The Claustrum Supports Resilience to Distraction

Curr Biol. 2018 Sep 10;28(17):2752-2762.e7. doi: 10.1016/j.cub.2018.06.068. Epub 2018 Aug 16.

Abstract

A barrage of information constantly assaults our senses, of which only a fraction is relevant at any given point in time. However, the neural circuitry supporting the suppression of irrelevant sensory distractors is not completely understood. The claustrum, a circuit hub with vast cortical connectivity, is an intriguing brain structure, whose restrictive anatomy, thin and elongated, has precluded functional investigation. Here, we describe the use of Egr2-CRE mice to access genetically defined claustral neurons. Utilizing conditional viruses for anterograde axonal labeling and retrograde trans-synaptic tracing, we validated this transgenic model for accessing the claustrum and extended the known repertoire of claustral input/output connectivity. Addressing the function of the claustrum, we inactivated CLEgr2+ neurons, chronically as well as acutely, in mice performing an automated two-alternative forced-choice behavioral task. Strikingly, inhibition of CLEgr2+ neurons did not significantly impact task performance under varying delay times and cue durations, but revealed a selective role for the claustrum in supporting performance in the presence of an irrelevant auditory distractor. Further investigation of behavior, in the naturalistic maternal pup-retrieval task, replicated the result of sensitization to an auditory distractor following inhibition of CLEgr2+ neurons. Initiating investigation into the underlying mechanism, we found that activation of CLEgr2+ neurons modulated cortical sensory processing, suppressing tone representation in the auditory cortex. This functional study, utilizing selective genetic access, implicates the claustrum in supporting resilience to distraction, a fundamental aspect of attention.

Keywords: attention; auditory cortex; chemogenetics; claustrum; cortical gain; distraction; fiber photometry; optogenetics; sensory selection; transgenic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Attention / physiology*
  • Basal Ganglia / physiology*
  • Behavior, Animal / physiology
  • Early Growth Response Protein 2 / genetics
  • Early Growth Response Protein 2 / metabolism
  • Female
  • Gene Knock-In Techniques
  • Integrases / genetics
  • Integrases / metabolism
  • Mice
  • Mice, Inbred Strains
  • Neural Pathways / physiology
  • Neurons / physiology*

Substances

  • Early Growth Response Protein 2
  • Egr2 protein, mouse
  • Cre recombinase
  • Integrases