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Shape-Shifted Red Blood Cells: A Novel Red Blood Cell Stage?

Primitive nucleated erythroid cells in the bloodstream have long been suggested to be more similar to nucleated red cells of fish, amphibians, and birds than the red cells of fetal and adult mammals. Rainbow trout Ficoll-purified red blood cells (RBCs) cultured in vitro undergo morphological changes...

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Autores principales: Chico, Verónica, Puente-Marin, Sara, Nombela, Iván, Ciordia, Sergio, Mena, María Carmen, Carracedo, Begoña, Villena, Alberto, Mercado, Luis, Coll, Julio, Ortega-Villaizan, María del Mar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946108/
https://www.ncbi.nlm.nih.gov/pubmed/29671811
http://dx.doi.org/10.3390/cells7040031
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author Chico, Verónica
Puente-Marin, Sara
Nombela, Iván
Ciordia, Sergio
Mena, María Carmen
Carracedo, Begoña
Villena, Alberto
Mercado, Luis
Coll, Julio
Ortega-Villaizan, María del Mar
author_facet Chico, Verónica
Puente-Marin, Sara
Nombela, Iván
Ciordia, Sergio
Mena, María Carmen
Carracedo, Begoña
Villena, Alberto
Mercado, Luis
Coll, Julio
Ortega-Villaizan, María del Mar
author_sort Chico, Verónica
collection PubMed
description Primitive nucleated erythroid cells in the bloodstream have long been suggested to be more similar to nucleated red cells of fish, amphibians, and birds than the red cells of fetal and adult mammals. Rainbow trout Ficoll-purified red blood cells (RBCs) cultured in vitro undergo morphological changes, especially when exposed to stress, and enter a new cell stage that we have coined shape-shifted RBCs (shRBCs). We have characterized these shRBCs using transmission electron microscopy (TEM) micrographs, Wright–Giemsa staining, cell marker immunostaining, and transcriptomic and proteomic evaluation. shRBCs showed reduced density of the cytoplasm, hemoglobin loss, decondensed chromatin in the nucleus, and striking expression of the B lymphocyte molecular marker IgM. In addition, shRBCs shared some features of mammalian primitive pyrenocytes (extruded nucleus surrounded by a thin rim of cytoplasm and phosphatidylserine (PS) exposure on cell surface). These shRBCs were transiently observed in heat-stressed rainbow trout bloodstream for three days. Functional network analysis of combined transcriptomic and proteomic studies resulted in the identification of proteins involved in pathways related to the regulation of cell morphogenesis involved in differentiation, cellular response to stress, and immune system process. In addition, shRBCs increased interleukin 8 (IL8), interleukin 1 β (IL1β), interferon ɣ (IFNɣ), and natural killer enhancing factor (NKEF) protein production in response to viral hemorrhagic septicemia virus (VHSV). In conclusion, shRBCs may represent a novel cell stage that participates in roles related to immune response mediation, homeostasis, and the differentiation and development of blood cells.
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spelling pubmed-59461082018-05-15 Shape-Shifted Red Blood Cells: A Novel Red Blood Cell Stage? Chico, Verónica Puente-Marin, Sara Nombela, Iván Ciordia, Sergio Mena, María Carmen Carracedo, Begoña Villena, Alberto Mercado, Luis Coll, Julio Ortega-Villaizan, María del Mar Cells Article Primitive nucleated erythroid cells in the bloodstream have long been suggested to be more similar to nucleated red cells of fish, amphibians, and birds than the red cells of fetal and adult mammals. Rainbow trout Ficoll-purified red blood cells (RBCs) cultured in vitro undergo morphological changes, especially when exposed to stress, and enter a new cell stage that we have coined shape-shifted RBCs (shRBCs). We have characterized these shRBCs using transmission electron microscopy (TEM) micrographs, Wright–Giemsa staining, cell marker immunostaining, and transcriptomic and proteomic evaluation. shRBCs showed reduced density of the cytoplasm, hemoglobin loss, decondensed chromatin in the nucleus, and striking expression of the B lymphocyte molecular marker IgM. In addition, shRBCs shared some features of mammalian primitive pyrenocytes (extruded nucleus surrounded by a thin rim of cytoplasm and phosphatidylserine (PS) exposure on cell surface). These shRBCs were transiently observed in heat-stressed rainbow trout bloodstream for three days. Functional network analysis of combined transcriptomic and proteomic studies resulted in the identification of proteins involved in pathways related to the regulation of cell morphogenesis involved in differentiation, cellular response to stress, and immune system process. In addition, shRBCs increased interleukin 8 (IL8), interleukin 1 β (IL1β), interferon ɣ (IFNɣ), and natural killer enhancing factor (NKEF) protein production in response to viral hemorrhagic septicemia virus (VHSV). In conclusion, shRBCs may represent a novel cell stage that participates in roles related to immune response mediation, homeostasis, and the differentiation and development of blood cells. MDPI 2018-04-19 /pmc/articles/PMC5946108/ /pubmed/29671811 http://dx.doi.org/10.3390/cells7040031 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chico, Verónica
Puente-Marin, Sara
Nombela, Iván
Ciordia, Sergio
Mena, María Carmen
Carracedo, Begoña
Villena, Alberto
Mercado, Luis
Coll, Julio
Ortega-Villaizan, María del Mar
Shape-Shifted Red Blood Cells: A Novel Red Blood Cell Stage?
title Shape-Shifted Red Blood Cells: A Novel Red Blood Cell Stage?
title_full Shape-Shifted Red Blood Cells: A Novel Red Blood Cell Stage?
title_fullStr Shape-Shifted Red Blood Cells: A Novel Red Blood Cell Stage?
title_full_unstemmed Shape-Shifted Red Blood Cells: A Novel Red Blood Cell Stage?
title_short Shape-Shifted Red Blood Cells: A Novel Red Blood Cell Stage?
title_sort shape-shifted red blood cells: a novel red blood cell stage?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946108/
https://www.ncbi.nlm.nih.gov/pubmed/29671811
http://dx.doi.org/10.3390/cells7040031
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