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Ephrin-A5/EphA4 signalling controls specific afferent targeting to cochlear hair cells

机译:Ephrin-A5 / EphA4信号传导控制对耳蜗毛细胞的特定传入靶定

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摘要

Hearing requires an optimal afferent innervation of sensory hair cells by spiral ganglion neurons in the cochlea. Here we report that complementary expression of ephrin-A5 in hair cells and EphA4 receptor among spiral ganglion neuron populations controls the targeting of type I and type II afferent fibres to inner and outer hair cells, respectively. In the absence of ephrin-A5 or EphA4 forward signalling, a subset of type I projections aberrantly overshoot the inner hair cell layer and invade the outer hair cell area. Lack of type I afferent synapses impairs neurotransmission from inner hair cells to the auditory nerve. By contrast, radial shift of type I projections coincides with a gain of presynaptic ribbons that could enhance the afferent signalling from outer hair cells. Ephexin-1 , cofilin and myosin light chain kinase act downstream of EphA4 to induce type I spiral ganglion neuron growth cone collapse. Our findings constitute the first identification of an Eph/ephrin-mediated mutual repulsion mechanism responsible for specific sorting of auditory projections in the cochlea.
机译:听力需要通过耳蜗中的螺旋神经节神经元对感觉毛细胞进行最佳传入神经支配。在这里我们报告螺旋神经节神经元人口之间的毛细胞和EphA4受体中的ephrin-A5互补表达控制分别将I型和II型传入纤维靶向内,外毛细胞。在缺乏ephrin-A5或EphA4前向信号的情况下,I型突起的一个子集异常地超过了内部毛细胞层并侵入了外部毛细胞区域。 I型传入突触的缺乏会损害从内部毛细胞到听神经的神经传递。相比之下,I型突起的径向移位与突触前带的增加相吻合,这可以增强来自外部毛细胞的传入信号。 Ephexin-1,cofilin和肌球蛋白轻链激酶在EphA4的下游起作用,诱导I型螺旋神经节神经元生长锥塌陷。我们的发现构成了对以弗/ ephrin介导的相互排斥机制的首次鉴定,该机制负责耳蜗中听觉投射的特定排序。

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