The laminar organization of the Drosophila ellipsoid body is semaphorin-dependent and prevents the formation of ectopic synaptic connections

Elife. 2017 Jun 20:6:e25328. doi: 10.7554/eLife.25328.

Abstract

The ellipsoid body (EB) in the Drosophila brain is a central complex (CX) substructure that harbors circumferentially laminated ring (R) neuron axons and mediates multifaceted sensory integration and motor coordination functions. However, what regulates R axon lamination and how lamination affects R neuron function remain unknown. We show here that the EB is sequentially innervated by small-field and large-field neurons and that early developing EB neurons play an important regulatory role in EB laminae formation. The transmembrane proteins semaphorin-1a (Sema-1a) and plexin A function together to regulate R axon lamination. R neurons recruit both GABA and GABA-A receptors to their axon terminals in the EB, and optogenetic stimulation coupled with electrophysiological recordings show that Sema-1a-dependent R axon lamination is required for preventing the spread of synaptic inhibition between adjacent EB lamina. These results provide direct evidence that EB lamination is critical for local pre-synaptic inhibitory circuit organization.

Keywords: D. melanogaster; central complex; developmental biology; ellipsoid body; neural lamination; neuroscience; semaphorin; stem cells.

Publication types

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

MeSH terms

  • Animals
  • Brain / embryology
  • Drosophila / embryology*
  • Drosophila Proteins / metabolism
  • Electrophysiological Phenomena
  • Nerve Tissue Proteins / metabolism
  • Neural Pathways / embryology*
  • Optogenetics
  • Organogenesis
  • Presynaptic Terminals / physiology
  • Receptors, Cell Surface / metabolism
  • Semaphorins / metabolism*

Substances

  • Drosophila Proteins
  • Nerve Tissue Proteins
  • Receptors, Cell Surface
  • Semaphorins
  • plexA protein, Drosophila
  • semaphorin 1a, Drosophila