Disruption of Critical Period Plasticity in a Mouse Model of Neurofibromatosis Type 1

Autor: Nawal Zabouri, M. Hadi Saiepour, J. Alexander Heimel, Juliette E. Cheyne, Mariska van Lier, Christiaan N. Levelt, Yi Qin, Koen Kole, Christian Lohmann, Thomas Blok, Emma Ruimschotel
Přispěvatelé: Functional Genomics, Amsterdam Neuroscience - Cellular & Molecular Mechanisms, Center for Neurogenomics and Cognitive Research, Molecular and Cellular Neurobiology, Netherlands Institute for Neuroscience (NIN)
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Zdroj: van Lier, M, Saiepour, M H, Kole, K, Cheyne, J E, Zabouri, N, Blok, T, Qin, Y, Ruimschotel, E, Heimel, J A, Lohmann, C & Levelt, C N 2020, ' Disruption of Critical Period Plasticity in a Mouse Model of Neurofibromatosis Type 1 ', The Journal of neuroscience : the official journal of the Society for Neuroscience, vol. 40, no. 28, pp. 5495-5509 . https://doi.org/10.1523/JNEUROSCI.2235-19.2020
The Journal of neuroscience : the official journal of the Society for Neuroscience, 40(28), 5495-5509. Society for Neuroscience
The Journal of neuroscience : the official journal of the Society for Neuroscience, 40, 5495-5509. Society for Neuroscience
J Neurosci
ISSN: 0270-6474
DOI: 10.1523/JNEUROSCI.2235-19.2020
Popis: Neurofibromatosis type 1 (NF1) is a common monogenic neurodevelopmental disorder associated with physical and cognitive problems. The cognitive issues are thought to arise from increased release of the neurotransmitter γ-amino butyric acid (GABA). Modulating the signaling pathways causing increased GABA release in a mouse model of NF1 reverts deficits in hippocampal learning. However, clinical trials based on these approaches have so far been unsuccessful. We therefore used a combination of slice electrophysiology, in vivo two-photon calcium imaging and optical imaging of intrinsic signal in a mouse model of NF1 to investigate whether cortical development is affected in NF1, possibly causing lifelong consequences that cannot be rescued by reducing inhibition later in life. We find that in NF1 mice of both sexes, inhibition increases strongly during the development of the visual cortex and remains high. While this increase in cortical inhibition does not affect spontaneous cortical activity patterns during early cortical development, the critical period for ocular dominance plasticity is shortened in NF1 mice due to its early closure but unaltered onset. Notably, after environmental enrichment, differences in inhibitory innervation and ocular dominance plasticity between NF1 mice and wild-type litter mates disappear. These results provide the first evidence for critical period dysregulation in NF1 and suggest that treatments aimed at normalizing levels of inhibition will need to start at early stages of development.Significance:Neurofibromatosis type 1 is associated with cognitive problems for which no treatment is currently available. This study shows that in a mouse model of Neurofibromatosis type 1, cortical inhibition is increased during development and critical period regulation is disturbed. Rearing the mice in an environment that stimulates cognitive function overcomes these deficits. These results uncover critical period dysregulation as a novel mechanism in the pathogenesis of Neurofibromatosis type 1. This suggests that targeting the affected signaling pathways in Neurofibromatosis type 1 for the treatment of cognitive disabilities may have to start at a much younger age than has so far been tested in clinical trials.
Databáze: OpenAIRE
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