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Allorecognition Triggers Autophagy and Subsequent Necrosis in the Cnidarian Hydractinia symbiolongicarpus
Transitory fusion is an allorecognition phenotype displayed by the colonial hydroid Hydractinia symbiolongicarpus when interacting colonies share some, but not all, loci within the allorecognition gene complex (ARC). The phenotype is characterized by an initial fusion followed by subsequent cell dea...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493586/ https://www.ncbi.nlm.nih.gov/pubmed/23145018 http://dx.doi.org/10.1371/journal.pone.0048914 |
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author | Buss, Leo W. Anderson, Christopher Westerman, Erica Kritzberger, Chad Poudyal, Monita Moreno, Maria A. Lakkis, Fadi G. |
author_facet | Buss, Leo W. Anderson, Christopher Westerman, Erica Kritzberger, Chad Poudyal, Monita Moreno, Maria A. Lakkis, Fadi G. |
author_sort | Buss, Leo W. |
collection | PubMed |
description | Transitory fusion is an allorecognition phenotype displayed by the colonial hydroid Hydractinia symbiolongicarpus when interacting colonies share some, but not all, loci within the allorecognition gene complex (ARC). The phenotype is characterized by an initial fusion followed by subsequent cell death resulting in separation of the two incompatible colonies. We here characterize this cell death process using scanning electron microscopy (SEM), transmission electron microscopy (TEM), and continuous in vivo digital microscopy. These techniques reveal widespread autophagy and subsequent necrosis in both colony and grafted polyp assays. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assays and ultrastructural observations revealed no evidence of apoptosis. Pharmacological inhibition of autophagy using 3-methyladenine (3-MA) completely suppressed transitory fusion in vivo in colony assays. Rapamycin did not have a significant effect in the same assays. These results establish the hydroid allorecognition system as a novel model for the study of cell death. |
format | Online Article Text |
id | pubmed-3493586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34935862012-11-09 Allorecognition Triggers Autophagy and Subsequent Necrosis in the Cnidarian Hydractinia symbiolongicarpus Buss, Leo W. Anderson, Christopher Westerman, Erica Kritzberger, Chad Poudyal, Monita Moreno, Maria A. Lakkis, Fadi G. PLoS One Research Article Transitory fusion is an allorecognition phenotype displayed by the colonial hydroid Hydractinia symbiolongicarpus when interacting colonies share some, but not all, loci within the allorecognition gene complex (ARC). The phenotype is characterized by an initial fusion followed by subsequent cell death resulting in separation of the two incompatible colonies. We here characterize this cell death process using scanning electron microscopy (SEM), transmission electron microscopy (TEM), and continuous in vivo digital microscopy. These techniques reveal widespread autophagy and subsequent necrosis in both colony and grafted polyp assays. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assays and ultrastructural observations revealed no evidence of apoptosis. Pharmacological inhibition of autophagy using 3-methyladenine (3-MA) completely suppressed transitory fusion in vivo in colony assays. Rapamycin did not have a significant effect in the same assays. These results establish the hydroid allorecognition system as a novel model for the study of cell death. Public Library of Science 2012-11-08 /pmc/articles/PMC3493586/ /pubmed/23145018 http://dx.doi.org/10.1371/journal.pone.0048914 Text en © 2012 Buss et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Buss, Leo W. Anderson, Christopher Westerman, Erica Kritzberger, Chad Poudyal, Monita Moreno, Maria A. Lakkis, Fadi G. Allorecognition Triggers Autophagy and Subsequent Necrosis in the Cnidarian Hydractinia symbiolongicarpus |
title | Allorecognition Triggers Autophagy and Subsequent Necrosis in the Cnidarian Hydractinia symbiolongicarpus
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title_full | Allorecognition Triggers Autophagy and Subsequent Necrosis in the Cnidarian Hydractinia symbiolongicarpus
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title_fullStr | Allorecognition Triggers Autophagy and Subsequent Necrosis in the Cnidarian Hydractinia symbiolongicarpus
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title_full_unstemmed | Allorecognition Triggers Autophagy and Subsequent Necrosis in the Cnidarian Hydractinia symbiolongicarpus
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title_short | Allorecognition Triggers Autophagy and Subsequent Necrosis in the Cnidarian Hydractinia symbiolongicarpus
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title_sort | allorecognition triggers autophagy and subsequent necrosis in the cnidarian hydractinia symbiolongicarpus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493586/ https://www.ncbi.nlm.nih.gov/pubmed/23145018 http://dx.doi.org/10.1371/journal.pone.0048914 |
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