanine Nucleotide Exchange Factor (GEF) for RhoA. In this study, we demonstrate that rotenone decreases MT stability in morphologically unpolarized neurons. Taxol (3 nM), a drug that stabilizes MT, attenuates the inhibitory effect of rotenone (0.1 μM) on axon formation. Radiometric Forster Resonance Energy Transfer, revealed that this effect is associated with inhibition of rotenone-induced RhoA and ROCK activation. Interestingly, silencing of Lfc, but not of the RhoA GEF ArhGEF1, prevents the inhibitory effect of rotenone on axon formation. Our results suggest that rotenone-induced MT de-stabilization releases Lfc from MT thereby promoting RhoA and ROCK activities and the consequent inhibition of axon growth. Open Science: This manuscript was awarded with the Open Materials Badge. For more information see: https://cos.io/our-services/open-science-badges/.

摘要

鱼藤酮是一种广谱杀虫剂、杀鱼类药物和农药,它能完全且选择性地抑制培养的海马神经元轴突发生。这种作用与通过激活 Ras 同源物 A(RhoA)活性抑制肌动蛋白动力学有关。然而,鱼藤酮诱导的 RhoA 激活的上游信号机制尚不清楚。我们假设鱼藤酮可能通过激活 RhoA/ROCK 途径来抑制轴突生长,因为微管(MT)动力学的变化和伴随的 Lfc 的释放,Lfc 是一种 MT 相关的鸟嘌呤核苷酸交换因子(GEF),用于 RhoA。在这项研究中,我们证明鱼藤酮降低了形态上未极化神经元中的 MT 稳定性。紫杉醇(3 nM),一种稳定 MT 的药物,可减弱鱼藤酮(0.1 μM)对轴突形成的抑制作用。辐射共振能量转移显示,这种作用与抑制鱼藤酮诱导的 RhoA 和 ROCK 激活有关。有趣的是,沉默 Lfc,但不是 RhoA GEF ArhGEF1,可防止鱼藤酮对轴突形成的抑制作用。我们的结果表明,鱼藤酮诱导的 MT 去稳定化将 Lfc 从 MT 上释放出来,从而促进 RhoA 和 ROCK 活性,并随后抑制轴突生长。开放科学:本文获得了开放材料徽章。有关更多信息,请参见:https://cos.io/our-services/open-science-badges/。

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