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Adult Drosophila melanogaster as a model for the study of glucose homeostasis

Genetic ablation of Drosophila melanogaster insulin-like peptide (DILP) and adipokinetic hormone-producing cells accompanied by cell biological and metabolic measurements have revealed functional conservation in nutrient sensing and the underlying signaling mechanisms between mammal and fruit fly. D...

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Autores principales: Haselton, Aaron T., Fridell, Yih-Woei C.
Formato: Texto
Lenguaje:English
Publicado: Impact Journals LLC 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954044/
https://www.ncbi.nlm.nih.gov/pubmed/20689157
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author Haselton, Aaron T.
Fridell, Yih-Woei C.
author_facet Haselton, Aaron T.
Fridell, Yih-Woei C.
author_sort Haselton, Aaron T.
collection PubMed
description Genetic ablation of Drosophila melanogaster insulin-like peptide (DILP) and adipokinetic hormone-producing cells accompanied by cell biological and metabolic measurements have revealed functional conservation in nutrient sensing and the underlying signaling mechanisms between mammal and fruit fly. Despite significant advances gained in understanding the neuroendocrine responses to nutrient changes during developmental larval stages, we discuss here the need for investigating glucose homeostasis in the post-mitotic adult stage as the result of ablation of DILP producing cells (IPCs). Our recent studies demonstrate that while both constitutive and adult-specific partial ablation of IPCs renders those flies hyperglycemic and glucose intolerant, flies with adult-specific IPC ablation remain insulin sensitive. Our results substantiate a role of adult IPCs in modulating aspects of glucose homeostasis and highlight the complexity in DILP action in the adult fly.
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spelling pubmed-29540442010-10-14 Adult Drosophila melanogaster as a model for the study of glucose homeostasis Haselton, Aaron T. Fridell, Yih-Woei C. Aging (Albany NY) Research Perspective Genetic ablation of Drosophila melanogaster insulin-like peptide (DILP) and adipokinetic hormone-producing cells accompanied by cell biological and metabolic measurements have revealed functional conservation in nutrient sensing and the underlying signaling mechanisms between mammal and fruit fly. Despite significant advances gained in understanding the neuroendocrine responses to nutrient changes during developmental larval stages, we discuss here the need for investigating glucose homeostasis in the post-mitotic adult stage as the result of ablation of DILP producing cells (IPCs). Our recent studies demonstrate that while both constitutive and adult-specific partial ablation of IPCs renders those flies hyperglycemic and glucose intolerant, flies with adult-specific IPC ablation remain insulin sensitive. Our results substantiate a role of adult IPCs in modulating aspects of glucose homeostasis and highlight the complexity in DILP action in the adult fly. Impact Journals LLC 2010-08-05 /pmc/articles/PMC2954044/ /pubmed/20689157 Text en Copyright: ©2010 Haselton et al. http://creativecommons.org/licenses/by/2.5/ 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 work is properly cited.
spellingShingle Research Perspective
Haselton, Aaron T.
Fridell, Yih-Woei C.
Adult Drosophila melanogaster as a model for the study of glucose homeostasis
title Adult Drosophila melanogaster as a model for the study of glucose homeostasis
title_full Adult Drosophila melanogaster as a model for the study of glucose homeostasis
title_fullStr Adult Drosophila melanogaster as a model for the study of glucose homeostasis
title_full_unstemmed Adult Drosophila melanogaster as a model for the study of glucose homeostasis
title_short Adult Drosophila melanogaster as a model for the study of glucose homeostasis
title_sort adult drosophila melanogaster as a model for the study of glucose homeostasis
topic Research Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954044/
https://www.ncbi.nlm.nih.gov/pubmed/20689157
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