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The Hemolymph Proteome of Fed and Starved Drosophila Larvae

The co-operation of specialized organ systems in complex multicellular organisms depends on effective chemical communication. Thus, body fluids (like blood, lymph or intraspinal fluid) contain myriads of signaling mediators apart from metabolites. Moreover, these fluids are also of crucial importanc...

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Autores principales: Handke, Björn, Poernbacher, Ingrid, Goetze, Sandra, Ahrens, Christian H., Omasits, Ulrich, Marty, Florian, Simigdala, Nikiana, Meyer, Imke, Wollscheid, Bernd, Brunner, Erich, Hafen, Ernst, Lehner, Christian F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3688620/
https://www.ncbi.nlm.nih.gov/pubmed/23840627
http://dx.doi.org/10.1371/journal.pone.0067208
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author Handke, Björn
Poernbacher, Ingrid
Goetze, Sandra
Ahrens, Christian H.
Omasits, Ulrich
Marty, Florian
Simigdala, Nikiana
Meyer, Imke
Wollscheid, Bernd
Brunner, Erich
Hafen, Ernst
Lehner, Christian F.
author_facet Handke, Björn
Poernbacher, Ingrid
Goetze, Sandra
Ahrens, Christian H.
Omasits, Ulrich
Marty, Florian
Simigdala, Nikiana
Meyer, Imke
Wollscheid, Bernd
Brunner, Erich
Hafen, Ernst
Lehner, Christian F.
author_sort Handke, Björn
collection PubMed
description The co-operation of specialized organ systems in complex multicellular organisms depends on effective chemical communication. Thus, body fluids (like blood, lymph or intraspinal fluid) contain myriads of signaling mediators apart from metabolites. Moreover, these fluids are also of crucial importance for immune and wound responses. Compositional analyses of human body fluids are therefore of paramount diagnostic importance. Further improving their comprehensiveness should increase our understanding of inter-organ communication. In arthropods, which have trachea for gas exchange and an open circulatory system, the single dominating interstitial fluid is the hemolymph. Accordingly, a detailed analysis of hemolymph composition should provide an especially comprehensive picture of chemical communication and defense in animals. Therefore we used an extensive protein fractionation workflow in combination with a discovery-driven proteomic approach to map out the detectable protein composition of hemolymph isolated from Drosophila larvae. Combined mass spectrometric analysis revealed more than 700 proteins extending far beyond the previously known Drosophila hemolymph proteome. Moreover, by comparing hemolymph isolated from either fed or starved larvae, we provide initial provisional insights concerning compositional changes in response to nutritional state. Storage proteins in particular were observed to be strongly reduced by starvation. Our hemolymph proteome catalog provides a rich basis for data mining, as exemplified by our identification of potential novel cytokines, as well as for future quantitative analyses by targeted proteomics.
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spelling pubmed-36886202013-07-09 The Hemolymph Proteome of Fed and Starved Drosophila Larvae Handke, Björn Poernbacher, Ingrid Goetze, Sandra Ahrens, Christian H. Omasits, Ulrich Marty, Florian Simigdala, Nikiana Meyer, Imke Wollscheid, Bernd Brunner, Erich Hafen, Ernst Lehner, Christian F. PLoS One Research Article The co-operation of specialized organ systems in complex multicellular organisms depends on effective chemical communication. Thus, body fluids (like blood, lymph or intraspinal fluid) contain myriads of signaling mediators apart from metabolites. Moreover, these fluids are also of crucial importance for immune and wound responses. Compositional analyses of human body fluids are therefore of paramount diagnostic importance. Further improving their comprehensiveness should increase our understanding of inter-organ communication. In arthropods, which have trachea for gas exchange and an open circulatory system, the single dominating interstitial fluid is the hemolymph. Accordingly, a detailed analysis of hemolymph composition should provide an especially comprehensive picture of chemical communication and defense in animals. Therefore we used an extensive protein fractionation workflow in combination with a discovery-driven proteomic approach to map out the detectable protein composition of hemolymph isolated from Drosophila larvae. Combined mass spectrometric analysis revealed more than 700 proteins extending far beyond the previously known Drosophila hemolymph proteome. Moreover, by comparing hemolymph isolated from either fed or starved larvae, we provide initial provisional insights concerning compositional changes in response to nutritional state. Storage proteins in particular were observed to be strongly reduced by starvation. Our hemolymph proteome catalog provides a rich basis for data mining, as exemplified by our identification of potential novel cytokines, as well as for future quantitative analyses by targeted proteomics. Public Library of Science 2013-06-20 /pmc/articles/PMC3688620/ /pubmed/23840627 http://dx.doi.org/10.1371/journal.pone.0067208 Text en © 2013 Handke 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
Handke, Björn
Poernbacher, Ingrid
Goetze, Sandra
Ahrens, Christian H.
Omasits, Ulrich
Marty, Florian
Simigdala, Nikiana
Meyer, Imke
Wollscheid, Bernd
Brunner, Erich
Hafen, Ernst
Lehner, Christian F.
The Hemolymph Proteome of Fed and Starved Drosophila Larvae
title The Hemolymph Proteome of Fed and Starved Drosophila Larvae
title_full The Hemolymph Proteome of Fed and Starved Drosophila Larvae
title_fullStr The Hemolymph Proteome of Fed and Starved Drosophila Larvae
title_full_unstemmed The Hemolymph Proteome of Fed and Starved Drosophila Larvae
title_short The Hemolymph Proteome of Fed and Starved Drosophila Larvae
title_sort hemolymph proteome of fed and starved drosophila larvae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3688620/
https://www.ncbi.nlm.nih.gov/pubmed/23840627
http://dx.doi.org/10.1371/journal.pone.0067208
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