Molecular guidance cues necessary for axon pathfinding from the ventral cochlear nucleus
| Autor: | Peter H. Mathers, Albert S. Berrebi, Andrew A. Jarjour, David M. Howell, George A. Spirou, Timothy E. Kennedy, Warren J. Morgan |
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| Rok vydání: | 2007 |
| Předmět: |
Cochlear Nucleus
Auditory Pathways Deleted in Colorectal Cancer Nerve Tissue Proteins Receptors Cell Surface Biology Mice Pregnancy Netrin Animals Nerve Growth Factors Amino Acids Receptors Immunologic In Situ Hybridization Mice Knockout Neurons Tumor Suppressor Proteins General Neuroscience fungi Gene Expression Regulation Developmental Netrin-1 Commissure DCC Receptor Embryo Mammalian Immunohistochemistry Slit Axons nervous system MAFB Superior olivary complex Female Axon guidance Brainstem Neuroscience |
| Zdroj: | The Journal of Comparative Neurology. 504:533-549 |
| ISSN: | 1096-9861 0021-9967 |
| DOI: | 10.1002/cne.21443 |
| Popis: | During development, multiple guidance cues direct the formation of appropriate synaptic connections. Factors that guide developing axons are known for various pathways throughout the mammalian brain; however, signals necessary to establish auditory connections are largely unknown. In the auditory brainstem the neurons whose axons traverse the midline in the ventral acoustic stria (VAS) are primarily located in the ventral cochlear nucleus (VCN) and project bilaterally to the superior olivary complex (SOC). The circumferential trajectory taken by developing VCN axons is similar to that of growing axons of spinal commissural neurons. Therefore, we reasoned that netrin-DCC and slit-robo signaling systems function in the guidance of VCN axons. VCN neurons express the transcription factor, mafB, as early as embryonic day (E) 13.5, thereby identifying the embryonic VCN for these studies. VCN axons extend toward the midline as early as E13, with many axons crossing by E14.5. During this time, netrin-1 and slit-1 RNAs are expressed at the brainstem midline. Additionally, neurons within the VCN express RNA for DCC, robo-1, and robo-2, and axons in the VAS are immunoreactive for DCC. VCN axons do not reach the midline of the brainstem in mice mutant for either the netrin-1 or DCC gene. VCN axons extend in pups lacking netrin-1, but most DCC-mutant samples lack VCN axonal outgrowth. Stereological cell estimates indicate only a modest reduction of VCN neurons in DCC-mutant mice. Taken together, these data show that a functional netrin-DCC signaling system is required for establishing proper VCN axonal projections in the auditory brainstem. J. Comp. Neurol. 504:533–549, 2007. © 2007 Wiley-Liss, Inc. |
| Databáze: | OpenAIRE |
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