Annexin I Is an Endogenous Ligand that Mediates Apoptotic Cell Engulfment
Open accessAbstract
Engulfment of apoptotic cells requires presentation of new cell surface ligands by the dying cells. Using a differential proteomics technology, we identify that annexin I is a caspase-dependent engulfment ligand; it is recruited from the cytosol and exported to the outer plasma membrane leaflet, colocalizes with phosphatidylserine, and is required for efficient clearance of apoptotic cells. Furthermore, phosphatidylserine receptor (PSR) clustering around apoptotic cells indicates a requirement for annexin I. In the nematode Caenorhabditis elegans, downregulation of the annexin homolog prevents efficient engulfment of pharyngeal cell corpses. These results provide novel mechanistic insights into how apoptotic cells are removed and may explain a pathogenic mechanism of chronic inflammatory diseases where annexin I autoantibodies have been described.
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Evidence supports roles for Annexin I and Gas-6 in recognizing phosphatidylserine on dying cells.
“Evidence also supports roles for Annexin I 122 and Gas-6 123 in recognizing PS on dying cells.”
From Immunogenic and tolerogenic cell death (2009) · cites this paper as [123]
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References 53 · Cited by 434
- Authors
- Arur, S., Uche, U. E., Rezaul, K., Fong, M., Scranton, V., Cowan, A. E., Mohler, W., & Han, D. K.
- Affiliations
- University of Connecticut (US)
- Corresponding author
- Han, David K.
- Venue
- Developmental Cell
- Publisher
- Elsevier BV
- Published
- 2003-04
- Volume
- 4
- Issue
- 4
- Pages
- 587-598
- ISSN
- 1534-5807 (ISSN-L)
- OpenAlex
- W2032946509
- Cited by
- 434
- References
- 53
- Citations by year
- 2026: 3 · 2025: 18 · 2024: 9 · 2023: 11 · 2022: 11 · 2021: 15 · 2020: 12 · 2019: 17 · 2018: 20 · 2017: 19 · 2016: 27 · 2015: 17 · 2014: 19 · 2013: 22 · 2012: 17
- FWCI
- 9.98
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 3760 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Developmental Cell (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (PO1 HL70694, RO1 HL 67569, RR13186)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › S100 Proteins and Annexins
- Keywords
- annexin A1, apoptotic cell engulfment, phosphatidylserine, phosphatidylserine receptor, efferocytosis, Caenorhabditis elegans, chronic inflammatory diseases
- MeSH terms
- Animals, Cell Membrane, Eukaryotic Cells, Humans, Ligands, Membrane Proteins, Peptide Fragments, Phagocytosis, Receptors, Cell Surface, Signal Transduction, Down-Regulation, Helminth Proteins, Up-Regulation, Caenorhabditis elegans, Apoptosis, Annexins, Annexin A1, Jurkat Cells, Calcium Signaling, Caspases, Protein Transport, Cell Membrane Structures, Caenorhabditis elegans Proteins, Jumonji Domain-Containing Histone Demethylases
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