Proceedings of the National Academy of Sciences · 2012 · 98 citations · 29 references
Life SciencesNeurobiologyNeuroscienceDevelopmental NeuroscienceMotor ControlNeurophysiologyFish LocomotionMotor SystemsNeural DevelopmentSpinal Cord CircuitsSpinal Cord PhysiologySpinal Motor CircuitsLocomotion In Larval FishLocomotor Rhythm GenerationNeural Circuitry Of LocomotionNeural Control Of LocomotionSpinal Cord Locomotor CircuitsSpinal InterneuronsSpinal Locomotor CircuitsSpinal Motor Circuit Function
Spinal cord circuits convert brain signals into coordinated locomotor rhythms via rhythm‑generating components, yet the molecular identity and necessity of excitatory interneurons in this process remain unclear. V2a interneurons are an intrinsic excitatory source essential for normal locomotor rhythm, as their selective ablation raises swimming thresholds, reduces burst frequency, and disrupts rostro‑caudal coordination, demonstrating their role in enabling locomotion.
Neural circuits in the spinal cord transform instructive signals from the brain into well-coordinated locomotor movements by virtue of rhythm-generating components. Although evidence suggests that excitatory interneurons are the essence of locomotor rhythm generation, their molecular identity and the assessment of their necessity have remained unclear. Here we show, using larval zebrafish, that V2a interneurons represent an intrinsic source of excitation necessary for the normal expression of the locomotor rhythm. Acute and selective ablation of these interneurons increases the threshold of induction of swimming activity, decreases the burst frequency, and alters the coordination of the rostro–caudal propagation of activity. Thus, our results argue that V2a interneurons represent a source of excitation that endows the spinal circuit with the capacity to generate locomotion.
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