Actin cytoskeleton reorganization of the apoptotic nurse cells during the late developmental stages of oogenesis in Dacus oleae

Cell Motil Cytoskeleton. 2001 Mar;48(3):224-33. doi: 10.1002/1097-0169(200103)48:3<224::AID-CM1011>3.0.CO;2-O.

Abstract

In the present study, we demonstrate the actin cytoskeleton reorganization during nurse cells apoptosis of the olive fruit fly Dacus oleae. At the developmental stage 9A of oogenesis, the actin microfilaments are assembled in numerous ring canals and subcortically support all the nurse cells, as is shown by phalloidin-FITC staining. During the following stages, 9B and 10A, this structural pattern remains the same. The developmental stage 10B is characterized by actin microfilament rearrangement and formation of actin cables that are symmetrically organized around the nurse cell nuclei. At stage 11, when the dumping process begins, these actin cables seem to retain each nurse cell nucleus in the cell center, away from blocking the ring canals. The early stage 12 is characterized by an asynchronous nurse cell nuclear chromatin condensation, while at late stage 12 the actin cables become very thick, as adjacent ones overlap one another and traverse the disorganized apoptotic nurse cell nuclei that already have fragmented DNA, as is demonstrated by acridine orange staining and TUNEL assay. Finally, during stage 13, the apoptotic nuclear remnants are phagocytosed by the neighboring follicle cells. The data presented herein compared to previous reported results in Drosophila [Nezis et al., 2000: Eur J Cell Biol 79:610-620], demonstrate that actin cytoskeleton reorganization during nurse cell apoptosis is a developmentally regulated physiological mechanism, phylogenetically conserved in higher Dipteran.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acridine Orange / pharmacology
  • Actins / metabolism*
  • Actins / physiology*
  • Animals
  • Apoptosis*
  • Cell Nucleus / metabolism
  • Cytoskeleton / metabolism*
  • Cytoskeleton / ultrastructure
  • DNA Fragmentation
  • Diptera / physiology*
  • Fluorescent Dyes / pharmacology
  • In Situ Nick-End Labeling
  • Microscopy, Confocal
  • Microscopy, Electron
  • Oocytes / metabolism
  • Oocytes / ultrastructure
  • Oogenesis / physiology*
  • Phagocytosis
  • Phalloidine / metabolism
  • Time Factors

Substances

  • Actins
  • Fluorescent Dyes
  • Phalloidine
  • Acridine Orange