EphA4 misexpression alters tonotopic projections in the auditory brainstem

Auditory pathways contain orderly representations of frequency selectivity, which begin at the cochlea and are transmitted to the brainstem via topographically ordered axonal pathways. The mechanisms that establish these tonotopic maps are not known. Eph receptor tyrosine kinases and their ligands, the ephrins, have a demonstrated role in establishing topographic projections elsewhere in the brain, including the visual pathway. Here, we have examined the function of these proteins in the formation of auditory frequency maps. In birds, the first central auditory nucleus, n. magnocellularis (NM), projects tonotopically to n. laminaris (NL) on both sides of the brain. We previously showed that the Eph receptor EphA4 is expressed in a tonotopic gradient in the chick NL, with higher frequency regions showing greater expression than lower frequency regions. Here we misexpressed EphA4 in the developing auditory brainstem from embryonic day 2 (E2) through E10, when NM axons make synaptic contact with NL. We then evaluated topography along the frequency axis using both anterograde and retrograde labeling in both the ipsilateral and contralateral NM‐NL pathways. We found that after misexpression, NM regions project to a significantly broader proportion of NL than in control embryos, and that both the ipsilateral map and the contralateral map show this increased divergence. These results support a role for EphA4 in establishing tonotopic projections in the auditory system, and further suggest a general role for Eph family proteins in establishing topographic maps in the nervous system. © 2007 Wiley Periodicals, Inc. Develop Neurobiol, 2007

[1]  Shaowen Bao,et al.  Disruption of primary auditory cortex by synchronous auditory inputs during a critical period , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[2]  D. O'Leary,et al.  Molecular gradients and development of retinotopic maps. , 2005, Annual review of neuroscience.

[3]  D. O'Leary,et al.  Graded and lamina-specific distributions of ligands of EphB receptor tyrosine kinases in the developing retinotectal system. , 1997, Developmental biology.

[4]  Karina S. Cramer,et al.  Eph proteins and the assembly of auditory circuits , 2005, Hearing Research.

[5]  E. Rubel,et al.  Avian superior olivary nucleus provides divergent inhibitory input to parallel auditory pathways , 2005, The Journal of comparative neurology.

[6]  E. Pasquale,et al.  EphA receptors and ephrin-A ligands exhibit highly regulated spatial and temporal expression patterns in the developing olfactory system. , 2002, Brain research. Developmental brain research.

[7]  J G Flanagan,et al.  Malformation of the Functional Organization of Somatosensory Cortex in Adult Ephrin-A5 Knock-Out Mice Revealed by In Vivo Functional Imaging , 2000, The Journal of Neuroscience.

[8]  E. Rubel,et al.  Embryogenesis of arborization pattern and topography of individual axons in N. Laminaris of the chicken brain stem , 1986, The Journal of comparative neurology.

[9]  K. Kullander,et al.  Mechanisms and functions of eph and ephrin signalling , 2002, Nature Reviews Molecular Cell Biology.

[10]  E. Friauf,et al.  Development of auditory brainstem circuitry , 1999, Cell and Tissue Research.

[11]  Katsushige Sato,et al.  Development of functional synaptic connections in the auditory system visualized with optical recording: afferent-evoked activity is present from early stages. , 2006, Journal of neurophysiology.

[12]  I. Black,et al.  Regulation of topographic projection in the brain: Elf-1 in the hippocamposeptal system. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[13]  Development of auditory brainstem circuitry. Activity-dependent and activity-independent processes. , 1999, Cell and tissue research.

[14]  U. Drescher,et al.  Topographic targeting and pathfinding errors of retinal axons following overexpression of ephrinA ligands on retinal ganglion cell axons. , 1999, Developmental biology.

[15]  G. Lemke,et al.  Retinotectal mapping: new insights from molecular genetics. , 2005, Annual review of cell and developmental biology.

[16]  John G Flanagan,et al.  Ephrin‐A2 and ‐A5 influence patterning of normal and novel retinal projections to the thalamus: Conserved mapping mechanisms in visual and auditory thalamic targets , 2005, The Journal of comparative neurology.

[17]  E. Rubel,et al.  Developmental regulation of ephA4 expression in the chick auditory brainstem , 2000, The Journal of comparative neurology.

[18]  E. Rubel,et al.  Frequency-specific projections of individual neurons in chick brainstem auditory nuclei , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[19]  A. Flenniken,et al.  Eph Receptors and Ligands Comprise Two Major Specificity Subclasses and Are Reciprocally Compartmentalized during Embryogenesis , 1996, Neuron.

[20]  Russell L. Snyder,et al.  Topography of spiral ganglion projections to cochlear nucleus during postnatal development in cats , 1997, The Journal of comparative neurology.

[21]  John G. Flanagan,et al.  Genetic Analysis of Ephrin-A2 and Ephrin-A5 Shows Their Requirement in Multiple Aspects of Retinocollicular Mapping , 2000, Neuron.

[22]  Bernd Fritzsch,et al.  Auditory system development: primary auditory neurons and their targets. , 2002, Annual review of neuroscience.

[23]  T. Pawson,et al.  Nuk Controls Pathfinding of Commissural Axons in the Mammalian Central Nervous System , 1996, Cell.

[24]  K. Kullander,et al.  Area Specificity and Topography of Thalamocortical Projections Are Controlled by ephrin/Eph Genes , 2003, Neuron.

[25]  B. Ryals,et al.  Patterns of hair cell loss in chick basilar papilla after intense auditory stimulation. Exposure duration and survival time. , 1982, Acta oto-laryngologica.

[26]  M. Stryker,et al.  Ephrin-As Guide the Formation of Functional Maps in the Visual Cortex , 2005, Neuron.

[27]  G. Feng,et al.  Roles for Ephrins in Positionally Selective Synaptogenesis between Motor Neurons and Muscle Fibers , 2000, Neuron.

[28]  J. Rinzel,et al.  The role of dendrites in auditory coincidence detection , 1998, Nature.

[29]  B. Ryals,et al.  Patterns of hair cell loss in chick basilar papilla after intense auditory stimulation. Frequency organization. , 1982, Acta oto-laryngologica.

[30]  Uwe Drescher,et al.  Ephrin-As as receptors in topographic projections , 2002, Trends in Neurosciences.

[31]  A. Huberman,et al.  Ephrin-As mediate targeting of eye-specific projections to the lateral geniculate nucleus , 2005, Nature Neuroscience.

[32]  D. O'Leary,et al.  EphB Forward Signaling Controls Directional Branch Extension and Arborization Required for Dorsal-Ventral Retinotopic Mapping , 2002, Neuron.

[33]  E. Rubel,et al.  Ontogeny of tonotopic organization of brain stem auditory nuclei in the chicken: Implications for development of the place principle , 1985, The Journal of comparative neurology.

[34]  T. McLaughlin,et al.  Topographic-Specific Axon Branching Controlled by Ephrin-As Is the Critical Event in Retinotectal Map Development , 2001, The Journal of Neuroscience.

[35]  John G Flanagan,et al.  Topographically Specific Effects of ELF-1 on Retinal Axon Guidance In Vitro and Retinal Axon Mapping In Vivo , 1996, Cell.

[36]  Paul A Yates,et al.  Bifunctional action of ephrin-B1 as a repellent and attractant to control bidirectional branch extension in dorsal-ventral retinotopic mapping , 2003, Development.

[37]  G. Gates,et al.  The development of auditory evoked responses in the cochlea and cochlear nuclei of the chick. , 1973, Brain research.

[38]  A. Kania,et al.  Topographic Motor Projections in the Limb Imposed by LIM Homeodomain Protein Regulation of Ephrin-A:EphA Interactions , 2003, Neuron.

[39]  John G Flanagan,et al.  Retinal Axon Response to Ephrin-As Shows a Graded, Concentration-Dependent Transition from Growth Promotion to Inhibition , 2004, Neuron.

[40]  Greg Lemke,et al.  A relative signalling model for the formation of a topographic neural map , 2004, Nature.

[41]  E. Rubel,et al.  Tonotopic gradients of Eph family proteins in the chick nucleus laminaris during synaptogenesis. , 2004, Journal of neurobiology.

[42]  S. Fraser,et al.  Embryonic origins of auditory brain-stem nuclei in the chick hindbrain. , 2000, Developmental biology.

[43]  G. Yancopoulos,et al.  Mistargeting hippocampal axons by expression of a truncated Eph receptor , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[44]  E. Rubel,et al.  Organization and development of brain stem auditory nuclei of the chicken: Tonotopic organization of N. magnocellularis and N. laminaris , 1975, The Journal of comparative neurology.

[45]  D. Cerretti,et al.  EphB2 regulates axonal growth at the midline in the developing auditory brainstem. , 2006, Developmental biology.

[46]  D. Sanes,et al.  Activity‐dependent Refinement of Inhibitory Connections , 1993, The European journal of neuroscience.

[47]  S. Schneider-Maunoury,et al.  Targeting of the EphA4 tyrosine kinase receptor affects dorsal/ventral pathfinding of limb motor axons. , 2000, Development.

[48]  John G Flanagan,et al.  Complementary gradients in expression and binding of ELF-1 and Mek4 in development of the topographic retinotectal projection map , 1995, Cell.

[49]  C. Holt,et al.  Topographic Mapping in Dorsoventral Axis of the Xenopus Retinotectal System Depends on Signaling through Ephrin-B Ligands , 2002, Neuron.

[50]  K. Kandler,et al.  Elimination and strengthening of glycinergic/GABAergic connections during tonotopic map formation , 2003, Nature Neuroscience.

[51]  Elena B. Pasquale,et al.  Developmental cell biology: Eph receptor signalling casts a wide net on cell behaviour , 2005, Nature Reviews Molecular Cell Biology.

[52]  John G Flanagan,et al.  Loss-of-Function Analysis of EphA Receptors in Retinotectal Mapping , 2004, The Journal of Neuroscience.

[53]  E. Rubel,et al.  Expression of EphB receptors and EphrinB ligands in the developing chick auditory brainstem , 2002, The Journal of comparative neurology.

[54]  T. Pawson,et al.  Bidirectional signalling through the EPH-family receptor Nuk and its transmembrane ligands , 1996, Nature.

[55]  E. Debski,et al.  Activity-dependent mapping in the retinotectal projection , 2002, Current Opinion in Neurobiology.

[56]  Chen Li,et al.  Repelling class discrimination: ephrin-A5 binds to and activates EphB2 receptor signaling , 2004, Nature Neuroscience.

[57]  E. Pasquale,et al.  Tyrosine Phosphorylation of Transmembrane Ligands for Eph Receptors , 1997, Science.

[58]  Paul A Yates,et al.  Topographic Mapping from the Retina to the Midbrain Is Controlled by Relative but Not Absolute Levels of EphA Receptor Signaling , 2000, Cell.

[59]  Scott E. Fraser,et al.  Effects of brain-derived neurotrophic factor on optic axon branching and remodelling in vivo , 1995, Nature.

[60]  E. Pasquale Developmental cell biology: Eph receptor signalling casts a wide net on cell behaviour , 2005, Nature Reviews Molecular Cell Biology.

[61]  O. Marín,et al.  Differential expression of Eph receptors and ephrins correlates with the formation of topographic projections in primary and secondary visual circuits of the embryonic chick forebrain. , 2001, Developmental biology.

[62]  J. T. Hackett,et al.  Organization and development of brain stem auditory nuclei in the chick: Ontogeny of postsynaptic responses , 1982, The Journal of comparative neurology.

[63]  Ron D. Frostig,et al.  A mapping label required for normal scale of body representation in the cortex , 2000, Nature Neuroscience.

[64]  M. Sur,et al.  Enhanced Plasticity of Retinothalamic Projections in an Ephrin-A2/A5 Double Mutant , 2001, The Journal of Neuroscience.

[65]  K. Cramer,et al.  Differential expression of Eph receptors and ephrins in the cochlear ganglion and eighth cranial nerve of the chick embryo , 2005, The Journal of comparative neurology.

[66]  E. Rubel,et al.  EphA4 signaling promotes axon segregation in the developing auditory system. , 2004, Developmental biology.

[67]  Richard Axel,et al.  Axonal Ephrin-As and Odorant Receptors Coordinate Determination of the Olfactory Sensory Map , 2003, Cell.

[68]  J. Flanagan,et al.  Detection of Ligands in Regions Anatomically Connected to Neurons Expressing the Eph Receptor Bsk: Potential Roles in Neuron–Target Interaction , 1996, The Journal of Neuroscience.

[69]  D. Cerretti,et al.  Ephrin-dependent growth and pruning of hippocampal axons. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[70]  E. Rubel,et al.  Ontogenetic expression of trk neurotrophin receptors in the chick auditory system , 1999, The Journal of comparative neurology.

[71]  John G Flanagan,et al.  Ephrin-As and neural activity are required for eye-specific patterning during retinogeniculate mapping , 2005, Nature Neuroscience.

[72]  E. Rubel,et al.  Timing and topography of nucleus magnocellularis innervation by the cochlear ganglion , 2003, The Journal of comparative neurology.

[73]  C. Holt,et al.  New views on retinal axon development: a navigation guide. , 2004, The International journal of developmental biology.

[74]  Russell L. Snyder,et al.  Postnatal refinement of auditory nerve projections to the cochlear nucleus in cats , 2002, The Journal of comparative neurology.

[75]  E. Pasquale,et al.  Ephrin-A5 Exerts Positive or Inhibitory Effects on Distinct Subsets of EphA4-Positive Motor Neurons , 2004, The Journal of Neuroscience.