Filleting and Immunostaining of Larvae to Visualize Drosophila Dendritic Arborization Neuron Dendrite Arbors

Cold Spring Harb Protoc. 2024 Dec 2;2024(12):pdb.prot108148. doi: 10.1101/pdb.prot108148.

Abstract

Nervous system formation involves the specification of neuron identity, followed by precise circuit construction; this includes controlling the pattern and connectivity of the dendrite arbor. Drosophila dendritic arborization (da) neurons are a powerful experimental model for studying dendrite arbor differentiation mechanisms. da neuron dendrite arbors elaborate in two dimensions in the body wall, making it easy to visualize them with high resolution. Immunostaining is a conventional method to examine arbor pattern and the subcellular distribution of proteins. In addition, images acquired from immunostaining protocols can amplify weaker signals from fluorescent transgenic proteins and be used to quantify protein expression levels. This protocol describes a broadly applicable dissection, fixation, and immunostaining approach in Drosophila larvae.

MeSH terms

  • Animals
  • Dendrites* / metabolism
  • Dendrites* / physiology
  • Dissection / methods
  • Drosophila* / cytology
  • Larva* / cytology
  • Neurons / cytology
  • Neurons / metabolism
  • Staining and Labeling / methods