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Cortical Neuron Migration and Dendrite Morphology are Regulated by Carboxypeptidase E

机译:Cortical神经元迁移和树突形态由羧肽酶e调节

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摘要

Higher brain function relies on proper development of the cerebral cortex, including correct positioning of neurons and dendrite morphology. Disruptions in these processes may result in various neurocognitive disorders. Mutations in the CPE gene, which encodes carboxypeptidase E (CPE), have been linked to depression and intellectual disability. However, it remains unclear whether CPE is involved in early brain development and in turn contributes to the pathophysiology of neurocognitive disorders. Here, we investigate the effects of CPE knockdown on early brain development and explore the functional significance of the interaction between CPE and its binding partner p150(Glued). We demonstrate that CPE is required for cortical neuron migration and dendrite arborization. Furthermore, we show that expression of CPE-C10 redistributes p150(Glued) from the centrosome and that disruption of CPE interaction with p150(Glued) leads to abnormal neuronal migration and dendrite morphology, suggesting that a complex between CPE and p150(Glued) is necessary for proper neurodevelopment.
机译:更高的脑功能依赖于脑皮层的适当发展,包括神经元和枝晶形态的正确定位。这些过程中断可能导致各种神经认知障碍。编码羧肽酶E(CPE)的CPE基因中的突变与抑郁和智力残疾有关。然而,仍然尚不清楚CPE是否参与早期大脑发育,又有助于神经认知障碍的病理生理学。在这里,我们调查CPE敲低对早期脑发育的影响,探讨CPE与其结合伴侣P150(胶合)之间相互作用的功能意义。我们证明了皮质神经元迁移和树突树脂族需要CPE。此外,我们表明CPE-C10的表达再分配来自中心组体的P150(胶合),并且与P150(胶合)的CPE相互作用的破坏导致神经元迁移和树突形态异常,表明CPE和P150(胶合)之间的复杂性适当的神经发作。

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