Cargando…

Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism

Food intake and energy metabolism are tightly controlled to maintain stable energy homeostasis and healthy states. Thus, animals detect their stored energy levels, and based on this, they determine appropriate food intake and meal size. Drosophila melanogaster putative G protein-coupled receptor, Br...

Descripción completa

Detalles Bibliográficos
Autores principales: Kohyama-Koganeya, Ayako, Kurosawa, Mizuki, Hirabayashi, Yoshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508045/
https://www.ncbi.nlm.nih.gov/pubmed/26193363
http://dx.doi.org/10.1371/journal.pone.0133083
_version_ 1782381880388091904
author Kohyama-Koganeya, Ayako
Kurosawa, Mizuki
Hirabayashi, Yoshio
author_facet Kohyama-Koganeya, Ayako
Kurosawa, Mizuki
Hirabayashi, Yoshio
author_sort Kohyama-Koganeya, Ayako
collection PubMed
description Food intake and energy metabolism are tightly controlled to maintain stable energy homeostasis and healthy states. Thus, animals detect their stored energy levels, and based on this, they determine appropriate food intake and meal size. Drosophila melanogaster putative G protein-coupled receptor, Bride of sevenless (BOSS) is a highly evolutionarily conserved protein that responds to extracellular glucose levels in order to regulate energy homeostasis. To address how BOSS regulates energy homeostasis, we characterized a boss mutant by assessing its food intake and stored energy levels. Boss mutants exhibited increased food intake but decreased stored triacylglyceride levels. Using boss-GAL4 drivers, we found that boss is expressed in select tissues that are involved in nutrient sensing and food intake, in a subset of neurons in brain and chemosensory organs, in fat body, and in endocrine cells in gut (enteroendocrine cells). Flies with tissue-specific boss knockdowns in these tissues had abnormal stored energy levels and abnormal food intake. These results suggest that BOSS in either neurons or peripheral nutrient-sensing tissues affects energy homeostasis in ways that relate to the sensing of nutrients and regulation of food intake.
format Online
Article
Text
id pubmed-4508045
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-45080452015-07-24 Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism Kohyama-Koganeya, Ayako Kurosawa, Mizuki Hirabayashi, Yoshio PLoS One Research Article Food intake and energy metabolism are tightly controlled to maintain stable energy homeostasis and healthy states. Thus, animals detect their stored energy levels, and based on this, they determine appropriate food intake and meal size. Drosophila melanogaster putative G protein-coupled receptor, Bride of sevenless (BOSS) is a highly evolutionarily conserved protein that responds to extracellular glucose levels in order to regulate energy homeostasis. To address how BOSS regulates energy homeostasis, we characterized a boss mutant by assessing its food intake and stored energy levels. Boss mutants exhibited increased food intake but decreased stored triacylglyceride levels. Using boss-GAL4 drivers, we found that boss is expressed in select tissues that are involved in nutrient sensing and food intake, in a subset of neurons in brain and chemosensory organs, in fat body, and in endocrine cells in gut (enteroendocrine cells). Flies with tissue-specific boss knockdowns in these tissues had abnormal stored energy levels and abnormal food intake. These results suggest that BOSS in either neurons or peripheral nutrient-sensing tissues affects energy homeostasis in ways that relate to the sensing of nutrients and regulation of food intake. Public Library of Science 2015-07-20 /pmc/articles/PMC4508045/ /pubmed/26193363 http://dx.doi.org/10.1371/journal.pone.0133083 Text en © 2015 Kohyama-Koganeya 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
Kohyama-Koganeya, Ayako
Kurosawa, Mizuki
Hirabayashi, Yoshio
Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism
title Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism
title_full Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism
title_fullStr Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism
title_full_unstemmed Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism
title_short Differential Effects of Tissue-Specific Deletion of BOSS on Feeding Behaviors and Energy Metabolism
title_sort differential effects of tissue-specific deletion of boss on feeding behaviors and energy metabolism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508045/
https://www.ncbi.nlm.nih.gov/pubmed/26193363
http://dx.doi.org/10.1371/journal.pone.0133083
work_keys_str_mv AT kohyamakoganeyaayako differentialeffectsoftissuespecificdeletionofbossonfeedingbehaviorsandenergymetabolism
AT kurosawamizuki differentialeffectsoftissuespecificdeletionofbossonfeedingbehaviorsandenergymetabolism
AT hirabayashiyoshio differentialeffectsoftissuespecificdeletionofbossonfeedingbehaviorsandenergymetabolism