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Updated: Jul 22, 2025

Quantification of Efferocytosis by Single-cell Fluorescence Microscopy
Published on: August 18, 2018
Apoptotic exosome-like vesicles transfer specific and functional mRNAs to endothelial cells by
Alexandre Brodeur1,2,3, Francis Migneault1,2, Maude Lanoie1,2,3
1Centre de Recherche, Centre Hospitalier de l'Université de Montréal (CRCHUM) and Université de Montréal, Montréal, QC, Canada.
Abstract:
Apoptosis of endothelial cells prompts the release of apoptotic exosome-like vesicles (ApoExos), subtype extracellular vesicles secreted by apoptotic cells after caspase-3 activation. ApoExos are different from both apoptotic bodies and classical exosomes in their protein and nucleic acid contents and functions. In contrast to classical apoptotic bodies, ApoExos induce immunogenic responses that can be maladaptive when not tightly regulated. In the present study, we elucidated the mechanisms by which ApoExos are internalized by endothelial cells, which leads to shared specific and functional mRNAs of importance to endothelial function. Using flow cytometry and confocal microscopy, we revealed that ApoExos were actively internalized by endothelial cells. SiRNA-induced inhibition of classical endocytosis pathways with pharmacological inhibitors showed that ApoExos were internalized via phosphatidylserine-dependent macropinocytosis independently of classical endocytosis pathways. An electron microscopy analysis revealed that ApoExos increased the macropinocytosis rate in endothelial cells, setting in motion a positive feedback loop that increased the amount of internalized ApoExos. Deep sequencing of total RNA revealed that ApoExos possessed a unique protein-coding RNA profile, with PCSK5 being the most abundant mRNA. Internalization of ApoExos by cells led to the transfer of this RNA content from the ApoExos to cells. Specifically, PCSK5 mRNA was transferred to cells that had taken up ApoExos, and these cells subsequently expressed PCSK5. Collectively, our findings suggest that macropinocytosis is an effective entry pathway for the delivery of RNAs carried by ApoExos and that these RNAs are functionally expressed by the endothelial cells that internalize them. As ApoExos express a specific mRNA signature, these results suggest new avenues to understand how ApoExos produced at sites of vascular injury impact vascular function.
Insights
Apoptotic exosome-like vesicles (ApoExos) are actively internalized by endothelial cells via macropinocytosis, delivering functional mRNA and impacting vascular function.
Area of Science:
- Cell Biology
- Extracellular Vesicles
- Molecular Biology
Background:
- Apoptosis of endothelial cells releases apoptotic exosome-like vesicles (ApoExos).
- ApoExos differ from apoptotic bodies and exosomes in content and function.
- ApoExos can induce immunogenic responses.
Purpose of the Study:
- To elucidate the internalization mechanisms of ApoExos by endothelial cells.
- To determine the functional consequences of ApoExos internalization.
- To investigate the RNA transfer and expression from ApoExos to endothelial cells.
Main Methods:
- Flow cytometry and confocal microscopy to assess ApoExos uptake.
- siRNA inhibition and pharmacological agents to study endocytosis pathways.
- Electron microscopy to analyze macropinocytosis rates.
- Deep sequencing of total RNA to profile ApoExos mRNA content.
Main Results:
- ApoExos are actively internalized by endothelial cells via phosphatidylserine-dependent macropinocytosis.
- ApoExos increase the macropinocytosis rate in endothelial cells, creating a positive feedback loop.
- ApoExos contain unique mRNA profiles, with PCSK5 being the most abundant.
- Internalized ApoExos transfer functional PCSK5 mRNA to endothelial cells, leading to PCSK5 expression.
Conclusions:
- Macropinocytosis is a key pathway for ApoExos internalization and RNA delivery to endothelial cells.
- Delivered ApoExos RNAs are functionally expressed by recipient endothelial cells.
- ApoExos' specific mRNA signature offers insights into their role in vascular injury and function.
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