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Signalling mechanisms regulating axonal branching in vivo

机译:体内调节轴突分支的信号传导机制

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摘要

Identification of the molecular mechanisms underlying axonal branching in vivo has begun in several neuronal systems, notably the projections formed by dorsal root ganglion (DRG) neurons or retinal ganglion cells (RGC). cGMP signalling is essential for sensory axon bifurcation at the spinal cord, whereas brain-derived neurotrophic factor (BDNF) and ephrinA signalling establish position-dependent branching of RGC axons. In the latter system, the degradation of specific signalling components, via the ubiquitin-proteasome system, may provide an additional mechanism involved in axon branching of RGC. The process of arborisation is essential for neurons to innervate multiple targets and to build topographic maps. The various forms of branching found in different types of neurons are regulated by distinct signalling pathways activated by multiple extracellular cues in addition to axonal guidance factors. These signalling cascades, together with transcriptional programs, most likely interact and trigger the polymerisation or depolymerisation of the actin and tubulin cytoskeleton to regulate branching.
机译:体内轴突分支的分子机制的鉴定已经在几种神经元系统中开始,尤其是由背根神经节(DRG)神经元或视网膜神经节细胞(RGC)形成的突起。 cGMP信号传导对于脊髓的感觉轴突分叉至关重要,而脑源性神经营养因子(BDNF)和ephrinA信号传导则建立了RGC轴突的位置依赖性分支。在后一种系统中,特定信号成分通过泛素-蛋白酶体系统的降解可提供涉及RGC轴突分支的其他机制。树木化的过程对于神经元神经化多个目标并构建地形图至关重要。在不同类型的神经元中发现的各种形式的分支受轴突引导因子以外的多种细胞外信号激活的不同信号通路的调控。这些信号级联与转录程序最可能相互作用并触发肌动蛋白和微管蛋白细胞骨架的聚合或解聚,以调节分支。

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