Kim Yoonju, Lee Sang-Eun, Park Joohyun, Kim Minhyung, Lee Boyoon, Hwang Daehee, Chang Sunghoe
From the Department of Physiology and Biomedical Sciences, Neuroscience Research Institute, Medical Research Center, Biomembrane Plasticity Research Center, and.
From the Department of Physiology and Biomedical Sciences, Biomembrane Plasticity Research Center, and.
J Biol Chem. 2015 Mar 20;290(12):7323-35. doi: 10.1074/jbc.M114.634527. Epub 2015 Jan 20.
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.
最近的研究报告了关于ARF6在树突棘发育中作用的相互矛盾的结果,但对于这一争议尚无明确答案。我们发现,ADP核糖基化因子6(ARF6)根据神经元的成熟度和活性对树突棘的形成起到正向或负向调节作用。ARF6激活增加了发育中神经元的树突棘形成,而在成熟神经元中则降低了树突棘密度。全基因组微阵列分析显示,每个阶段的ARF6激活都会导致参与神经元形态的一组基因呈现相反的表达模式。在两个阶段中,通过磷脂酶D途径的ARF6介导的Rac1激活都是共同因素,但在成熟阶段,拮抗的RhoA途径也参与其中。此外,使用河豚毒素阻断发育中神经元的活性,或使用印防己毒素或化学性长时程增强来增强成熟神经元的活性,均可逆转ARF6对每个阶段的影响。因此,ARF6介导的脊柱结构的活动依赖性动态变化可能在成熟神经元的结构可塑性中发挥作用。