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Higgs, N. F.

Publications and source records attributed to Higgs, N. F..

3 recordsLinked to original sources

NMDA receptor activation drives early synapse formation in vivo

The rules governing neural circuit formation in mammalian central nervous systems are poorly understood. NMDA receptors are involved in synaptic plasticity mechanisms in mature neurons, but their contribution to circuit formation and dendritic maturation remains controversial. Using pharmacological and genetic interventions to disrupt NMDA receptor signaling in hippocampal CA1 pyramidal neurons in vitro and in vivo, we identify an early critical window for a synapse-specific function in wiring Schaffer collateral connections and dendritic arborization. Through in vivo imaging, we show that NMDA receptors are frequently activated during early development and elicit minute-long calcium transients, which immediately precede the emergence of filopodia. These results demonstrate that NMDA receptors drive synapto- and dendritogenesis during development, challenging the view that these processes are primarily mediated by molecular cues.

neuroscience↗

Miro1-dependent Mitochondrial Dynamics in Parvalbumin Interneurons

The spatiotemporal distribution of mitochondria is crucial for precise ATP provision and calcium buffering required to support neuronal signaling. Fast-spiking GABAergic interneurons expressing parvalbumin (PV) have a high mitochondrial content reflecting their large energy utilization. The importance for correct trafficking and precise mitochondrial positioning remains poorly elucidated in inhibitory neurons. Miro1 is a Ca2+-sensing adaptor protein that links mitochondria to the trafficking apparatus, for their microtubule-dependent transport along axons and dendrites, in order to meet the metabolic and Ca2+-buffering requirements of the cell. Here, we explore the role of Miro1 in parvalbumin interneurons and how changes in mitochondrial trafficking could alter brain network activity. By employing live and fixed imaging, we found that the impairments in Miro1-directed trafficking in PV+ interneurons altered their mitochondrial distribution and axonal arborization. These changes were accompanied by an increase in the ex vivo hippocampal {gamma}-oscillation (30 - 80 Hz) frequency and promoted anxiolysis. Our findings show that precise regulation of mitochondrial dynamics in PV+ interneurons is crucial for proper neuronal signaling and network synchronization.

neuroscience↗

Correct CYFIP1 dosage is essential for synaptic inhibition and the excitatory/inhibitory balance.

Altered excitatory/inhibitory balance is implicated in neuropsychiatric disorders but the genetic aetiology of this is still poorly understood. Copy number variations in CYFIP1 are associated with autism, schizophrenia and intellectual disability but the role of CYFIP1 in regulating synaptic inhibition or excitatory/inhibitory balance remains unclear. We show, CYFIP1, and its paralogue CYFIP2, are enriched at inhibitory postsynaptic sites. While upregulation of CYFIP1 or CYFIP2 increased excitatory synapse number and the frequency of miniature excitatory postsynaptic currents (mEPSCs), it had the opposite effect at inhibitory synapses, decreasing their size and the amplitude of miniature inhibitory postsynaptic currents (mIPSCs). Contrary to CYFIP1 upregulation, its loss in vivo, upon conditional knockout in neocortical principal cells, increased expression of postsynaptic GABAA receptor {beta}2/3-subunits and neuroligin 3 and enhanced synaptic inhibition. Thus, CYFIP1 dosage can bi-directionally impact inhibitory synaptic structure and function, potentially leading to altered excitatory/inhibitory balance and circuit dysfunction in CYFIP1-associated neurodevelopmental disorders.

neuroscience↗