首页> 美国卫生研究院文献>The Journal of Biological Chemistry >ADP-ribosylation Factor 6 (ARF6) Bidirectionally Regulates Dendritic Spine Formation Depending on Neuronal Maturation and Activity
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ADP-ribosylation Factor 6 (ARF6) Bidirectionally Regulates Dendritic Spine Formation Depending on Neuronal Maturation and Activity

机译:ADP-核糖基化因子6(ARF6)双向调节树突棘的形成取决于神经元的成熟和活动

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摘要

Recent studies have reported conflicting results regarding the role of ARF6 in dendritic spine development, but no clear answer for the controversy has been suggested. We found that ADP-ribosylation factor 6 (ARF6) either positively or negatively regulates dendritic spine formation depending on neuronal maturation and activity. ARF6 activation increased the spine formation in developing neurons, whereas it decreased spine density in mature neurons. Genome-wide microarray analysis revealed that ARF6 activation in each stage leads to opposite patterns of expression of a subset of genes that are involved in neuronal morphology. ARF6-mediated Rac1 activation via the phospholipase D pathway is the coincident factor in both stages, but the antagonistic RhoA pathway becomes involved in the mature stage. Furthermore, blocking neuronal activity in developing neurons using tetrodotoxin or enhancing the activity in mature neurons using picrotoxin or chemical long term potentiation reversed the effect of ARF6 on each stage. Thus, activity-dependent dynamic changes in ARF6-mediated spine structures may play a role in structural plasticity of mature neurons.
机译:最近的研究报道了有关ARF6在树突棘发育中的作用的相互矛盾的结果,但是对于这一争议没有给出明确的答案。我们发现,ADP-核糖基化因子6(ARF6)可以正向或负向调节树突棘的形成,具体取决于神经元的成熟和活性。 ARF6激活增加了发育中神经元的脊柱形成,而降低了成熟神经元中的脊柱密度。全基因组微阵列分析表明,每个阶段的ARF6激活都会导致神经元形态学中的一部分基因表达的相反模式。 ARF6介导的通过磷脂酶D途径激活Rac1是两个阶段的重合因素,但拮抗性RhoA途径却参与了成熟阶段。此外,使用河豚毒素阻断发育中的神经元的神经元活性,或使用皮毒素或化学长期增强作用增强成熟神经元的活性,可以逆转ARF6在每个阶段的作用。因此,ARF6介导的脊柱结构中依赖活动的动态变化可能在成熟神经元的结构可塑性中起作用。

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