Corticothalamic Spike Transfer via the L5B-POm Pathway in vivo

Cereb Cortex. 2016 Aug;26(8):3461-75. doi: 10.1093/cercor/bhw123. Epub 2016 May 12.

Abstract

The cortex connects to the thalamus via extensive corticothalamic (CT) pathways, but their function in vivo is not well understood. We investigated "top-down" signaling from cortex to thalamus via the cortical layer 5B (L5B) to posterior medial nucleus (POm) pathway in the whisker system of the anesthetized mouse. While L5B CT inputs to POm are extremely strong in vitro, ongoing activity of L5 neurons in vivo might tonically depress these inputs and thereby block CT spike transfer. We find robust transfer of spikes from the cortex to the thalamus, mediated by few L5B-POm synapses. However, the gain of this pathway is not constant but instead is controlled by global cortical Up and Down states. We characterized in vivo CT spike transfer by analyzing unitary PSPs and found that a minority of PSPs drove POm spikes when CT gain peaked at the beginning of Up states. CT gain declined sharply during Up states due to frequency-dependent adaptation, resulting in periodic high gain-low gain oscillations. We estimate that POm neurons receive few (2-3) active L5B inputs. Thus, the L5B-POm pathway strongly amplifies the output of a few L5B neurons and locks thalamic POm sub-and suprathreshold activity to cortical L5B spiking.

Keywords: POm; VGAT; adaptation; barrel cortex; corticothalamic feedback; layer 5; somatosensory system; thy-1.

MeSH terms

  • Action Potentials
  • Anesthesia
  • Animals
  • Computer Simulation
  • Excitatory Postsynaptic Potentials
  • GABA-A Receptor Agonists / pharmacology
  • Mice, Transgenic
  • Microelectrodes
  • Models, Neurological
  • Muscimol / pharmacology
  • Neural Pathways / cytology
  • Neural Pathways / physiology
  • Neuroanatomical Tract-Tracing Techniques
  • Neurons / cytology
  • Neurons / physiology*
  • Optogenetics
  • Somatosensory Cortex / cytology
  • Somatosensory Cortex / drug effects
  • Somatosensory Cortex / physiology*
  • Thalamus / cytology
  • Thalamus / physiology*
  • Vesicular Inhibitory Amino Acid Transport Proteins / genetics
  • Vesicular Inhibitory Amino Acid Transport Proteins / metabolism
  • Vibrissae / innervation
  • Vibrissae / physiology

Substances

  • GABA-A Receptor Agonists
  • Vesicular Inhibitory Amino Acid Transport Proteins
  • Viaat protein, mouse
  • Muscimol