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Updated: Feb 13, 2026

Imaging Cell Shape Change in Living Drosophila Embryos
Published on: March 30, 2011
Analysis of Cell Shape and Cell Migration of Drosophila Macrophages In Vivo
Marike Rüder1, Benedikt M Nagel1, Sven Bogdan2
1Institut für Physiologie und Pathophysiologie, Abteilung Molekulare Zellphysiologie, Phillips-Universität Marburg, Marburg, Germany.
Abstract:
The most abundant immune cells in Drosophila are macrophage-like plasmatocytes that fulfill central roles in morphogenesis, immune and tissue damage response. The various genetic tools available in Drosophila together with high-resolution and live-imaging microscopy techniques make Drosophila macrophages an excellent model system that combines many advantages of cultured cells with in vivo genetics. Here, we describe the isolation and staining of macrophages from larvae for ex vivo structured illumination microscopy (SIM), the preparation of white prepupae for in vivo 2D random cell migration analysis, and the preparation of pupae (18 h after puparium formation, APF) for in vivo 3D directed cell migration analysis upon wounding using spinning disk microscopy.
Insights
Drosophila plasmatocytes, essential immune cells, are studied using advanced microscopy. This research details methods for analyzing their migration in vivo and ex vivo, aiding developmental and immune response studies.
Area of Science:
- * Developmental Biology
- * Immunology
- * Cell Biology
Background:
- * Macrophage-like plasmatocytes are the primary immune cells in Drosophila.
- * These cells play crucial roles in development, immunity, and tissue repair.
- * Drosophila offers a powerful model for studying macrophage behavior due to its genetic tools and imaging capabilities.
Purpose of the Study:
- * To detail methodologies for analyzing Drosophila macrophage migration.
- * To enable ex vivo and in vivo studies of plasmatocyte behavior.
- * To facilitate research into morphogenesis, immune response, and tissue damage repair.
Main Methods:
- * Isolation and staining of larval macrophages for ex vivo structured illumination microscopy (SIM).
- * Preparation of white prepupae for in vivo 2D random cell migration analysis.
- * Preparation of pupae for in vivo 3D directed cell migration analysis using spinning disk microscopy.
Main Results:
- * Established protocols for high-resolution imaging of Drosophila macrophages.
- * Demonstrated techniques for analyzing both random and directed cell migration in vivo.
- * Provided a framework for investigating plasmatocyte dynamics in various biological contexts.
Conclusions:
- * Drosophila macrophages are amenable to detailed study using advanced microscopy techniques.
- * The described methods support in vivo and ex vivo analysis of cell migration.
- * This work enhances the utility of Drosophila as a model for cell-based biological research.
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