RhoA 信号通路对轴突生长和微管动力学的双重时空调控

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-07-15 Epub Date: 2024-07-29 DOI:10.1242/jcs.261970
José Wojnacki, Gonzalo Quassollo, Martín D Bordenave, Nicolás Unsain, Gaby F Martínez, Alan M Szalai, Olivier Pertz, Gregg G Gundersen, Francesca Bartolini, Fernando D Stefani, Alfredo Cáceres, Mariano Bisbal
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引用次数: 0

摘要

RhoA 在神经元极化中起着至关重要的作用,其抑制轴突生长的作用已被深入研究。我们现在报告说,RhoA 对轴突生长不仅有抑制作用,而且还有刺激作用,这取决于其作用的时间和地点以及所涉及的下游效应器。在培养的海马神经元中,FRET 成像显示 RhoA 活性选择性地定位在未分化神经元的生长锥中,而在发育中的轴突中则显示出双相模式,在新生轴突中含量低,而在伸长轴突中含量高。RhoA-Rho激酶(ROCK)信号传导会阻止轴突的启动,但对其伸长没有影响,而甲形蛋白抑制则会减少轴突的伸长,但不会显著改变最初的生长。此外,RhoA-mDia 通过刺激生长锥微管的稳定性和组装来促进轴突的伸长,而 RhoA-ROCK 则抑制生长锥微管的组装和突起。
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Dual spatio-temporal regulation of axon growth and microtubule dynamics by RhoA signaling pathways.

RhoA plays a crucial role in neuronal polarization, where its action restraining axon outgrowth has been thoroughly studied. We now report that RhoA has not only an inhibitory but also a stimulatory effect on axon development depending on when and where exerts its action and the downstream effectors involved. In cultured hippocampal neurons, FRET imaging revealed that RhoA activity selectively localized in growth cones of undifferentiated neurites, whereas in developing axons it displayed a biphasic pattern, being low in nascent axons and high in elongating ones. RhoA-Rho kinase (ROCK) signaling prevented axon initiation but had no effect on elongation, whereas formin inhibition reduced axon extension without significantly altering initial outgrowth. In addition, RhoA-mDia signaling promoted axon elongation by stimulating growth cone microtubule stability and assembly, as opposed to RhoA-ROCK signaling, which restrained growth cone microtubule assembly and protrusion.

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4.30%
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