Resident phagocytes promote non–cell-autonomous fragmentation of apoptotic cells

Phagocytosis of apoptotic cells maintains tissue homeostasis and regulates inflammation. A proposed facilitator of apoptotic cell clearance is the fragmentation of these cells into apoptotic bodies (ApoBDs) through cell-autonomous processes involving caspases and cytoskeletal rearrangement. Although this fragmentation process is considered a hallmark of apoptosis, its progression in tissue environments remains underexplored. Here, we examine the in vivo apoptotic dynamics of mouse thymocytes and pluripotent cells from zebrafish embryos. We show that the in vivo biogenesis of ApoBDs is independent of known cell-intrinsic regulators. Instead, fragmentation depends on actin-rich protrusions from neighboring resident phagocytes, which mechanically compress apoptotic cells to break them into smaller particles. Four-dimensional in vivo tracking of apoptotic cells reveals that both phagocyte-mediated fragmentation and phagocytosis are size sensitive, indicating that apoptotic size reduction mediated by phagocytes enhances their own clearance abilities. This non-cell-autonomous fragmentation ensures rapid apoptotic cell clearance, crucial for maintaining tissue homeostasis in physiological settings.

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Publication Details

Journal
Science Advances
Published
2025-12-17
DOI
https://doi.org/10.1126/sciadv.adz5264
Primary Topic
Phagocytosis and Immune Regulation
Type
article
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article

Resident phagocytes promote non–cell-autonomous fragmentation of apoptotic cells

Rochelle Tixeira, Michael F. Olson, Esteban Hoijman, Ivan K. H. Poon et al.
Science Advances
Phagocytosis and Immune Regulation
article

Resident phagocytes promote non–cell-autonomous fragmentation of apoptotic cells

Rochelle Tixeira, Michael F. Olson, Esteban Hoijman, Ivan K. H. Poon, Joan Roncero-Carol, Amy A. Baxter, Andrew J. Kueh, Gemma F. Ryan, Lanzhou Jiang, Dilara C. Ozkocak, Georgia K. Atkin‐Smith, Jascinta P. Santavanond, Amy L. Hodge, Daniel H.D. Gray, Marco J. Herold, Mark D. Hulett, Kelin Zhao, Irene Lozano-González
article en

Abstract

Phagocytosis of apoptotic cells maintains tissue homeostasis and regulates inflammation. A proposed facilitator of apoptotic cell clearance is the fragmentation of these cells into apoptotic bodies (ApoBDs) through cell-autonomous processes involving caspases and cytoskeletal rearrangement. Although this fragmentation process is considered a hallmark of apoptosis, its progression in tissue environments remains underexplored. Here, we examine the in vivo apoptotic dynamics of mouse thymocytes and pluripotent cells from zebrafish embryos. We show that the in vivo biogenesis of ApoBDs is independent of known cell-intrinsic regulators. Instead, fragmentation depends on actin-rich protrusions from neighboring resident phagocytes, which mechanically compress apoptotic cells to break them into smaller particles. Four-dimensional in vivo tracking of apoptotic cells reveals that both phagocyte-mediated fragmentation and phagocytosis are size sensitive, indicating that apoptotic size reduction mediated by phagocytes enhances their own clearance abilities. This non-cell-autonomous fragmentation ensures rapid apoptotic cell clearance, crucial for maintaining tissue homeostasis in physiological settings.

Science AdvancesVol. 11(51)
The University of Melbourne (AU), Walter and Eliza Hall Institute of Medical Research (AU), La Trobe University (AU), Ghent University (BE), Institut d'Investigació Biomédica de Bellvitge (ES), VIB-UGent Center for Inflammation Research (BE), Olivia Newton-John Cancer Wellness & Research Centre (AU), Institut de Biologia Molecular de Barcelona (ES), Toronto Metropolitan University (CA)
Openalex Percentile: Top 54%
Phagocytosis and Immune Regulation
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