Abdul-Latif Mariam L, Salazar Jesus A Ayala, Marshak Sonya, Dinh Minhan L, Cramer Karina S
Division of Neonatology, Department of Pediatrics, University of California, Irvine, 101 The City Drive, Orange, CA, 92868-3298, USA.
Department of Neurobiology and Behavior, University of California, Irvine, 2205 McGaugh Hall, Irvine, CA, 92697-4550, USA.
Neural Dev. 2015 Dec 15;10:27. doi: 10.1186/s13064-015-0054-6.
In the auditory brainstem, ventral cochlear nucleus (VCN) axons project to the contralateral, but not ipsilateral, medial nucleus of trapezoid body (MNTB), terminating in the calyx of Held. Dorsal VCN neurons, representing high frequencies, synapse with medial MNTB neurons, while low frequency-coding ventral VCN neurons synapse with lateral MNTB neurons, reflecting tonotopic organization. The mechanisms that ensure strictly contralateral targeting and topographic ordering are incompletely understood. Here we examined the roles of ephrin-A signaling in both types of targeting.
Ephrin-A2 and ephrin-A5 are expressed in VCN cells during late embryonic and early postnatal development. At these ages ephrin-A2 is expressed in axons surrounding MNTB and ephrin-A5 is expressed in MNTB principal neurons. Ephrin-A2/A5 double knockout mice displayed axon targeting errors in which VCN axons project to MNTB on both sides of the brainstem, where they terminate in calyceal endings. Ephrin-A2 and ephrin-A5 single knockout mice showed a similar phenotype. In contrast to effects on contralateral targeting, ephrin-A2/A5 double knockout mice showed no defects in formation of tonotopically ordered projections from VCN to MNTB.
These findings demonstrate that distinct mechanisms regulate targeting of VCN axons to the contralateral MNTB and targeting to appropriate tonotopic locations. Ephrin-A signaling plays a similar role to ephrin-B signaling in the VCN-MNTB pathway, where both classes normally prevent formation of calyceal projections to ipsilateral MNTB. These classes may rely in part on common signaling pathways.
在听觉脑干中,蜗腹侧核(VCN)轴突投射至对侧而非同侧的斜方体内侧核(MNTB),并终止于 Held 壶腹。代表高频的背侧 VCN 神经元与内侧 MNTB 神经元形成突触,而编码低频的腹侧 VCN 神经元与外侧 MNTB 神经元形成突触,这反映了音频拓扑组织。确保严格对侧靶向和拓扑排序的机制尚未完全了解。在此,我们研究了 Ephrin-A 信号在这两种靶向类型中的作用。
Ephrin-A2 和 Ephrin-A5 在胚胎后期和出生后早期发育阶段的 VCN 细胞中表达。在这些年龄段,Ephrin-A2 在围绕 MNTB 的轴突中表达,而 Ephrin-A5 在 MNTB 主神经元中表达。Ephrin-A2/A5 双敲除小鼠表现出轴突靶向错误,其中 VCN 轴突投射至脑干两侧的 MNTB,并在壶腹末梢终止。Ephrin-A2 和 Ephrin-A5 单敲除小鼠表现出类似的表型。与对侧靶向的影响相反,Ephrin-A2/A5 双敲除小鼠在从 VCN 到 MNTB 的音频拓扑有序投射形成方面没有缺陷。
这些发现表明,不同的机制调节 VCN 轴突向对侧 MNTB 的靶向以及向适当音频拓扑位置的靶向。Ephrin-A 信号在 VCN-MNTB 通路中发挥与 Ephrin-B 信号类似的作用,在该通路中,这两类信号通常都能防止形成向同侧 MNTB 的壶腹投射。这些类别可能部分依赖于共同的信号通路。