Live cell tracking of macrophage efferocytosis during Drosophila embryo development in vivo

Author:

Raymond Michael H.123ORCID,Davidson Andrew J.4ORCID,Shen Yi5ORCID,Tudor Daniel R.6ORCID,Lucas Christopher D.4ORCID,Morioka Sho127ORCID,Perry Justin S. A.8,Krapivkina Julia9ORCID,Perrais David9ORCID,Schumacher Linus J.6ORCID,Campbell Robert E.510ORCID,Wood Will4ORCID,Ravichandran Kodi S.121112ORCID

Affiliation:

1. Center for Cell Clearance, University of Virginia, Charlottesville, VA, USA.

2. Department of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, VA, USA.

3. Neuroscience Graduate Program, University of Virginia, Charlottesville, VA, USA.

4. Centre for Inflammation Research, University of Edinburgh, Edinburgh BioQuarter, Edinburgh, UK.

5. Department of Chemistry, University of Alberta, Edmonton, Canada.

6. Centre for Regenerative Medicine, University of Edinburgh, Edinburgh BioQuarter, Edinburgh, UK.

7. Department of Medicine, Division of Nephrology and CIIR, University of Virginia, Charlottesville, VA, USA.

8. Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

9. University of Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience (IINS), UMR 5297, Bordeaux, France.

10. Department of Chemistry, School of Science, The University of Tokyo, Bunkyo-ku, Tokyo, 113-0033, Japan.

11. VIB/UGent Inflammation Research Centre, and Biomedical Molecular Biology, Ghent University, Belgium.

12. Division of Immunobiology, Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA.

Abstract

Apoptosis of cells and their subsequent removal through efferocytosis occurs in nearly all tissues during development, homeostasis, and disease. However, it has been difficult to track cell death and subsequent corpse removal in vivo. We developed a genetically encoded fluorescent reporter, CharON (Caspase and pH Activated Reporter, Fluorescence ON), that could track emerging apoptotic cells and their efferocytic clearance by phagocytes. Using Drosophila expressing CharON, we uncovered multiple qualitative and quantitative features of coordinated clearance of apoptotic corpses during embryonic development. When confronted with high rates of emerging apoptotic corpses, the macrophages displayed heterogeneity in engulfment behaviors, leading to some efferocytic macrophages carrying high corpse burden. Overburdened macrophages were compromised in clearing wound debris. These findings reveal known and unexpected features of apoptosis and macrophage efferocytosis in vivo.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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