Differential expression of Eph receptors and ephrins in the cochlear ganglion and eighth cranial nerve of the chick embryo

✍ Scribed by Shazia A. Siddiqui; Karina S. Cramer

• Publisher: John Wiley and Sons
• Year: 2005
• Tongue: English
• Weight: 757 KB
• Volume: 482
• Category: Article
• ISSN: 0021-9967
• DOI: 10.1002/cne.20396

✦ Synopsis

Abstract

The cochleovestibular ganglion of the chick differentiates at early embryonic stages as VIIIth nerve axons enter the brainstem. The tonotopic organization of the auditory portion of the VIIIth nerve can be discerned at the time axons initially reach their brainstem targets. The mechanisms underlying this early organization are not known. Eph receptor tyrosine kinases and their ligands, the ephrins, have a demonstrated role in guiding axons to topographically appropriate locations in other areas of the nervous system. In order to begin to test whether Eph proteins have a similar role in the auditory system, we investigated the tonotopic expression of several Eph receptors and ephrins in the VIIIth nerve during embryonic ages corresponding to the initial innervation of the auditory brainstem. Expression patterns of EphA4, EphB2, EphB5, ephrin‐A2, and ephrin‐B1 were evaluated immunohistochemically at embryonic days 4 through 10. Protein expression was observed in the cochlear ganglion and VIIIth nerve axons at these ages. EphB5, ephrin‐A2, and ephrin‐B1 were expressed throughout the nerve. EphA4 and EphB2 had complementary expression patterns within the nerve, with EphA4 expression higher in the dorsolateral part of the nerve and EphB2 expression higher in the ventromedial part of the nerve. These regions may correspond to auditory and vestibular components, respectively. Moreover, EphA4 expression was higher toward the low‐frequency region of both the centrally and peripherally projecting branches of cochlear ganglion cells. Regional variation of Eph protein expression may influence the target selection and topography of developing VIIIth nerve projections. J. Comp. Neurol. 482:309–319, 2005. © 2005 Wiley‐Liss, Inc.