【2h】

Initiating and Growing an Axon

机译:启动和生长轴突

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摘要

The ability of neurons to form a single axon and multiple dendrites underlies the directional flow of information transfer in the central nervous system. Dendrites and axons are molecularly and functionally distinct domains. Dendrites integrate synaptic inputs, triggering the generation of action potentials at the level of the soma. Action potentials then propagate along the axon, which makes presynaptic contacts onto target cells. This article reviews what is known about the cellular and molecular mechanisms underlying the ability of neurons to initiate and extend a single axon during development. Remarkably, neurons can polarize to form a single axon, multiple dendrites, and later establish functional synaptic contacts in reductionist in vitro conditions. This approach became, and remains, the dominant model to study axon initiation and growth and has yielded the identification of many molecules that regulate axon formation in vitro ( ). At present, only a few of the genes identified using in vitro approaches have been shown to be required for axon initiation and outgrowth in vivo. In vitro, axon initiation and elongation are largely intrinsic properties of neurons that are established in the absence of relevant extracellular cues. However, the importance of extracellular cues to axon initiation and outgrowth in vivo is emerging as a major theme in neural development ( ). In this article, we focus our attention on the extracellular cues and signaling pathways required in vivo for axon initiation and axon extension.
机译:神经元形成单个轴突和多个树突的能力是中枢神经系统中信息传递的定向流的基础。树突和轴突是分子和功能上不同的域。树枝状突触整合了突触输入,触发了躯体水平上动作电位的产生。然后,动作电位沿着轴突传播,这使突触前接触到靶细胞上。本文回顾了有关神经元在发育过程中引发和延伸单个轴突能力的细胞和分子机制的知识。值得注意的是,神经元可以极化形成单个轴突,多个树突,并随后在还原剂体外条件下建立功能性的突触接触。这种方法已经成为并且仍然是研究轴突起始和生长的主要模型,并且已经鉴定出许多体外调节轴突形成的分子。目前,已经证明使用体外方法鉴定的基因中只有少数是体内轴突起始和生长所需的。在体外,轴突的起始和伸长主要是在没有相关细胞外信号的情况下建立的神经元的固有特性。然而,细胞外提示对体内轴突启动和生长的重要性正逐渐成为神经发育的主要主题()。在本文中,我们将注意力集中在轴突起始和轴突延伸在体内所需的细胞外提示和信号传导途径上。

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