Dual-channel circuit mapping reveals sensorimotor convergence in the primary motor cortex

J Neurosci. 2015 Mar 11;35(10):4418-26. doi: 10.1523/JNEUROSCI.3741-14.2015.

Abstract

Cortical cells integrate synaptic input from multiple sources, but how these different inputs are distributed across individual neurons is largely unknown. Differences in input might account for diverse responses in neighboring neurons during behavior. We present a strategy for comparing the strengths of multiple types of input onto the same neuron. We developed methods for independent dual-channel photostimulation of synaptic inputs using ChR2 together with ReaChR, a red-shifted channelrhodopsin. We used dual-channel photostimulation to probe convergence of sensory information in the mouse primary motor cortex. Input from somatosensory cortex and thalamus converges in individual neurons. Similarly, inputs from distinct somatotopic regions of the somatosensory cortex are integrated at the level of single motor cortex neurons. We next developed a ReaChR transgenic mouse under the control of both Flp- and Cre-recombinases that is an effective tool for circuit mapping. Our approach to dual-channel photostimulation enables quantitative comparison of the strengths of multiple pathways across all length scales of the brain.

Keywords: ReaChR; circuit mapping; dual-channel stimulation; motor cortex; optogenetics; somatosensory cortex.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Brain Mapping*
  • Channelrhodopsins
  • Excitatory Amino Acid Antagonists / pharmacology
  • Excitatory Postsynaptic Potentials / drug effects
  • Excitatory Postsynaptic Potentials / physiology
  • Female
  • In Vitro Techniques
  • Light
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Male
  • Mice
  • Motor Cortex / cytology*
  • Nerve Net / physiology*
  • Neurons / physiology*
  • Piperazines / pharmacology
  • Quinoxalines / pharmacology
  • Sodium Channel Blockers / pharmacology
  • Somatosensory Cortex / physiology*
  • Tetrodotoxin / pharmacology
  • Transduction, Genetic

Substances

  • Channelrhodopsins
  • Excitatory Amino Acid Antagonists
  • Luminescent Proteins
  • Piperazines
  • Quinoxalines
  • Sodium Channel Blockers
  • 2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline
  • Tetrodotoxin
  • 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid