Developmental regulation of glial cell phagocytic function during Drosophila embryogenesis

Boris Shklyar, Yael Sellman, Jeny Shklover, Ketty Mishnaevski, Flonia Levy-Adam, Estee Kurant

Research output: Contribution to journalArticlepeer-review


The proper removal of superfluous neurons through apoptosis and subsequent phagocytosis is essential for normal development of the central nervous system (CNS). During Drosophila embryogenesis, a large number of apoptotic neurons are efficiently engulfed and degraded by phagocytic glia. Here we demonstrate that glial proficiency to phagocytose relies on expression of phagocytic receptors for apoptotic cells, SIMU and DRPR. Moreover, we reveal that the phagocytic ability of embryonic glia is established as part of a developmental program responsible for glial cell fate determination and is not triggered by apoptosis per se. Explicitly, we provide evidence for a critical role of the major regulators of glial identity, gcm and repo, in controlling glial phagocytic function through regulation of SIMU and DRPR specific expression. Taken together, our study uncovers molecular mechanisms essential for establishment of embryonic glia as primary phagocytes during CNS development.

Original languageEnglish
Pages (from-to)255-269
Number of pages15
JournalDevelopmental Biology
Issue number2
StatePublished - 2014
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2014 Elsevier Inc.


  • Apoptosis
  • Development
  • Drosophila
  • Glia
  • Phagocytosis
  • SIMU

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology
  • Developmental Biology


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