It is suggested that early, transient Kv7-dependent CA1 dysfunction in FXS drives early, transient Kv7-dependent CA1 dysfunction in AIS development and highlights how alterations in AIS development can have profound functional impacts.
Abstract
Fragile X syndrome (FXS) is the leading monogenetic cause of intellectual disability and autism, yet how basic hippocampal circuit properties evolve across development for this condition remains unclear. Here, we studied CA1 pyramidal neurons in male Fmr1 knockout rats at postnatal day (P)12–15 and 6–10 weeks using ex vivo electrophysiology, pharmacology, imaging and biochemistry. P12–15 knockout neurons showed impaired sustained firing, progressive action potential broadening and enhanced activity-dependent synaptic vesicle replenishment. These defects recovered by 6–10 weeks. These phenotypes were linked to Kv7 channel dysfunction, as Kv7 activation altered action potential dynamics and neurotransmission in WT but not Fmr1 KO neurons. Rather than directly altering Kv7 channel function, Fmr1 knockout altered axon initial segment (AIS) development such that Kv7 became functionally inert. These findings suggest that this drives early, transient Kv7-dependent CA1 dysfunction in FXS and highlight how alterations in AIS development can have profound functional impacts.
It is concluded that CA1 PCs hyperexcitability from Frm1 KO mice was detectable at late postnatal development (P21-28), but not earlier (P8-15), and was due to a shifting of action potential voltage threshold to more hyperpolarized values.
M. A. Luque, L. Dufresne, B. Torres et al.· Neuroscience· 0 citations
It is shown that a pathogenic variant of the G protein subunit Gβ1 impairs activation of neuronal G-protein-coupled inwardly rectifying potassium (GIRK) channels by inhibitory synaptic GABAB receptors, which leads to increased dendritic excitability and longer duration dendritic calcium spikes in mouse hippocampal neur...
Sam Gritz, Anshul Voleti, Matthew S. Scarnati et al.· bioRxiv· 0 citations
It is found that Fmr1-/y rats displayed an age-dependent FC phenotype, with increased connectivity within the retrosplenial cortex (RSC) at 4 weeks but reduced connectivity within the RSC and distributed brain networks by adulthood compared with wild-type controls, which suggests FC abnormalities emerge over developmen...
Jing-Jing Ye, Joanna A. B. Surl, A. McKechanie et al.· bioRxiv· 0 citations
Functional analysis of neuronal activity reveals delayed synaptic maturation in loss-of-function mutations and insights into how KIF1A mutations with distinct molecular-level impacts lead to significant downstream synaptic deficits in human neurons.
Jayne Aiken, Carris Borland, Nicolas Marotta et al.· Journal of Cell Biology· 0 citations
It is shown that oligodendroglial Cit-k loss and the resulting hypomyelination are sufficient to produce long-lasting neurological and behavioral impairments independently of primary neuronal defects.
Martino Bonato, F. Marchiotto, Maryam Khastkhodaei Ardakani et al.· bioRxiv· 0 citations
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder traditionally characterized by motor neuron degeneration, but emerging evidence indicates sensory system involvement. Despite reports of sensory abnormalities in some patients, the molecular and functional alterations in dorsal root ganglio...
Akira Nishiura, S. Seki, Takuhiro Kobayashi et al.· bioRxiv· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.