Rapid Preparation of Living Drosophila Pupal Macrophages for Ex Vivo Imaging

Tua Karling, Helen Weavers*

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapter in a book

Abstract

The fruit fly Drosophila is a well-established invertebrate model that enables in vivo imaging of innate immune cell (e.g., macrophage) migration and signaling at high spatiotemporal resolution within the intact, living animal. While optimized methods already exist to enable flow cytometry-based macrophage isolation from Drosophila at various stages of development, there remains a need for more rapid and gentle methods to isolate living macrophages for downstream ex vivo applications. Here, we describe techniques for rapid and direct isolation of living macrophages from mature Drosophila pupae and their downstream ex vivo preparation for live imaging and immunostaining. This strategy enables straightforward access to physiologically relevant innate immune cells, both circulating and tissue-resident populations, for subsequent imaging of signal transduction.

Original languageEnglish
Title of host publicationImaging Cell Signalling
PublisherHumana Press
Pages1-10
Number of pages10
ISBN (Electronic)9781071638347
ISBN (Print)9781071638330
DOIs
Publication statusPublished - 7 May 2024

Publication series

NameMethods in Molecular Biology
Volume2800
ISSN (Print)1064-3745
ISSN (Electronic)1940-6029

Bibliographical note

Publisher Copyright:
© The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature 2024.

Keywords

  • Animals
  • Pupa/cytology
  • Macrophages/cytology
  • Drosophila
  • Cell Separation/methods
  • Flow Cytometry/methods
  • Drosophila melanogaster/cytology

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