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Neuronal Control of Metabolism through Nutrient-Dependent Modulation of Tracheal Branching
During adaptive angiogenesis, a key process in the etiology and treatment of cancer and obesity, the vasculature changes to meet the metabolic needs of its target tissues. Although the cues governing vascular remodeling are not fully understood, target-derived signals are generally believed to under...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898607/ https://www.ncbi.nlm.nih.gov/pubmed/24439370 http://dx.doi.org/10.1016/j.cell.2013.12.008 |
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author | Linneweber, Gerit A. Jacobson, Jake Busch, Karl Emanuel Hudry, Bruno Christov, Christo P. Dormann, Dirk Yuan, Michaela Otani, Tomoki Knust, Elisabeth de Bono, Mario Miguel-Aliaga, Irene |
author_facet | Linneweber, Gerit A. Jacobson, Jake Busch, Karl Emanuel Hudry, Bruno Christov, Christo P. Dormann, Dirk Yuan, Michaela Otani, Tomoki Knust, Elisabeth de Bono, Mario Miguel-Aliaga, Irene |
author_sort | Linneweber, Gerit A. |
collection | PubMed |
description | During adaptive angiogenesis, a key process in the etiology and treatment of cancer and obesity, the vasculature changes to meet the metabolic needs of its target tissues. Although the cues governing vascular remodeling are not fully understood, target-derived signals are generally believed to underlie this process. Here, we identify an alternative mechanism by characterizing the previously unrecognized nutrient-dependent plasticity of the Drosophila tracheal system: a network of oxygen-delivering tubules developmentally akin to mammalian blood vessels. We find that this plasticity, particularly prominent in the intestine, drives—rather than responds to—metabolic change. Mechanistically, it is regulated by distinct populations of nutrient- and oxygen-responsive neurons that, through delivery of both local and systemic insulin- and VIP-like neuropeptides, sculpt the growth of specific tracheal subsets. Thus, we describe a novel mechanism by which nutritional cues modulate neuronal activity to give rise to organ-specific, long-lasting changes in vascular architecture. |
format | Online Article Text |
id | pubmed-3898607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38986072014-01-24 Neuronal Control of Metabolism through Nutrient-Dependent Modulation of Tracheal Branching Linneweber, Gerit A. Jacobson, Jake Busch, Karl Emanuel Hudry, Bruno Christov, Christo P. Dormann, Dirk Yuan, Michaela Otani, Tomoki Knust, Elisabeth de Bono, Mario Miguel-Aliaga, Irene Cell Article During adaptive angiogenesis, a key process in the etiology and treatment of cancer and obesity, the vasculature changes to meet the metabolic needs of its target tissues. Although the cues governing vascular remodeling are not fully understood, target-derived signals are generally believed to underlie this process. Here, we identify an alternative mechanism by characterizing the previously unrecognized nutrient-dependent plasticity of the Drosophila tracheal system: a network of oxygen-delivering tubules developmentally akin to mammalian blood vessels. We find that this plasticity, particularly prominent in the intestine, drives—rather than responds to—metabolic change. Mechanistically, it is regulated by distinct populations of nutrient- and oxygen-responsive neurons that, through delivery of both local and systemic insulin- and VIP-like neuropeptides, sculpt the growth of specific tracheal subsets. Thus, we describe a novel mechanism by which nutritional cues modulate neuronal activity to give rise to organ-specific, long-lasting changes in vascular architecture. Cell Press 2014-01-16 /pmc/articles/PMC3898607/ /pubmed/24439370 http://dx.doi.org/10.1016/j.cell.2013.12.008 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Linneweber, Gerit A. Jacobson, Jake Busch, Karl Emanuel Hudry, Bruno Christov, Christo P. Dormann, Dirk Yuan, Michaela Otani, Tomoki Knust, Elisabeth de Bono, Mario Miguel-Aliaga, Irene Neuronal Control of Metabolism through Nutrient-Dependent Modulation of Tracheal Branching |
title | Neuronal Control of Metabolism through Nutrient-Dependent Modulation of Tracheal Branching |
title_full | Neuronal Control of Metabolism through Nutrient-Dependent Modulation of Tracheal Branching |
title_fullStr | Neuronal Control of Metabolism through Nutrient-Dependent Modulation of Tracheal Branching |
title_full_unstemmed | Neuronal Control of Metabolism through Nutrient-Dependent Modulation of Tracheal Branching |
title_short | Neuronal Control of Metabolism through Nutrient-Dependent Modulation of Tracheal Branching |
title_sort | neuronal control of metabolism through nutrient-dependent modulation of tracheal branching |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898607/ https://www.ncbi.nlm.nih.gov/pubmed/24439370 http://dx.doi.org/10.1016/j.cell.2013.12.008 |
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