Single synaptic inputs drive high-precision action potentials in parvalbumin expressing GABA-ergic cortical neurons in vivo

Nat Commun. 2018 Apr 18;9(1):1540. doi: 10.1038/s41467-018-03995-2.

Abstract

A defining feature of cortical layer 2/3 excitatory neurons is their sparse activity, often firing in singlets of action potentials. Local inhibitory neurons are thought to play a major role in regulating sparseness, but which cell types are recruited by single excitatory synaptic inputs is unknown. Using multiple, targeted, in vivo whole-cell recordings, we show that single uEPSPs have little effect on the firing rates of excitatory neurons and somatostatin-expressing GABA-ergic inhibitory neurons but evoke precisely timed action potentials in parvalbumin-expressing inhibitory neurons. Despite a uEPSP decay time of 7.8 ms, the evoked action potentials were almost completely restricted to the uEPSP rising phase (~0.5 ms). Evoked parvalbumin-expressing neuron action potentials go on to inhibit the local excitatory network, thus providing a pathway for single spike evoked disynaptic inhibition which may enforce sparse and precisely timed cortical signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology*
  • Animals
  • Cerebral Cortex / metabolism*
  • GABAergic Neurons / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Neural Inhibition / physiology
  • Parvalbumins / chemistry*
  • Patch-Clamp Techniques
  • Photons
  • Software
  • Somatostatin / chemistry
  • Synapses / physiology*
  • gamma-Aminobutyric Acid / pharmacology

Substances

  • Parvalbumins
  • Somatostatin
  • gamma-Aminobutyric Acid