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 language | English |
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Title of host publication | Imaging Cell Signalling |
Publisher | Humana Press |
Pages | 1-10 |
Number of pages | 10 |
ISBN (Electronic) | 9781071638347 |
ISBN (Print) | 9781071638330 |
DOIs | |
Publication status | Published - 7 May 2024 |
Publication series
Name | Methods in Molecular Biology |
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Volume | 2800 |
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