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Updated: Jun 13, 2026

Quantification of Efferocytosis by Single-cell Fluorescence Microscopy
Published on: August 18, 2018
Measuring efferocytosis by intraperitoneal clearance assay
Caitlin L Vella1, Dilara C Ozkocak2, Amy A Baxter1
1La Trobe Institute for Molecular Science, Department of Biochemistry & Chemistry, School of Agriculture, Biomedicine and Environment, La Trobe University, Bundoora, VIC, Australia; School of Agriculture, Biomedicine and Environment, Centre for Cardiovascular Biology and Disease Research, La Trobe University, Bundoora, VIC, Australia.
Abstract:
Efferocytosis is a critical process by which phagocytes identify, engulf and clear apoptotic cells, thereby preserving immune tolerance and tissue homeostasis. While in vitro assays have advanced our understanding of the molecular mechanisms underlying apoptotic cell clearance, they lack the complexity of the physiological environment. This chapter presents a detailed in vivo approach for assessing efferocytosis by mouse peritoneal macrophages using the intraperitoneal (IP) clearance assay. By administering fluorescently labelled apoptotic Jurkat T cells into the peritoneal cavity, this method enables the quantification of apoptotic cell uptake in a native tissue context, capturing the influence of local immune signals, stromal interactions and systemic factors. This protocol is compatible with genetic and pharmacological manipulations, allowing researchers to investigate how various interventions affect efferocytic capacity. Overall, this approach provides a robust and physiologically relevant framework for studying efferocytosis and its implications in both homeostatic and pathological settings.

