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Coronin involved in phagocytosis: Dynamics of particle-induced relocalization visualized by a green fluorescent protein tag
Open accessAbstract
Coronin is a protein involved in cell locomotion and cytokinesis of Dictyostelium discoideum. Here we show that coronin is strongly enriched in phagocytic cups formed in response to particle attachment. A fusion of coronin with green fluorescent protein (GFP) accumulates in the cups within less than 1 min upon attachment of a particle and is gradually released from the phagosome within 1 min after engulfment is completed. Phagocytic cup formation competes with leading edge formation and can be interrupted at any stage. When the cup regresses, coronin dissociates from the site of accumulation. TRITC-labeled yeast cells have been used to assay phagocytosis quantitatively in wild-type and coronin-null cells. In the mutant, the rate of uptake is reduced to about one third, which shows that coronin contributes to the efficiency of phagocytosis to about the same extent as it improves the speed of cell locomotion.
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“Molecular mechanisms of phagocytosis are conserved throughout evolution.”
From Genome-wide transcriptional changes induced by phagocytosis or growth on bacteria in Dictyostelium (2008) · cites this paper as [4]
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“On the other hand, despite many actin-binding proteins and myosin I isoforms are transiently recruited to phagosomes, only a handful of them have been shown by gene knock-out experiments to affect phagocytosis, possibly due to redundancy of the system [4,9,57-59].”
From Genome-wide transcriptional changes induced by phagocytosis or growth on bacteria in Dictyostelium (2008) · cites this paper as [4]
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A Dictyostelium Mutant with Reduced Lysozyme Levels Compensates by Increased Phagocytic Activity
Müller, I., Šubert, N., Otto, H., Herbst, R., Rühling, H., Maniak, M., & Leippe, M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m411445200 · Cited by 35
Self-citationPhagosomal Proteins of Dictyostelium discoideum
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Severe developmental defects in Dictyostelium null mutants for actin-binding proteins
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Fluorescent Reporters and Methods to Analyze Fluorescent Signals
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Metadata
- Authors
- Maniak, M., Rauchenberger, R., Albrecht, R., Murphy, J., & Gerisch, G.
- Affiliations
- Max Planck Institute of Biochemistry (DE)
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1995-12
- Volume
- 83
- Issue
- 6
- Pages
- 915-924
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W1989760629
- Cited by
- 354
- References
- 43
- Citations by year
- 2026: 4 · 2025: 2 · 2024: 3 · 2023: 1 · 2022: 2 · 2021: 8 · 2020: 4 · 2019: 5 · 2018: 3 · 2017: 5 · 2016: 5 · 2015: 4 · 2014: 11 · 2013: 8 · 2012: 8
- FWCI
- 5.02
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Slime Mold and Myxomycetes Research
- Keywords
- coronin, phagocytosis, phagocytic cup, phagosome, Dictyostelium discoideum, GFP fusion protein, cell locomotion
- MeSH terms
- Actinin, Actins, Animals, Carrier Proteins, Cell Membrane, Cytochalasins, Cytoplasm, Dictyostelium, Fungal Proteins, Indicators and Reagents, Luminescent Proteins, Microfilament Proteins, Phagocytosis, Phagosomes, Saccharomyces cerevisiae, Protozoan Proteins, Green Fluorescent Proteins
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