Stabilization of Gaze during Early Xenopus Development by Swimming-Related Utricular Signals.

François M. Lambert, Julien Bacqué-Cazenave, Anne Le Seach, Jessica Arama, Gilles Courtand, Michele Tagliabue, Selim Eskiizmirliler, Hans Straka, Mathieu Beraneck
Current Biology. 2020-01-01; :
DOI: 10.1016/j.cub.2019.12.047

Lire sur PubMed

Lambert FM(1), Bacqué-Cazenave J(2), Le Seach A(3), Arama J(3), Courtand G(2),Tagliabue M(3), Eskiizmirliler S(3), Straka H(4), Beraneck M(5).

Author information:
(1)INCIA, CNRS UMR 5287, Université de Bordeaux, F-33076 Bordeaux, France. Electronic address: .
(2)INCIA, CNRS UMR 5287, Université de Bordeaux, F-33076 Bordeaux, France.
(3)Integrative Neuroscience and Cognition Center, CNRS UMR 8002, Université de Paris, F-75270 Paris, France.
(4)Department Biology II, Ludwig-Maximilians-University Munich, Grosshaderner Str. 2, 82152 Planegg, Germany.
(5)Integrative Neuroscience and Cognition Center, CNRS UMR 8002, Université de Paris, F-75270 Paris, France. Electronic address:

Locomotor maturation requires concurrent gaze stabilization improvement for maintaining visual acuity (1, 2). The capacity to stabilize gaze, in particular in small aquatic vertebrates where coordinated locomotor activity appears very early, is determined by assembly and functional maturation of inner ear structures and associated sensory-motor circuitries (3-7). Whereas utriculo-ocular reflexes become functional immediately after hatching (8, 9), semicircular canal-dependent vestibulo-ocular reflexes (VORs) appear later (10). Thus, small semicircular canals are unable to detect swimming-related head oscillations, despite the fact that corresponding acceleration components are well-suited to trigger an angular VOR (11). This leaves the utricle as the sole
vestibular origin for swimming-related compensatory eye movements (12, 13). We report a remarkable ontogenetic plasticity of swimming-related head kinematics and vestibular end organ recruitment in Xenopus tadpoles with beneficial consequences for gaze-stabilization. Swimming of older larvae generates sinusoidal head undulations with small, similar curvature angles on the left and right side that optimally activate horizontal semicircular canals. Young larvae swimming causes left-right head undulations with narrow curvatures and strong, bilaterally dissimilar centripetal acceleration components well suited to activate utricular hair cells and to substitute the absent semicircular canal function at this stage. The capacity of utricular signals to supplant semicircular canal function was confirmed by recordings of eye movements and extraocular motoneurons during off-center rotations in control and semicircular canal-deficient tadpoles. Strong alternating curvature angles and thus linear acceleration profiles during swimming in young larvae therefore represents a technically elegant solution to compensate for the incapacity of small semicircular canals to detect angular acceleration components.

Auteurs Bordeaux Neurocampus