Initiating and Growing an Axon

被引:117
作者
Polleux, F. [1 ]
Snider, William [1 ]
机构
[1] Univ N Carolina, Ctr Neurosci, Chapel Hill, NC 27599 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY | 2010年 / 2卷 / 04期
关键词
N-TERMINAL KINASE; MICROTUBULE-ASSOCIATED PROTEINS; UBIQUITIN-PROTEASOME SYSTEM; ADENOMATOUS POLYPOSIS-COLI; HIPPOCAMPAL NEURONAL POLARITY; SERIAL SECTION ANALYSIS; RETINAL GANGLION-CELLS; C-JUN; IN-VIVO; CORTICAL-NEURONS;
D O I
10.1101/cshperspect.a001925
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
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 (Dotti et al. 1988). 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 (Barnes and Polleux 2009). In this article, we focus our attention on the extracellular cues and signaling pathways required in vivo for axon initiation and axon extension.
引用
收藏
页数:19
相关论文
共 173 条
[1]   UNC-6/Netrin induces neuronal asymmetry and defines the site of axon formation [J].
Adler, CE ;
Fetter, RD ;
Bargmann, CI .
NATURE NEUROSCIENCE, 2006, 9 (04) :511-518
[2]   Bcl-2 family regulation of neuronal development and neurodegeneration [J].
Akhtar, RS ;
Ness, JM ;
Roth, KA .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2004, 1644 (2-3) :189-203
[3]   Adenomatous polyposis coli (APC):: a multi-functional tumor suppressor gene [J].
Aoki, Koji ;
Taketo, Makoto M. .
JOURNAL OF CELL SCIENCE, 2007, 120 (19) :3327-3335
[4]   Synaptic Drosophila UNC-13 is regulated by antagonistic G-protein pathways via a proteasome-dependent degradation mechanism [J].
Aravamudan, B ;
Broadie, K .
JOURNAL OF NEUROBIOLOGY, 2003, 54 (03) :417-438
[5]   Role of CRMP-2 in neuronal polarity [J].
Arimura, N ;
Menager, C ;
Fukata, Y ;
Kaibuchi, K .
JOURNAL OF NEUROBIOLOGY, 2004, 58 (01) :34-47
[6]   Neuronal polarity: from extracellular signals to intracellular mechanisms [J].
Arimura, Nariko ;
Kaibuchi, Kozo .
NATURE REVIEWS NEUROSCIENCE, 2007, 8 (03) :194-205
[7]   LKB1 regulates neuronal migration and neuronal differentiation in the developing neocortex through centrosomal positioning [J].
Asada, Naoyuki ;
Sanada, Kamon ;
Fukada, Yoshitaka .
JOURNAL OF NEUROSCIENCE, 2007, 27 (43) :11769-11775
[8]   New sights into the molecular mechanisms specifying neuronal polarity in vivo [J].
Barnes, Anthony P. ;
Solecki, David ;
Polleux, Franck .
CURRENT OPINION IN NEUROBIOLOGY, 2008, 18 (01) :44-52
[9]   LKB1 and SAD kinases define a pathway required for the polarization of cortical neurons [J].
Barnes, Anthony P. ;
Lilley, Brendan N. ;
Pan, Y. Albert ;
Plummer, Lisa J. ;
Powell, Ashton W. ;
Raines, Alexander N. ;
Sanes, Joshua R. ;
Polleux, Franck .
CELL, 2007, 129 (03) :549-563
[10]   Establishment of Axon-Dendrite Polarity in Developing Neurons [J].
Barnes, Anthony P. ;
Polleux, Franck .
ANNUAL REVIEW OF NEUROSCIENCE, 2009, 32 :347-381