4.7 Article

A subpopulation of cortical VIP-expressing interneurons with highly dynamic spines

Journal

COMMUNICATIONS BIOLOGY
Volume 5, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s42003-022-03278-z

Keywords

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Funding

  1. Swiss National Science Foundation [31003A_153448, 31003A_173125, CRSII3_154453]
  2. Marie Skodowska-Curie Actions [895465]
  3. Initial Training Networks Projects Marie Curie Actions, NPLAST
  4. International Foundation for Research in paraplegia (Chair Alain Rossier)
  5. Swiss National Science Foundation (SNF) [31003A_153448, CRSII3_154453, 31003A_173125] Funding Source: Swiss National Science Foundation (SNF)
  6. Marie Curie Actions (MSCA) [895465] Funding Source: Marie Curie Actions (MSCA)

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This study identifies a subset of superficial multipolar inhibitory interneurons expressing VIP with high dynamics, located in layer 1 of the cortex, and exhibiting the electrophysiological characteristics of bursting cells. The structural plasticity of these neurons is distinct from that of excitatory neurons.
Structural synaptic plasticity may underlie experience and learning-dependent changes in cortical circuits. In contrast to excitatory pyramidal neurons, insight into the structural plasticity of inhibitory neurons remains limited. Interneurons are divided into various subclasses, each with specialized functions in cortical circuits. Further knowledge of subclass-specific structural plasticity of interneurons is crucial to gaining a complete mechanistic understanding of their contribution to cortical plasticity overall. Here, we describe a subpopulation of superficial cortical multipolar interneurons expressing vasoactive intestinal peptide (VIP) with high spine densities on their dendrites located in layer (L) 1, and with the electrophysiological characteristics of bursting cells. Using longitudinal imaging in vivo, we found that the majority of the spines are highly dynamic, displaying lifetimes considerably shorter than that of spines on pyramidal neurons. Using correlative light and electron microscopy, we confirmed that these VIP spines are sites of excitatory synaptic contacts, and are morphologically distinct from other spines in L1. Advanced light and electron microscopy identify a subset of cortical multipolar vasoactive intestinal peptide interneurons with high spine dynamics and characteristics that are greatly different from pyramidal neurons.

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