Cargando…

Drosophila larval to pupal switch under nutrient stress requires IP(3)R/Ca(2+) signalling in glutamatergic interneurons

Neuronal circuits are known to integrate nutritional information, but the identity of the circuit components is not completely understood. Amino acids are a class of nutrients that are vital for the growth and function of an organism. Here, we report a neuronal circuit that allows Drosophila larvae...

Descripción completa

Detalles Bibliográficos
Autores principales: Jayakumar, Siddharth, Richhariya, Shlesha, Reddy, O Venkateswara, Texada, Michael J, Hasan, Gaiti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993588/
https://www.ncbi.nlm.nih.gov/pubmed/27494275
http://dx.doi.org/10.7554/eLife.17495
_version_ 1782449171862650880
author Jayakumar, Siddharth
Richhariya, Shlesha
Reddy, O Venkateswara
Texada, Michael J
Hasan, Gaiti
author_facet Jayakumar, Siddharth
Richhariya, Shlesha
Reddy, O Venkateswara
Texada, Michael J
Hasan, Gaiti
author_sort Jayakumar, Siddharth
collection PubMed
description Neuronal circuits are known to integrate nutritional information, but the identity of the circuit components is not completely understood. Amino acids are a class of nutrients that are vital for the growth and function of an organism. Here, we report a neuronal circuit that allows Drosophila larvae to overcome amino acid deprivation and pupariate. We find that nutrient stress is sensed by the class IV multidendritic cholinergic neurons. Through live calcium imaging experiments, we show that these cholinergic stimuli are conveyed to glutamatergic neurons in the ventral ganglion through mAChR. We further show that IP(3)R-dependent calcium transients in the glutamatergic neurons convey this signal to downstream medial neurosecretory cells (mNSCs). The circuit ultimately converges at the ring gland and regulates expression of ecdysteroid biosynthetic genes. Activity in this circuit is thus likely to be an adaptation that provides a layer of regulation to help surpass nutritional stress during development. DOI: http://dx.doi.org/10.7554/eLife.17495.001
format Online
Article
Text
id pubmed-4993588
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-49935882016-08-24 Drosophila larval to pupal switch under nutrient stress requires IP(3)R/Ca(2+) signalling in glutamatergic interneurons Jayakumar, Siddharth Richhariya, Shlesha Reddy, O Venkateswara Texada, Michael J Hasan, Gaiti eLife Neuroscience Neuronal circuits are known to integrate nutritional information, but the identity of the circuit components is not completely understood. Amino acids are a class of nutrients that are vital for the growth and function of an organism. Here, we report a neuronal circuit that allows Drosophila larvae to overcome amino acid deprivation and pupariate. We find that nutrient stress is sensed by the class IV multidendritic cholinergic neurons. Through live calcium imaging experiments, we show that these cholinergic stimuli are conveyed to glutamatergic neurons in the ventral ganglion through mAChR. We further show that IP(3)R-dependent calcium transients in the glutamatergic neurons convey this signal to downstream medial neurosecretory cells (mNSCs). The circuit ultimately converges at the ring gland and regulates expression of ecdysteroid biosynthetic genes. Activity in this circuit is thus likely to be an adaptation that provides a layer of regulation to help surpass nutritional stress during development. DOI: http://dx.doi.org/10.7554/eLife.17495.001 eLife Sciences Publications, Ltd 2016-08-05 /pmc/articles/PMC4993588/ /pubmed/27494275 http://dx.doi.org/10.7554/eLife.17495 Text en © 2016, Jayakumar et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Jayakumar, Siddharth
Richhariya, Shlesha
Reddy, O Venkateswara
Texada, Michael J
Hasan, Gaiti
Drosophila larval to pupal switch under nutrient stress requires IP(3)R/Ca(2+) signalling in glutamatergic interneurons
title Drosophila larval to pupal switch under nutrient stress requires IP(3)R/Ca(2+) signalling in glutamatergic interneurons
title_full Drosophila larval to pupal switch under nutrient stress requires IP(3)R/Ca(2+) signalling in glutamatergic interneurons
title_fullStr Drosophila larval to pupal switch under nutrient stress requires IP(3)R/Ca(2+) signalling in glutamatergic interneurons
title_full_unstemmed Drosophila larval to pupal switch under nutrient stress requires IP(3)R/Ca(2+) signalling in glutamatergic interneurons
title_short Drosophila larval to pupal switch under nutrient stress requires IP(3)R/Ca(2+) signalling in glutamatergic interneurons
title_sort drosophila larval to pupal switch under nutrient stress requires ip(3)r/ca(2+) signalling in glutamatergic interneurons
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993588/
https://www.ncbi.nlm.nih.gov/pubmed/27494275
http://dx.doi.org/10.7554/eLife.17495
work_keys_str_mv AT jayakumarsiddharth drosophilalarvaltopupalswitchundernutrientstressrequiresip3rca2signallinginglutamatergicinterneurons
AT richhariyashlesha drosophilalarvaltopupalswitchundernutrientstressrequiresip3rca2signallinginglutamatergicinterneurons
AT reddyovenkateswara drosophilalarvaltopupalswitchundernutrientstressrequiresip3rca2signallinginglutamatergicinterneurons
AT texadamichaelj drosophilalarvaltopupalswitchundernutrientstressrequiresip3rca2signallinginglutamatergicinterneurons
AT hasangaiti drosophilalarvaltopupalswitchundernutrientstressrequiresip3rca2signallinginglutamatergicinterneurons