Nature neuroscience · 2018
Inhibitory circuit gating of auditory critical-period plasticity.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Takesian Anne E, Bogart Luke J, Lichtman Jeff W, Hensch Takao K
Аннотация
Cortical sensory maps are remodeled during early life to adapt to the surrounding environment. Both sensory and contextual signals are important for induction of this plasticity, but how these signals converge to sculpt developing thalamocortical circuits remains largely unknown. Here we show that layer 1 (L1) of primary auditory cortex (A1) is a key hub where neuromodulatory and topographically organized thalamic inputs meet to tune the cortical layers below. Inhibitory interneurons in L1 send narrowly descending projections to differentially modulate thalamic drive to pyramidal and parvalbumin-expressing (PV) cells in L4, creating brief windows of intracolumnar activation. Silencing of L1 (but not VIP-expressing) cells abolishes map plasticity during the tonotopic critical period. Developmental transitions in nicotinic acetylcholine receptor (nAChR) sensitivity in these cells caused by Lynx1 protein can be overridden to extend critical-period closure. Notably, thalamocortical maps in L1 are themselves stable, and serve as a scaffold for cortical plasticity throughout life.
Предметные рубрики MeSH
AnimalsAuditory CortexBicucullineBiguanidesEvoked Potentials, Auditory, Brain StemExcitatory Postsynaptic PotentialsFemaleInterneuronsMaleMiceMice, Inbred C57BLMice, TransgenicNeuronal PlasticityNicotineNicotinic AgonistsOtoacoustic Emissions, SpontaneousParvalbuminsSensory GatingSerotonin Receptor AgonistsVasoactive Intestinal Peptide