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次级树突发育的精细调控:蜕皮激素受体对果蝇胸段中枢神经系统成年神经元谱系的影响。

Fine-tuning of secondary arbor development: the effects of the ecdysone receptor on the adult neuronal lineages of the Drosophila thoracic CNS.

作者信息

Brown Heather L D, Truman James W

机构信息

Department of Biology, University of Washington, Seattle, WA 98195, USA.

出版信息

Development. 2009 Oct;136(19):3247-56. doi: 10.1242/dev.039859. Epub 2009 Aug 26.

Abstract

The adult central nervous system (CNS) of Drosophila is largely composed of relatively homogenous neuronal classes born during larval life. These adult-specific neuron lineages send out initial projections and then arrest development until metamorphosis, when intense sprouting occurs to establish the massive synaptic connections necessary for the behavior and function of the adult fly. In this study, we identified and characterized specific lineages in the adult CNS and described their secondary branch patterns. Because prior studies show that the outgrowth of incumbent remodeling neurons in the CNS is highly dependent on the ecdysone pathway, we investigated the role of ecdysone in the development of the adult-specific neuronal lineages using a dominant-negative construct of the ecdysone receptor (EcR-DN). When EcR-DN was expressed in clones of the adult-specific lineages, neuroblasts persisted longer, but we saw no alteration in the initial projections of the lineages. Defects were observed in secondary arbors of adult neurons, including clumping and cohesion of fine branches, misrouting, smaller arbors and some defasciculation. The defects varied across the multiple neuron lineages in both appearance and severity. These results indicate that the ecdysone receptor complex influences the fine-tuning of connectivity between neuronal circuits, in conjunction with other factors driving outgrowth and synaptic partnering.

摘要

果蝇的成年中枢神经系统(CNS)主要由幼虫期产生的相对同质的神经元类别组成。这些成年特异性神经元谱系发出初始投射,然后停止发育,直到变态期,此时会发生强烈的出芽,以建立成年果蝇行为和功能所需的大量突触连接。在本研究中,我们鉴定并表征了成年CNS中的特定谱系,并描述了它们的二级分支模式。由于先前的研究表明,CNS中现有重塑神经元的生长高度依赖于蜕皮激素途径,我们使用蜕皮激素受体(EcR-DN)的显性负构建体研究了蜕皮激素在成年特异性神经元谱系发育中的作用。当EcR-DN在成年特异性谱系的克隆中表达时,神经母细胞持续时间更长,但我们未观察到谱系初始投射的改变。在成年神经元的二级树突中观察到缺陷,包括细分支的聚集和粘连、错路、较小的树突和一些脱束。这些缺陷在多个神经元谱系中的外观和严重程度各不相同。这些结果表明,蜕皮激素受体复合物与驱动生长和突触配对的其他因素一起,影响神经元回路之间连接性的微调。

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