Cargando…
Fish and Mammalian Phagocytes Differentially Regulate Pro-Inflammatory and Homeostatic Responses In Vivo
Phagocytosis is a cellular mechanism that is important to the early induction of antimicrobial responses and the regulation of adaptive immunity. At an inflammatory site, phagocytes serve as central regulators for both pro-inflammatory and homeostatic anti-inflammatory processes. However, it remains...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3479104/ https://www.ncbi.nlm.nih.gov/pubmed/23110059 http://dx.doi.org/10.1371/journal.pone.0047070 |
_version_ | 1782247404231196672 |
---|---|
author | Rieger, Aja M. Konowalchuk, Jeffrey D. Grayfer, Leon Katzenback, Barbara A. Havixbeck, Jeffrey J. Kiemele, Moira D. Belosevic, Miodrag Barreda, Daniel R. |
author_facet | Rieger, Aja M. Konowalchuk, Jeffrey D. Grayfer, Leon Katzenback, Barbara A. Havixbeck, Jeffrey J. Kiemele, Moira D. Belosevic, Miodrag Barreda, Daniel R. |
author_sort | Rieger, Aja M. |
collection | PubMed |
description | Phagocytosis is a cellular mechanism that is important to the early induction of antimicrobial responses and the regulation of adaptive immunity. At an inflammatory site, phagocytes serve as central regulators for both pro-inflammatory and homeostatic anti-inflammatory processes. However, it remains unclear if this is a recent evolutionary development or whether the capacity to balance between these two seemingly contradictory processes is a feature already displayed in lower vertebrates. In this study, we used murine (C57BL/6) and teleost fish (C. auratus) in vitro and in vivo models to assess the evolutionary conservation of this dichotomy at a site of inflammation. At the level of the macrophage, we found that teleost fish already displayed divergent pro-inflammatory and homeostatic responses following internalization of zymosan or apoptotic bodies, respectively, and that these were consistent with those of mice. However, fish and mice displayed significant differences in vivo with regards to the level of responsiveness to zymosan and apoptotic bodies, the identity of infiltrating leukocytes, their rate of infiltration, and the kinetics and strength of resulting antimicrobial responses. Unlike macrophages, significant differences were identified between teleost and murine neutrophilic responses. We report for the first time that activated murine, but not teleost neutrophils, possess the capacity to internalize apoptotic bodies. This internalization translates into reduction of neutrophil ROS production. This may play an important part in the recently identified anti-inflammatory activity that mammalian neutrophils display during the resolution phase of inflammation. Our observations are consistent with continued honing of inflammatory control mechanisms from fish to mammals, and provide added insights into the evolutionary path that has resulted in the integrated, multilayered responses that are characteristic of higher vertebrates. |
format | Online Article Text |
id | pubmed-3479104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34791042012-10-29 Fish and Mammalian Phagocytes Differentially Regulate Pro-Inflammatory and Homeostatic Responses In Vivo Rieger, Aja M. Konowalchuk, Jeffrey D. Grayfer, Leon Katzenback, Barbara A. Havixbeck, Jeffrey J. Kiemele, Moira D. Belosevic, Miodrag Barreda, Daniel R. PLoS One Research Article Phagocytosis is a cellular mechanism that is important to the early induction of antimicrobial responses and the regulation of adaptive immunity. At an inflammatory site, phagocytes serve as central regulators for both pro-inflammatory and homeostatic anti-inflammatory processes. However, it remains unclear if this is a recent evolutionary development or whether the capacity to balance between these two seemingly contradictory processes is a feature already displayed in lower vertebrates. In this study, we used murine (C57BL/6) and teleost fish (C. auratus) in vitro and in vivo models to assess the evolutionary conservation of this dichotomy at a site of inflammation. At the level of the macrophage, we found that teleost fish already displayed divergent pro-inflammatory and homeostatic responses following internalization of zymosan or apoptotic bodies, respectively, and that these were consistent with those of mice. However, fish and mice displayed significant differences in vivo with regards to the level of responsiveness to zymosan and apoptotic bodies, the identity of infiltrating leukocytes, their rate of infiltration, and the kinetics and strength of resulting antimicrobial responses. Unlike macrophages, significant differences were identified between teleost and murine neutrophilic responses. We report for the first time that activated murine, but not teleost neutrophils, possess the capacity to internalize apoptotic bodies. This internalization translates into reduction of neutrophil ROS production. This may play an important part in the recently identified anti-inflammatory activity that mammalian neutrophils display during the resolution phase of inflammation. Our observations are consistent with continued honing of inflammatory control mechanisms from fish to mammals, and provide added insights into the evolutionary path that has resulted in the integrated, multilayered responses that are characteristic of higher vertebrates. Public Library of Science 2012-10-23 /pmc/articles/PMC3479104/ /pubmed/23110059 http://dx.doi.org/10.1371/journal.pone.0047070 Text en © 2012 Rieger 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 Rieger, Aja M. Konowalchuk, Jeffrey D. Grayfer, Leon Katzenback, Barbara A. Havixbeck, Jeffrey J. Kiemele, Moira D. Belosevic, Miodrag Barreda, Daniel R. Fish and Mammalian Phagocytes Differentially Regulate Pro-Inflammatory and Homeostatic Responses In Vivo |
title | Fish and Mammalian Phagocytes Differentially Regulate Pro-Inflammatory and Homeostatic Responses In Vivo
|
title_full | Fish and Mammalian Phagocytes Differentially Regulate Pro-Inflammatory and Homeostatic Responses In Vivo
|
title_fullStr | Fish and Mammalian Phagocytes Differentially Regulate Pro-Inflammatory and Homeostatic Responses In Vivo
|
title_full_unstemmed | Fish and Mammalian Phagocytes Differentially Regulate Pro-Inflammatory and Homeostatic Responses In Vivo
|
title_short | Fish and Mammalian Phagocytes Differentially Regulate Pro-Inflammatory and Homeostatic Responses In Vivo
|
title_sort | fish and mammalian phagocytes differentially regulate pro-inflammatory and homeostatic responses in vivo |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3479104/ https://www.ncbi.nlm.nih.gov/pubmed/23110059 http://dx.doi.org/10.1371/journal.pone.0047070 |
work_keys_str_mv | AT riegerajam fishandmammalianphagocytesdifferentiallyregulateproinflammatoryandhomeostaticresponsesinvivo AT konowalchukjeffreyd fishandmammalianphagocytesdifferentiallyregulateproinflammatoryandhomeostaticresponsesinvivo AT grayferleon fishandmammalianphagocytesdifferentiallyregulateproinflammatoryandhomeostaticresponsesinvivo AT katzenbackbarbaraa fishandmammalianphagocytesdifferentiallyregulateproinflammatoryandhomeostaticresponsesinvivo AT havixbeckjeffreyj fishandmammalianphagocytesdifferentiallyregulateproinflammatoryandhomeostaticresponsesinvivo AT kiemelemoirad fishandmammalianphagocytesdifferentiallyregulateproinflammatoryandhomeostaticresponsesinvivo AT belosevicmiodrag fishandmammalianphagocytesdifferentiallyregulateproinflammatoryandhomeostaticresponsesinvivo AT barredadanielr fishandmammalianphagocytesdifferentiallyregulateproinflammatoryandhomeostaticresponsesinvivo |