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1.
J Comp Neurol ; 529(16): 3633-3654, 2021 11.
Article in English | MEDLINE | ID: mdl-34235739

ABSTRACT

Tonotopy is a prominent feature of the vertebrate auditory system and forms the basis for sound discrimination, but the molecular mechanism that underlies its formation remains largely elusive. Ephrin/Eph signaling is known to play important roles in axon guidance during topographic mapping in other sensory systems, so we investigated its possible role in the establishment of tonotopy in the mouse cochlear nucleus. We found that ephrin-A3 molecules are differentially expressed along the tonotopic axis in the cochlear nucleus during innervation. Ephrin-A3 forward signaling is sufficient to repel auditory nerve fibers in a developmental stage-dependent manner. In mice lacking ephrin-A3, the tonotopic map is degraded and isofrequency bands of neuronal activation upon pure tone exposure become imprecise in the anteroventral cochlear nucleus. Ephrin-A3 mutant mice also exhibit a delayed second wave in auditory brainstem responses upon sound stimuli and impaired detection of sound frequency changes. Our findings establish an essential role for ephrin-A3 in forming precise tonotopy in the auditory brainstem to ensure accurate sound discrimination.


Subject(s)
Brain Stem/physiology , Ephrin-A3/genetics , Ephrin-A3/physiology , Evoked Potentials, Auditory, Brain Stem/physiology , Hearing/physiology , Acoustic Stimulation , Animals , Audiometry, Pure-Tone , Brain Mapping , Cochlear Nucleus/physiology , Evoked Potentials, Auditory, Brain Stem/genetics , Female , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Mutation , Pitch Discrimination
2.
Proc Natl Acad Sci U S A ; 106(30): 12524-9, 2009 Jul 28.
Article in English | MEDLINE | ID: mdl-19592509

ABSTRACT

Increasing evidence indicates the importance of neuron-glia communication for synaptic function, but the mechanisms involved are not fully understood. We reported that the EphA4 receptor tyrosine kinase is in dendritic spines of pyramidal neurons of the adult hippocampus and regulates spine morphology. We now show that the ephrin-A3 ligand, which is located in the perisynaptic processes of astrocytes, is essential for maintaining EphA4 activation and normal spine morphology in vivo. Ephrin-A3-knockout mice have spine irregularities similar to those observed in EphA4-knockout mice. Remarkably, loss of ephrin-A3 or EphA4 increases the expression of glial glutamate transporters. Consistent with this, glutamate transport is elevated in ephrin-A3-null hippocampal slices whereas Eph-dependent stimulation of ephrin-A3 signaling inhibits glutamate transport. Furthermore, some forms of hippocampus-dependent learning are impaired in the ephrin-A3-knockout mice. Our results suggest that the interaction between neuronal EphA4 and glial ephrin-A3 bidirectionally controls synapse morphology and glial glutamate transport, ultimately regulating hippocampal function.


Subject(s)
Dendritic Spines/physiology , Ephrin-A3/physiology , Glutamates/metabolism , Neuroglia/metabolism , Amino Acid Transport System X-AG/metabolism , Analysis of Variance , Animals , Astrocytes/cytology , Astrocytes/metabolism , Biological Transport , Dendritic Spines/metabolism , Ephrin-A3/genetics , Ephrin-A3/metabolism , Hippocampus/cytology , Hippocampus/metabolism , Immunoblotting , Immunoprecipitation , Maze Learning/physiology , Memory/physiology , Mice , Mice, Knockout , Microscopy, Confocal , Microscopy, Fluorescence , Motor Activity/physiology , Phosphorylation , Pyramidal Cells/cytology , Pyramidal Cells/metabolism , Receptor, EphA4/genetics , Receptor, EphA4/metabolism , Receptor, EphA4/physiology
3.
J Dermatol Sci ; 52(3): 178-85, 2008 Dec.
Article in English | MEDLINE | ID: mdl-18640011

ABSTRACT

BACKGROUND: Ephrins are cell-membrane-bound ligands for Eph receptor tyrosine kinases (Eph). Although ephrins are known to regulate a variety of developmental processes, little is known of their role in hair development. Previously, we studied the gene expression of dermal papilla cells from androgenetic alopecia and found that ephrin-A3 was significantly down-regulated. OBJECTIVE: To characterize the expression of ephrin-A3 in the hair cycle and evaluate the effect of ephrin-A3 on hair growth. METHODS: We investigated gene expression and protein expression of each ephrin-As and EphAs in the skin of neonatal mice through the first and second hair cycle using quantitative PCR and immunohistochemical analysis, respectively. We also injected ephrin-A3 protein into the skin of neonatal mice and demonstrated the effect of ephrin-A3 on hair follicle development. RESULTS: Expression of ephrin-A3 revealed a rapid increase at the beginning of the anagen phase, a peak during the mid-anagen, and a rapid fading during the telogen phase. In addition, we found ephrin-A3 protein was expressed in the developing hair follicles with a characteristic spatiotemporal localization. Furthermore, injection of ephrin-A3 into the skin of neonatal mice markedly accelerated the differentiation process of hair follicles. In addition, injection of ephrin-A3 unexpectedly increased the number of hair follicles. CONCLUSION: These findings demonstrated that ephrin-A3 not only accelerates anagen development but also increases the density of hair follicles, and also suggested that an ephrin-A-EphA signal pathway is closely involved in hair follicle development.


Subject(s)
Ephrin-A3/physiology , Hair Follicle/growth & development , Animals , Animals, Newborn , Endothelial Cells/chemistry , Ephrin-A3/analysis , Ephrin-A3/genetics , Female , Mice , Mice, Inbred C3H , Mice, Inbred C57BL
4.
Neuron ; 48(4): 577-89, 2005 Nov 23.
Article in English | MEDLINE | ID: mdl-16301175

ABSTRACT

Ephrin-As and their receptors, EphAs, are expressed in the developing cortex where they may act to organize thalamic inputs. Here, we map the visual cortex (V1) in mice deficient for ephrin-A2, -A3, and -A5 functionally, using intrinsic signal optical imaging and microelectrode recording, and structurally, by anatomical tracing of thalamocortical projections. V1 is shifted medially, rotated, and compressed and its internal organization is degraded. Expressing ephrin-A5 ectopically by in utero electroporation in the lateral cortex shifts the map of V1 medially, and expression within V1 disrupts its internal organization. These findings indicate that interactions between gradients of EphA/ephrin-A in the cortex guide map formation, but that factors other than redundant ephrin-As are responsible for the remnant map. Together with earlier work on the retinogeniculate map, the current findings show that the same molecular interactions may operate at successive stages of the visual pathway to organize maps.


Subject(s)
Brain Mapping , Ephrin-A2/physiology , Ephrin-A3/physiology , Ephrin-A5/physiology , Visual Cortex/embryology , Visual Cortex/physiology , Aging/metabolism , Aging/physiology , Animals , Animals, Newborn , Embryonic Development , Ephrin-A2/deficiency , Ephrin-A2/metabolism , Ephrin-A3/deficiency , Ephrin-A3/metabolism , Ephrin-A5/deficiency , Ephrin-A5/metabolism , Ligands , Mice , Mice, Knockout , Retina/physiology , Synaptic Transmission/physiology , Thalamus/embryology , Thalamus/growth & development , Thalamus/physiology , Visual Cortex/growth & development
5.
Nat Neurosci ; 8(8): 1022-7, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16025107

ABSTRACT

In mammals, retinal ganglion cell (RGC) projections initially intermingle and then segregate into a stereotyped pattern of eye-specific layers in the dorsal lateral geniculate nucleus (dLGN). Here we found that in mice deficient for ephrin-A2, ephrin-A3 and ephrin-A5, eye-specific inputs segregated but the shape and location of eye-specific layers were profoundly disrupted. In contrast, mice that lacked correlated retinal activity did not segregate eye-specific inputs. Inhibition of correlated neural activity in ephrin mutants led to overlapping retinal projections that were located in inappropriate regions of the dLGN. Thus, ephrin-As and neural activity act together to control patterning of eye-specific retinogeniculate layers.


Subject(s)
Body Patterning/physiology , Ephrin-A2/physiology , Ephrin-A3/physiology , Ephrin-A5/physiology , Geniculate Bodies/physiology , Retinal Ganglion Cells/physiology , Synaptic Transmission/physiology , Animals , Brain Mapping , Ephrin-A2/deficiency , Ephrin-A3/deficiency , Ephrin-A5/deficiency , Mice , Mice, Knockout , Receptor, EphA2/deficiency , Receptor, EphA3/deficiency , Receptor, EphA5/deficiency , Visual Pathways/physiology
6.
Nat Neurosci ; 8(8): 1013-21, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16025110

ABSTRACT

Axon guidance cues contributing to the development of eye-specific visual projections to the lateral geniculate nucleus (LGN) have not previously been identified. Here we show that gradients of ephrin-As and their receptors (EphAs) direct retinal ganglion cell (RGC) axons from the two eyes into their stereotyped pattern of layers in the LGN. Overexpression of EphAs in ferret RGCs using in vivo electroporation induced axons from both eyes to misproject within the LGN. The effects of EphA overexpression were competition-dependent and restricted to the early postnatal period. These findings represent the first demonstration of eye-specific pathfinding mediated by axon guidance cues and, taken with other reports, indicate that ephrin-As can mediate several mapping functions within individual target structures.


Subject(s)
Ephrin-A3/physiology , Ephrin-A5/physiology , Geniculate Bodies/physiology , Receptors, Eph Family/physiology , Retinal Ganglion Cells/physiology , Synaptic Transmission , Aging/metabolism , Animals , Animals, Newborn , Axons/physiology , Electroporation , Ephrin-A3/metabolism , Ephrin-A5/metabolism , Female , Ferrets , Green Fluorescent Proteins , Luminescent Agents , Male , Receptor, EphA3/physiology , Receptor, EphA5/physiology , Visual Pathways/metabolism
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