Epidermal cells are the primary phagocytes in the fragmentation and clearance of degenerating dendrites in Drosophila

Neuron. 2014 Feb 5;81(3):544-560. doi: 10.1016/j.neuron.2013.11.021. Epub 2014 Jan 9.

Abstract

During developmental remodeling, neurites destined for pruning often degenerate on-site. Physical injury also induces degeneration of neurites distal to the injury site. Prompt clearance of degenerating neurites is important for maintaining tissue homeostasis and preventing inflammatory responses. Here we show that in both dendrite pruning and dendrite injury of Drosophila sensory neurons, epidermal cells rather than hemocytes are the primary phagocytes in clearing degenerating dendrites. Epidermal cells act via Draper-mediated recognition to facilitate dendrite degeneration and to engulf and degrade degenerating dendrites. Using multiple dendritic membrane markers to trace phagocytosis, we show that two members of the CD36 family, croquemort (crq) and debris buster (dsb), act at distinct stages of phagosome maturation for dendrite clearance. Our finding reveals the physiological importance of coordination between neurons and their surrounding epidermis, for both dendrite fragmentation and clearance.

Publication types

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

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • CD36 Antigens / metabolism
  • Dendrites / metabolism*
  • Dendrites / ultrastructure
  • Drosophila
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism
  • Epidermal Cells*
  • Epithelial Cells / physiology*
  • Gene Expression Regulation, Developmental / genetics
  • Larva
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Microscopy, Confocal
  • Microscopy, Electron, Transmission
  • Mutation / genetics
  • Nerve Degeneration / pathology
  • Nerve Degeneration / physiopathology*
  • Phagocytosis / physiology*
  • Pupa
  • RNA Interference / physiology
  • Receptors, Scavenger / genetics
  • Receptors, Scavenger / metabolism
  • Sensory Receptor Cells / cytology*
  • Time Factors

Substances

  • CD36 Antigens
  • Drosophila Proteins
  • Luminescent Proteins
  • Receptors, Scavenger
  • crq protein, Drosophila