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Hemocytes and fat body cells, the only professional immune cell types in Drosophila, show strikingly different responses to systemic infections
The fruit fly Drosophila is an excellent model to study the response of different immunocompetent organs during systemic infection. In the present study, we intended to test the hypothesis that the only professional immune organs of the fly, the fat body and hemocytes, show substantial similarities...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9726733/ https://www.ncbi.nlm.nih.gov/pubmed/36505446 http://dx.doi.org/10.3389/fimmu.2022.1040510 |
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author | Vaibhvi, Vaibhvi Künzel, Sven Roeder, Thomas |
author_facet | Vaibhvi, Vaibhvi Künzel, Sven Roeder, Thomas |
author_sort | Vaibhvi, Vaibhvi |
collection | PubMed |
description | The fruit fly Drosophila is an excellent model to study the response of different immunocompetent organs during systemic infection. In the present study, we intended to test the hypothesis that the only professional immune organs of the fly, the fat body and hemocytes, show substantial similarities in their responses to systemic infection. However, comprehensive transcriptome analysis of isolated organs revealed highly divergent transcript signatures, with the few commonly regulated genes encoding mainly classical immune effectors from the antimicrobial peptide family. The fat body and the hemocytes each have specific reactions that are not present in the other organ. Fat body-specific responses comprised those enabling an improved peptide synthesis and export. This reaction is accompanied by transcriptomic shifts enabling the use of the energy resources of the fat body more efficiently. Hemocytes, on the other hand, showed enhanced signatures related to phagocytosis. Comparing immune-induced signatures of both cell types with those of whole-body responses showed only a minimal correspondence, mostly restricted again to antimicrobial peptide genes. In summary, the two major immunocompetent cell types of Drosophila show highly specific responses to infection, which are closely linked to the primary function of the respective organ in the landscape of the systemic immune response. |
format | Online Article Text |
id | pubmed-9726733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97267332022-12-08 Hemocytes and fat body cells, the only professional immune cell types in Drosophila, show strikingly different responses to systemic infections Vaibhvi, Vaibhvi Künzel, Sven Roeder, Thomas Front Immunol Immunology The fruit fly Drosophila is an excellent model to study the response of different immunocompetent organs during systemic infection. In the present study, we intended to test the hypothesis that the only professional immune organs of the fly, the fat body and hemocytes, show substantial similarities in their responses to systemic infection. However, comprehensive transcriptome analysis of isolated organs revealed highly divergent transcript signatures, with the few commonly regulated genes encoding mainly classical immune effectors from the antimicrobial peptide family. The fat body and the hemocytes each have specific reactions that are not present in the other organ. Fat body-specific responses comprised those enabling an improved peptide synthesis and export. This reaction is accompanied by transcriptomic shifts enabling the use of the energy resources of the fat body more efficiently. Hemocytes, on the other hand, showed enhanced signatures related to phagocytosis. Comparing immune-induced signatures of both cell types with those of whole-body responses showed only a minimal correspondence, mostly restricted again to antimicrobial peptide genes. In summary, the two major immunocompetent cell types of Drosophila show highly specific responses to infection, which are closely linked to the primary function of the respective organ in the landscape of the systemic immune response. Frontiers Media S.A. 2022-11-23 /pmc/articles/PMC9726733/ /pubmed/36505446 http://dx.doi.org/10.3389/fimmu.2022.1040510 Text en Copyright © 2022 Vaibhvi, Künzel and Roeder 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 Vaibhvi, Vaibhvi Künzel, Sven Roeder, Thomas Hemocytes and fat body cells, the only professional immune cell types in Drosophila, show strikingly different responses to systemic infections |
title | Hemocytes and fat body cells, the only professional immune cell types in Drosophila, show strikingly different responses to systemic infections |
title_full | Hemocytes and fat body cells, the only professional immune cell types in Drosophila, show strikingly different responses to systemic infections |
title_fullStr | Hemocytes and fat body cells, the only professional immune cell types in Drosophila, show strikingly different responses to systemic infections |
title_full_unstemmed | Hemocytes and fat body cells, the only professional immune cell types in Drosophila, show strikingly different responses to systemic infections |
title_short | Hemocytes and fat body cells, the only professional immune cell types in Drosophila, show strikingly different responses to systemic infections |
title_sort | hemocytes and fat body cells, the only professional immune cell types in drosophila, show strikingly different responses to systemic infections |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9726733/ https://www.ncbi.nlm.nih.gov/pubmed/36505446 http://dx.doi.org/10.3389/fimmu.2022.1040510 |
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