Contactin-4 Mediates Axon-Target Specificity and Functional Development of the Accessory Optic System

被引:87
作者
Osterhout, Jessica A. [1 ]
Stafford, Benjamin K. [1 ,2 ]
Nguyen, Phong L. [1 ,2 ]
Yoshihara, Yoshihiro [4 ]
Huberman, Andrew D. [1 ,2 ,3 ]
机构
[1] Univ Calif San Diego, Div Biol Sci, Neurobiol Sect, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, Neurosci Dept, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Sch Med, Dept Ophthalmol, La Jolla, CA 92093 USA
[4] RIKEN, Brain Sci Inst, Wako, Saitama 3510198, Japan
基金
美国国家科学基金会;
关键词
RETINAL GANGLION-CELLS; AMYLOID PRECURSOR PROTEIN; MOLECULAR-MECHANISMS; SYNAPTIC LAMINAE; GENETIC-ANALYSIS; MOUSE RETINA; PROJECTIONS; EXPERIENCE; EXPRESSION; SYNAPSES;
D O I
10.1016/j.neuron.2015.04.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The mammalian eye-to-brain pathway includes more than 20 parallel circuits, each consisting of precise long-range connections between specific sets of retinal ganglion cells (RGCs) and target structures in the brain. The mechanisms that drive assembly of these parallel connections and the functional implications of their specificity remain unresolved. Here we show that in the absence of contactin 4 (CNTN4) or one of its binding partners, amyloid precursor protein (APP), a subset of direction-selective RGCs fail to target the nucleus of the optic tract (NOT)-the accessory optic system (AOS) target controlling horizontal image stabilization. Conversely, ectopic expression of CNTN4 biases RGCs to arborize in the NOT, and that process also requires APP. Our data reveal critical and novel roles for CNTN4/APP in promoting target-specific axon arborization, and they highlight the importance of this process for functional development of a behaviorally relevant parallel visual pathway.
引用
收藏
页码:985 / 999
页数:15
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