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Functional Characterization of Hexacorallia Phagocytic Cells

Phagocytosis is the cellular defense mechanism used to eliminate antigens derived from dysregulated or damaged cells, and microbial pathogens. Phagocytosis is therefore a pillar of innate immunity, whereby foreign particles are engulfed and degraded in lysolitic vesicles. In hexacorallians, phagocyt...

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Autores principales: Snyder, Grace A., Eliachar, Shir, Connelly, Michael T., Talice, Shani, Hadad, Uzi, Gershoni-Yahalom, Orly, Browne, William E., Palmer, Caroline V., Rosental, Benyamin, Traylor-Knowles, Nikki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350327/
https://www.ncbi.nlm.nih.gov/pubmed/34381444
http://dx.doi.org/10.3389/fimmu.2021.662803
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author Snyder, Grace A.
Eliachar, Shir
Connelly, Michael T.
Talice, Shani
Hadad, Uzi
Gershoni-Yahalom, Orly
Browne, William E.
Palmer, Caroline V.
Rosental, Benyamin
Traylor-Knowles, Nikki
author_facet Snyder, Grace A.
Eliachar, Shir
Connelly, Michael T.
Talice, Shani
Hadad, Uzi
Gershoni-Yahalom, Orly
Browne, William E.
Palmer, Caroline V.
Rosental, Benyamin
Traylor-Knowles, Nikki
author_sort Snyder, Grace A.
collection PubMed
description Phagocytosis is the cellular defense mechanism used to eliminate antigens derived from dysregulated or damaged cells, and microbial pathogens. Phagocytosis is therefore a pillar of innate immunity, whereby foreign particles are engulfed and degraded in lysolitic vesicles. In hexacorallians, phagocytic mechanisms are poorly understood, though putative anthozoan phagocytic cells (amoebocytes) have been identified histologically. We identify and characterize phagocytes from the coral Pocillopora damicornis and the sea anemone Nematostella vectensis. Using fluorescence-activated cell sorting and microscopy, we show that distinct populations of phagocytic cells engulf bacteria, fungal antigens, and beads. In addition to pathogenic antigens, we show that phagocytic cells engulf self, damaged cells. We show that target antigens localize to low pH phagolysosomes, and that degradation is occurring within them. Inhibiting actin filament rearrangement interferes with efficient particle phagocytosis but does not affect small molecule pinocytosis. We also demonstrate that cellular markers for lysolitic vesicles and reactive oxygen species (ROS) correlate with hexacorallian phagocytes. These results establish a foundation for improving our understanding of hexacorallian immune cell biology.
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spelling pubmed-83503272021-08-10 Functional Characterization of Hexacorallia Phagocytic Cells Snyder, Grace A. Eliachar, Shir Connelly, Michael T. Talice, Shani Hadad, Uzi Gershoni-Yahalom, Orly Browne, William E. Palmer, Caroline V. Rosental, Benyamin Traylor-Knowles, Nikki Front Immunol Immunology Phagocytosis is the cellular defense mechanism used to eliminate antigens derived from dysregulated or damaged cells, and microbial pathogens. Phagocytosis is therefore a pillar of innate immunity, whereby foreign particles are engulfed and degraded in lysolitic vesicles. In hexacorallians, phagocytic mechanisms are poorly understood, though putative anthozoan phagocytic cells (amoebocytes) have been identified histologically. We identify and characterize phagocytes from the coral Pocillopora damicornis and the sea anemone Nematostella vectensis. Using fluorescence-activated cell sorting and microscopy, we show that distinct populations of phagocytic cells engulf bacteria, fungal antigens, and beads. In addition to pathogenic antigens, we show that phagocytic cells engulf self, damaged cells. We show that target antigens localize to low pH phagolysosomes, and that degradation is occurring within them. Inhibiting actin filament rearrangement interferes with efficient particle phagocytosis but does not affect small molecule pinocytosis. We also demonstrate that cellular markers for lysolitic vesicles and reactive oxygen species (ROS) correlate with hexacorallian phagocytes. These results establish a foundation for improving our understanding of hexacorallian immune cell biology. Frontiers Media S.A. 2021-07-26 /pmc/articles/PMC8350327/ /pubmed/34381444 http://dx.doi.org/10.3389/fimmu.2021.662803 Text en Copyright © 2021 Snyder, Eliachar, Connelly, Talice, Hadad, Gershoni-Yahalom, Browne, Palmer, Rosental and Traylor-Knowles https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Snyder, Grace A.
Eliachar, Shir
Connelly, Michael T.
Talice, Shani
Hadad, Uzi
Gershoni-Yahalom, Orly
Browne, William E.
Palmer, Caroline V.
Rosental, Benyamin
Traylor-Knowles, Nikki
Functional Characterization of Hexacorallia Phagocytic Cells
title Functional Characterization of Hexacorallia Phagocytic Cells
title_full Functional Characterization of Hexacorallia Phagocytic Cells
title_fullStr Functional Characterization of Hexacorallia Phagocytic Cells
title_full_unstemmed Functional Characterization of Hexacorallia Phagocytic Cells
title_short Functional Characterization of Hexacorallia Phagocytic Cells
title_sort functional characterization of hexacorallia phagocytic cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350327/
https://www.ncbi.nlm.nih.gov/pubmed/34381444
http://dx.doi.org/10.3389/fimmu.2021.662803
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