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Identification of Bipotential Blood Cell/Nephrocyte Progenitors in Drosophila: Another Route for Generating Blood Progenitors
The Drosophila lymph gland is the larval hematopoietic organ and is aligned along the anterior part of the cardiovascular system, composed of cardiac cells, that form the cardiac tube and its associated pericardial cells or nephrocytes. By the end of embryogenesis the lymph gland is composed of a si...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8883574/ https://www.ncbi.nlm.nih.gov/pubmed/35237606 http://dx.doi.org/10.3389/fcell.2022.834720 |
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author | Morin-Poulard, Ismaël Destalminil-Letourneau, Manon Bataillé, Laetitia Frendo, Jean-Louis Lebreton, Gaëlle Vanzo, Nathalie Crozatier, Michèle |
author_facet | Morin-Poulard, Ismaël Destalminil-Letourneau, Manon Bataillé, Laetitia Frendo, Jean-Louis Lebreton, Gaëlle Vanzo, Nathalie Crozatier, Michèle |
author_sort | Morin-Poulard, Ismaël |
collection | PubMed |
description | The Drosophila lymph gland is the larval hematopoietic organ and is aligned along the anterior part of the cardiovascular system, composed of cardiac cells, that form the cardiac tube and its associated pericardial cells or nephrocytes. By the end of embryogenesis the lymph gland is composed of a single pair of lobes. Two additional pairs of posterior lobes develop during larval development to contribute to the mature lymph gland. In this study we describe the ontogeny of lymph gland posterior lobes during larval development and identify the genetic basis of the process. By lineage tracing we show here that each posterior lobe originates from three embryonic pericardial cells, thus establishing a bivalent blood cell/nephrocyte potential for a subset of embryonic pericardial cells. The posterior lobes of L3 larvae posterior lobes are composed of heterogeneous blood progenitors and their diversity is progressively built during larval development. We further establish that in larvae, homeotic genes and the transcription factor Klf15 regulate the choice between blood cell and nephrocyte fates. Our data underline the sequential production of blood cell progenitors during larval development. |
format | Online Article Text |
id | pubmed-8883574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88835742022-03-01 Identification of Bipotential Blood Cell/Nephrocyte Progenitors in Drosophila: Another Route for Generating Blood Progenitors Morin-Poulard, Ismaël Destalminil-Letourneau, Manon Bataillé, Laetitia Frendo, Jean-Louis Lebreton, Gaëlle Vanzo, Nathalie Crozatier, Michèle Front Cell Dev Biol Cell and Developmental Biology The Drosophila lymph gland is the larval hematopoietic organ and is aligned along the anterior part of the cardiovascular system, composed of cardiac cells, that form the cardiac tube and its associated pericardial cells or nephrocytes. By the end of embryogenesis the lymph gland is composed of a single pair of lobes. Two additional pairs of posterior lobes develop during larval development to contribute to the mature lymph gland. In this study we describe the ontogeny of lymph gland posterior lobes during larval development and identify the genetic basis of the process. By lineage tracing we show here that each posterior lobe originates from three embryonic pericardial cells, thus establishing a bivalent blood cell/nephrocyte potential for a subset of embryonic pericardial cells. The posterior lobes of L3 larvae posterior lobes are composed of heterogeneous blood progenitors and their diversity is progressively built during larval development. We further establish that in larvae, homeotic genes and the transcription factor Klf15 regulate the choice between blood cell and nephrocyte fates. Our data underline the sequential production of blood cell progenitors during larval development. Frontiers Media S.A. 2022-02-14 /pmc/articles/PMC8883574/ /pubmed/35237606 http://dx.doi.org/10.3389/fcell.2022.834720 Text en Copyright © 2022 Morin-Poulard, Destalminil-Letourneau, Bataillé, Frendo, Lebreton, Vanzo and Crozatier. 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 | Cell and Developmental Biology Morin-Poulard, Ismaël Destalminil-Letourneau, Manon Bataillé, Laetitia Frendo, Jean-Louis Lebreton, Gaëlle Vanzo, Nathalie Crozatier, Michèle Identification of Bipotential Blood Cell/Nephrocyte Progenitors in Drosophila: Another Route for Generating Blood Progenitors |
title | Identification of Bipotential Blood Cell/Nephrocyte Progenitors in Drosophila: Another Route for Generating Blood Progenitors |
title_full | Identification of Bipotential Blood Cell/Nephrocyte Progenitors in Drosophila: Another Route for Generating Blood Progenitors |
title_fullStr | Identification of Bipotential Blood Cell/Nephrocyte Progenitors in Drosophila: Another Route for Generating Blood Progenitors |
title_full_unstemmed | Identification of Bipotential Blood Cell/Nephrocyte Progenitors in Drosophila: Another Route for Generating Blood Progenitors |
title_short | Identification of Bipotential Blood Cell/Nephrocyte Progenitors in Drosophila: Another Route for Generating Blood Progenitors |
title_sort | identification of bipotential blood cell/nephrocyte progenitors in drosophila: another route for generating blood progenitors |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8883574/ https://www.ncbi.nlm.nih.gov/pubmed/35237606 http://dx.doi.org/10.3389/fcell.2022.834720 |
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