Essential role of phosphatidylserine externalization in apoptosing cell phagocytosis by macrophages
Abstract
In many apoptotic cells, phosphatidylserine (PS), that is normally restricted to the inner membrane layer, is externalized and subsequently recognized by phagocytes. However, it has been unclear whether PS externalization is sufficient for phagocytosis induction. In a cultured cell line undergoing Fas-mediated apoptosis, PS externalization preceded other apoptotic events. When transbilayer movement of membrane phospholipids was analyzed, a decrease of the uptake of PS and phosphatidylethanolamine and an increase of phosphatidylcholine incorporation were observed upon apoptosis induction. Apoptotic cultured cells were phagocytosed by macrophages in a manner dependent on externalized PS before plasma membrane permeability increased. Moreover, a N-ethylmaleimide treatment caused PS externalization independent of apoptosis, and such cells underwent PS-mediated phagocytosis. These results suggested that PS is externalized as a result of membrane phospholipid redistribution and externalized PS by itself induces apoptosing cell phagocytosis.
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Phosphatidylserine and phosphatidylethanolamine are known to play important roles in macrophage mobility, phagocytosis, and apoptosis.
“these lipid subspecies are known to play important roles in Mθ mobility, phagocytosis, and apoptosis (Greenberg et al., 2006; Marino and Kroemer, 2013; Shiratsuchi et al., 1998).”
From Genetic dissection of the impact of miR-33a and miR-33b during the progression of atherosclerosis (2017) · cites this paper as Shiratsuchi et al., 1998
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Genetic dissection of the impact of miR-33a and miR-33b during the progression of atherosclerosis
Price, N. L., Rotllan, N., Canfrán-Duque, A., Zhang, X., Pati, P., Arias, N., Moen, J., Mayr, M., Ford, D. A., Baldán, Á., et al. (2017) · Cell reports · doi:10.1016/j.celrep.2017.10.023 · Cited by 129 · see citing works
Shiratsuchi, A., Watanabe, I., Takeuchi, O., Akira, S., & Nakanishi, Y. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.4.2039 · Cited by 112 · see citing works
Self-citation
- Authors
- Shiratsuchi, A., Osada, S., Kanazawa, S., & Nakanishi, Y.
- Affiliations
- Kanazawa University (JP)
- Kaken Pharmaceutical (Japan) (JP)
- Corresponding author
- Nakanishi, Yoshinobu
- Venue
- Biochemical and Biophysical Research Communications
- Publisher
- Elsevier BV
- Published
- 1998-05
- Volume
- 246
- Issue
- 2
- Pages
- 549-555
- ISSN
- 0006-291X (ISSN-L)
- OpenAlex
- W2083725875
- Cited by
- 86
- References
- 0
- Citations by year
- 2026: 3 · 2024: 5 · 2023: 2 · 2022: 1 · 2021: 3 · 2019: 2 · 2018: 4 · 2017: 6 · 2016: 4 · 2015: 2 · 2013: 2
- FWCI
- 2.03
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biochemical and Biophysical Research Communications (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Japan Science Society
- 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 › Lipid Membrane Structure and Behavior
- Keywords
- phosphatidylserine exposure, phagocytosis of apoptotic cells, macrophages, Fas-mediated apoptosis, plasma membrane permeability, N-ethylmaleimide, phosphatidylethanolamine, phosphatidylcholine
- MeSH terms
- Animals, Cell Line, Cell Membrane Permeability, Ethylmaleimide, Female, HeLa Cells, Humans, Membrane Lipids, Phagocytosis, Phosphatidylserines, Transfection, Apoptosis, Macrophages, Peritoneal, fas Receptor, Mice, In Vitro Techniques
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