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首页> 外文期刊>Nature Communications >Speed control for neuronal migration in the postnatal brain by Gmip-mediated local inactivation of RhoA
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Speed control for neuronal migration in the postnatal brain by Gmip-mediated local inactivation of RhoA

机译:通过Gmip介导的RhoA局部失活来控制出生后大脑中神经元迁移的速度

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摘要

Throughout life, new neurons generated in the ventricular-subventricular zone take the long journey to the olfactory bulb. The intracellular mechanisms that precisely control the neurons' migration speed, enabling their well-organized movement, remain unclear. Rho signalling is known to affect the morphology and movement of various cell types, including neurons. Here we identify Gem-interacting protein (Gmip), a RhoA-specific GTPase-activating protein, as a key factor in saltatory neuronal migration. RhoA is activated at the proximal leading process of migrating neurons, where Gmip is also localized and negatively regulates RhoA. Gmip controls the saltatory movement of neurons that regulate their migration speed and 'stop' positions in the olfactory bulb, thereby altering the neural circuitry. This study demonstrates that Gmip serves as a brake for the RhoA-mediated movement of neuronal somata, and highlights the significance of speed control in the well-organized neuronal migration and the maintenance of neuronal circuits in the postnatal brain.RI ENOMOTO, Atsushi/I-7272-2014
机译:在整个生命过程中,在心室-心室下区产生的新神经元需要很长的一段路程才能到达嗅球。目前尚不清楚精确控制神经元迁移速度,使其组织良好的运动的细胞内机制。已知Rho信号会影响各种细胞类型(包括神经元)的形态和运动。在这里,我们确定了Gem相互作用蛋白(Gmip),一种RhoA特异性GTPase激活蛋白,是盐碱化神经元迁移的关键因素。 RhoA在迁移神经元的近端前导过程中被激活,在该过程中,Gmip也被定位并负向调节RhoA。 Gmip控制神经元的盐分运动,从而调节其在嗅球中的迁移速度和“停止”位置,从而改变神经回路。这项研究表明Gmip可以作为RhoA介导的神经元躯体运动的制动器,并强调了速度控制在出生后大脑组织良好的神经元迁移和神经元回路的维持中的重要性.RI ENOMOTO,Atsushi / I -7272-2014

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