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ADrosophilagenetic model of nephrolithiasis: transcriptional changes in response to diet induced stone formation

BACKGROUND: Urolithiasis is a significant healthcare issue but the pathophysiology of stone disease remains poorly understood. Drosophila Malpighian tubules were known to share similar physiological function to human renal tubules. We have used Drosophila as a genetic model to study the transcriptio...

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Autores principales: Chung, Vera Y., Turney, Benjamin W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706311/
https://www.ncbi.nlm.nih.gov/pubmed/29183349
http://dx.doi.org/10.1186/s12894-017-0292-5
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author Chung, Vera Y.
Turney, Benjamin W.
author_facet Chung, Vera Y.
Turney, Benjamin W.
author_sort Chung, Vera Y.
collection PubMed
description BACKGROUND: Urolithiasis is a significant healthcare issue but the pathophysiology of stone disease remains poorly understood. Drosophila Malpighian tubules were known to share similar physiological function to human renal tubules. We have used Drosophila as a genetic model to study the transcriptional response to stone formation secondary to dietary manipulation. METHODS: Wild-type male flies were raised on standard medium supplemented with lithogenic agents: control, sodium oxalate (NaOx) and ethylene glycol (EG). At 2 weeks, Malpighian tubules were dissected under polarized microscope to visualize crystals. The parallel group was dissected for RNA extraction and subsequent next-generation RNA sequencing. RESULTS: Crystal formation was visualized in 20%(±2.2) of flies on control diet, 73%(±3.6) on NaOx diet and 84%(±2.2) on EG diet. Differentially expressed genes were identified in flies fed with NaOx and EG diet comparing with the control group. Fifty-eight genes were differentially expressed (FDR <0.05, p < 0.05) in NaOx diet and 20 genes in EG diet. The molecular function of differentially expressed genes were assessed. Among these, Nervana 3, Eaat1 (Excitatory amino acid transporter 1), CG7912, CG5404, CG3036 worked as ion transmembrane transporters, which were possibly involved in stone pathogenesis. CONCLUSIONS: We have shown that by dietary modification, stone formation can be manipulated and visualized in Drosophila Malpighian tubules. This genetic model could be potentially used to identify the candidate genes that influence stone risk hence providing more insight to the pathogenesis of human stone disease.
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spelling pubmed-57063112017-12-05 ADrosophilagenetic model of nephrolithiasis: transcriptional changes in response to diet induced stone formation Chung, Vera Y. Turney, Benjamin W. BMC Urol Research Article BACKGROUND: Urolithiasis is a significant healthcare issue but the pathophysiology of stone disease remains poorly understood. Drosophila Malpighian tubules were known to share similar physiological function to human renal tubules. We have used Drosophila as a genetic model to study the transcriptional response to stone formation secondary to dietary manipulation. METHODS: Wild-type male flies were raised on standard medium supplemented with lithogenic agents: control, sodium oxalate (NaOx) and ethylene glycol (EG). At 2 weeks, Malpighian tubules were dissected under polarized microscope to visualize crystals. The parallel group was dissected for RNA extraction and subsequent next-generation RNA sequencing. RESULTS: Crystal formation was visualized in 20%(±2.2) of flies on control diet, 73%(±3.6) on NaOx diet and 84%(±2.2) on EG diet. Differentially expressed genes were identified in flies fed with NaOx and EG diet comparing with the control group. Fifty-eight genes were differentially expressed (FDR <0.05, p < 0.05) in NaOx diet and 20 genes in EG diet. The molecular function of differentially expressed genes were assessed. Among these, Nervana 3, Eaat1 (Excitatory amino acid transporter 1), CG7912, CG5404, CG3036 worked as ion transmembrane transporters, which were possibly involved in stone pathogenesis. CONCLUSIONS: We have shown that by dietary modification, stone formation can be manipulated and visualized in Drosophila Malpighian tubules. This genetic model could be potentially used to identify the candidate genes that influence stone risk hence providing more insight to the pathogenesis of human stone disease. BioMed Central 2017-11-28 /pmc/articles/PMC5706311/ /pubmed/29183349 http://dx.doi.org/10.1186/s12894-017-0292-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chung, Vera Y.
Turney, Benjamin W.
ADrosophilagenetic model of nephrolithiasis: transcriptional changes in response to diet induced stone formation
title ADrosophilagenetic model of nephrolithiasis: transcriptional changes in response to diet induced stone formation
title_full ADrosophilagenetic model of nephrolithiasis: transcriptional changes in response to diet induced stone formation
title_fullStr ADrosophilagenetic model of nephrolithiasis: transcriptional changes in response to diet induced stone formation
title_full_unstemmed ADrosophilagenetic model of nephrolithiasis: transcriptional changes in response to diet induced stone formation
title_short ADrosophilagenetic model of nephrolithiasis: transcriptional changes in response to diet induced stone formation
title_sort adrosophilagenetic model of nephrolithiasis: transcriptional changes in response to diet induced stone formation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706311/
https://www.ncbi.nlm.nih.gov/pubmed/29183349
http://dx.doi.org/10.1186/s12894-017-0292-5
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