Single-Cell mRNA Profiling Reveals Cell-Type-Specific Expression of Neurexin Isoforms

Neuron. 2015 Jul 15;87(2):326-40. doi: 10.1016/j.neuron.2015.06.028.

Abstract

Neurexins are considered central organizers of synapse architecture that are implicated in neuropsychiatric disorders. Expression of neurexins in hundreds of alternatively spliced isoforms suggested that individual neurons might exhibit a cell-type-specific neurexin expression pattern (a neurexin code). To test this hypothesis, we quantified the single-cell levels of neurexin isoforms and other trans-synaptic cell-adhesion molecules by microfluidics-based RT-PCR. We show that the neurexin repertoire displays pronounced cell-type specificity that is remarkably consistent within each type of neuron. Furthermore, we uncovered region-specific regulation of neurexin transcription and splice-site usage. Finally, we demonstrate that the transcriptional profiles of neurexins can be altered in an experience-dependent fashion by exposure to a drug of abuse. Our data provide evidence of cell-type-specific expression patterns of multiple neurexins at the single-cell level and suggest that expression of synaptic cell-adhesion molecules overlaps with other key features of cellular identity and diversity.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Brain / cytology*
  • Cholecystokinin / metabolism
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • HEK293 Cells
  • Humans
  • In Vitro Techniques
  • Mice, Inbred C57BL
  • Nerve Net / physiology
  • Neural Cell Adhesion Molecules / genetics
  • Neural Cell Adhesion Molecules / metabolism*
  • Neurons / classification*
  • Neurons / metabolism*
  • Parvalbumins / genetics
  • Parvalbumins / metabolism
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • RNA, Messenger / metabolism*
  • Receptors, Dopamine D2 / genetics
  • Receptors, Dopamine D2 / metabolism
  • Statistics, Nonparametric
  • Time Factors
  • Transcriptome
  • Transduction, Genetic

Substances

  • Neural Cell Adhesion Molecules
  • Parvalbumins
  • Protein Isoforms
  • RNA, Messenger
  • Receptors, Dopamine D2
  • Green Fluorescent Proteins
  • Cholecystokinin