Experimental analysis identifies discrete critical periods affecting sensorimotor function in mice, suggesting task-specific pathways.
Somatosensory circuits in early life must maintain stable, task-selective pathways while behavioural repertoires undergo rapid change. How such circuits construct these behaviours under evolving functional demands has remained unclear. Here we show that sensorimotor behaviours are shaped through sequential, experience-dependent critical periods rather than a single global window of plasticity. Using transient perturbations of somatosensory input across postnatal development in mice, we identify three discrete life stages that exert lasting effects on adult behaviour. Perturbation during postnatal days 8-12 selectively increases adult sensitivity to dynamic touch. The same manipulation during days 13-17 produces persistent deficits in motor coordination. Perturbation during days 18-22 instead results in lifelong impairments in skilled locomotion. These findings reveal that somatosensory circuits undergo multiple phases of refinement, each aligned with the changing functional needs of the developing organism. This framework of sequential, task-specific critical periods offers a new model for building lifelong sensorimotor function.
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Andreoli et al. (2025) studied this question.
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