Behavioral and electromyographic characterization of mice lacking EphA4 receptors

被引:71
作者
Akay, Turgay [1 ]
Acharya, Hernish J.
Fouad, Karim
Pearson, Keir G.
机构
[1] Univ Alberta, Dept Physiol, Edmonton, AB T6G 2H7, Canada
[2] Univ Alberta, Fac Rehabil Med, Edmonton, AB T6G 2H7, Canada
关键词
D O I
10.1152/jn.00174.2006
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
EphA4 receptors play an important role in axon guidance during development. Disrupting the expression of these receptors in mice has been shown to modify neuronal connections in the spinal cord and results in the production of a characteristic hopping gait. The EphA4-null mouse has been used in numerous investigations aimed at establishing mechanisms responsible for patterning motor activity during walking. However, there have been no detailed behavioral or electrophysiological studies on adult EphA4-null mice. We used high-speed video recordings to determine the coordination of leg movements during locomotion in adult EphA4-null mice. Our data show that the hopping movements of the hind legs are not always associated with synchronous movements of forelegs. The coupling between the forelegs is weak, resulting in changes in their phase relationship from step to step. The synchronous coordination of the hind legs can switch to an alternating pattern for a short period of time during recovery from isoflurane anesthesia. Comparison of the kinematics of hind leg movements in EphA4-null mice and wild-type animals shows that besides the synchronous coordination in EphA4-null mice, the swing durations and the swing amplitude are shorter. Electromyographic recordings from a knee extensor muscle show double bursting in the EphA4-null animals but single bursts in wild types. This double burst changes to single-burst activity during swimming and when hind legs are stepping in alternation. These observations suggest an influence of sensory feedback in shaping the pattern of muscle activity during locomotion in the mutant animals. Our data give the first detailed description of the locomotor behavior of an adult mouse with genetically manipulated spinal networks.
引用
收藏
页码:642 / 651
页数:10
相关论文
共 33 条
[1]
AKAY T, 2005, SOC NEUR ABSTR
[2]
Locomotor-like activity generated by the neonatal mouse spinal cord [J].
Bonnot, A ;
Whelan, PJ ;
Mentis, GZ ;
O'Donovan, MJ .
BRAIN RESEARCH REVIEWS, 2002, 40 (1-3) :141-151
[3]
Organization of rhythmic motor patterns in the lumbosacral spinal cord of neonate mouse [J].
Bonnot, A ;
Morin, D ;
Viala, D .
NEURONAL MECHANISMS FOR GENERATING LOCOMOTOR ACTIVITY, 1998, 860 :432-435
[4]
EphA4 defines a class of excitatory locomotor-related interneurons [J].
Butt, SJB ;
Lundfald, L ;
Kiehn, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (39) :14098-14103
[5]
Gait analysis in the mouse [J].
Clarke, KA ;
Still, J .
PHYSIOLOGY & BEHAVIOR, 1999, 66 (05) :723-729
[6]
FUNCTIONAL-PROPERTIES OF SPINAL INTERNEURONS ACTIVATED BY MUSCULAR FREE NERVE-ENDINGS AND THEIR POTENTIAL CONTRIBUTIONS TO THE CLASP-KNIFE REFLEX [J].
CLELAND, CL ;
RYMER, WZ .
JOURNAL OF NEUROPHYSIOLOGY, 1993, 69 (04) :1181-1191
[7]
EphA4 (Sek1) receptor tyrosine kinase is required for the development of the corticospinal tract [J].
Dottori, M ;
Hartley, L ;
Galea, M ;
Paxinos, G ;
Polizzotto, M ;
Kilpatrick, T ;
Bartlett, PF ;
Murphy, M ;
Köntgen, F ;
Boyd, AW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13248-13253
[8]
Load-regulating mechanisms in gait and posture: Comparative aspects [J].
Duysens, J ;
Clarac, F ;
Cruse, H .
PHYSIOLOGICAL REVIEWS, 2000, 80 (01) :83-133
[9]
Progression from extrinsic to intrinsic signaling in cell fate specification: A view from the nervous system [J].
Edlund, T ;
Jessell, TM .
CELL, 1999, 96 (02) :211-224
[10]
Regulation of EphA4 kinase activity is required for a subset of axon guidance decisions suggesting a key role for receptor clustering in Eph function [J].
Egea, J ;
Nissen, UV ;
Dufour, A ;
Sahin, M ;
Greer, P ;
Kullander, K ;
Mrsic-Flogel, TD ;
Greenberg, ME ;
Kiehn, O ;
Vanderhaeghen, P ;
Klein, R .
NEURON, 2005, 47 (04) :515-528