Sonic hedgehog expression in corticofugal projection neurons directs cortical microcircuit formation

Neuron. 2012 Mar 22;73(6):1116-26. doi: 10.1016/j.neuron.2012.02.009. Epub 2012 Mar 21.

Abstract

The precise connectivity of inputs and outputs is critical for cerebral cortex function; however, the cellular mechanisms that establish these connections are poorly understood. Here, we show that the secreted molecule Sonic Hedgehog (Shh) is involved in synapse formation of a specific cortical circuit. Shh is expressed in layer V corticofugal projection neurons and the Shh receptor, Brother of CDO (Boc), is expressed in local and callosal projection neurons of layer II/III that synapse onto the subcortical projection neurons. Layer V neurons of mice lacking functional Shh exhibit decreased synapses. Conversely, the loss of functional Boc leads to a reduction in the strength of synaptic connections onto layer Vb, but not layer II/III, pyramidal neurons. These results demonstrate that Shh is expressed in postsynaptic target cells while Boc is expressed in a complementary population of presynaptic input neurons, and they function to guide the formation of cortical microcircuitry.

Publication types

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

MeSH terms

  • Age Factors
  • Animals
  • Animals, Newborn
  • Cerebral Cortex / cytology*
  • Cerebral Cortex / growth & development
  • Channelrhodopsins
  • Corpus Callosum / cytology
  • Corpus Callosum / growth & development
  • DNA-Binding Proteins / metabolism
  • Dendritic Spines / metabolism
  • Dendritic Spines / physiology
  • Electric Stimulation
  • Electroporation / methods
  • Fluorobenzenes / metabolism
  • Functional Laterality / genetics
  • Furans / metabolism
  • Gene Expression Regulation, Developmental / genetics
  • Gene Expression Regulation, Developmental / physiology*
  • Hedgehog Proteins / genetics
  • Hedgehog Proteins / metabolism*
  • Immunoglobulin G / genetics
  • Immunoglobulin G / metabolism
  • In Vitro Techniques
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Matrix Attachment Region Binding Proteins / metabolism
  • Membrane Potentials / genetics
  • Mice
  • Mice, Transgenic
  • Mutation / genetics
  • Nerve Net / cytology
  • Nerve Net / metabolism*
  • Neurons / metabolism*
  • Neurons / ultrastructure
  • Nuclear Proteins / metabolism
  • Patch-Clamp Techniques
  • Phosphopyruvate Hydratase / metabolism
  • Pyramidal Tracts / physiology*
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism
  • Repressor Proteins / metabolism
  • Silver Staining / methods
  • Stilbamidines / metabolism
  • Synapses / metabolism
  • Synapses / ultrastructure
  • Synaptophysin / genetics
  • Synaptophysin / metabolism
  • Transcription Factors / metabolism
  • Tumor Suppressor Proteins / metabolism
  • Ubiquitin-Protein Ligases
  • gamma-Aminobutyric Acid / metabolism

Substances

  • 2-hydroxy-4,4'-diamidinostilbene, methanesulfonate salt
  • 3,4-difluorobenzyloxy-5,5-dimethyl-4-(4-methylsulfonylphenyl)-(5H)-furan-2-one
  • Bcl11b protein, mouse
  • Boc protein, mouse
  • Channelrhodopsins
  • DNA-Binding Proteins
  • Fluorobenzenes
  • Furans
  • Hedgehog Proteins
  • Immunoglobulin G
  • Luminescent Proteins
  • Matrix Attachment Region Binding Proteins
  • Nuclear Proteins
  • RNA, Small Interfering
  • Receptors, Cell Surface
  • Repressor Proteins
  • SATB2 protein, mouse
  • Shh protein, mouse
  • Stilbamidines
  • Synaptophysin
  • Transcription Factors
  • Tumor Suppressor Proteins
  • gamma-Aminobutyric Acid
  • Trim27 protein, mouse
  • Ubiquitin-Protein Ligases
  • Phosphopyruvate Hydratase