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Grandpaternal-induced transgenerational dietary reprogramming of the unfolded protein response in skeletal muscle

OBJECTIVE: Parental nutrition and lifestyle impact the metabolic phenotype of the offspring. We have reported that grandpaternal chronic high-fat diet (HFD) transgenerationally impairs glucose metabolism in subsequent generations. Here we determined whether grandpaternal diet transgenerationally imp...

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Autores principales: Alm, Petter S., de Castro Barbosa, Thais, Barrès, Romain, Krook, Anna, Zierath, Juleen R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485306/
https://www.ncbi.nlm.nih.gov/pubmed/28702319
http://dx.doi.org/10.1016/j.molmet.2017.05.009
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author Alm, Petter S.
de Castro Barbosa, Thais
Barrès, Romain
Krook, Anna
Zierath, Juleen R.
author_facet Alm, Petter S.
de Castro Barbosa, Thais
Barrès, Romain
Krook, Anna
Zierath, Juleen R.
author_sort Alm, Petter S.
collection PubMed
description OBJECTIVE: Parental nutrition and lifestyle impact the metabolic phenotype of the offspring. We have reported that grandpaternal chronic high-fat diet (HFD) transgenerationally impairs glucose metabolism in subsequent generations. Here we determined whether grandpaternal diet transgenerationally impacts the transcriptome and lipidome in skeletal muscle. Our aim was to identify tissue-specific pathways involved in transgenerational inheritance of environmental-induced phenotypes. METHODS: F0 male Sprague–Dawley rats were fed a HFD or chow for 12 weeks before breeding with chow-fed females to generate the F1 generation. F2 offspring were generated by mating F1 males fed a chow diet with an independent line of chow-fed females. F1 and F2 offspring were fed chow or HFD for 12 weeks. Transcriptomic and LC-MS lipidomic analyses were performed in extensor digitorum longus muscle from F2-females rats. Gene set enrichment analysis (GSEA) was performed to determine pathways reprogrammed by grandpaternal diet. RESULTS: GSEA revealed an enrichment of the unfolded protein response pathway in skeletal muscle of grand-offspring from HFD-fed grandfathers compared to grand-offspring of chow-fed males. Activation of the stress sensor (ATF6α), may be a pivotal point whereby this pathway is activated. Interestingly, skeletal muscle from F1-offspring was not affected in a similar manner. No major changes were observed in the skeletal muscle lipidome profile due to grandpaternal diet. CONCLUSIONS: Grandpaternal HFD-induced obesity transgenerationally affected the skeletal muscle transcriptome. This finding further highlights the impact of parental exposure to environmental factors on offspring's development and health.
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spelling pubmed-54853062017-07-12 Grandpaternal-induced transgenerational dietary reprogramming of the unfolded protein response in skeletal muscle Alm, Petter S. de Castro Barbosa, Thais Barrès, Romain Krook, Anna Zierath, Juleen R. Mol Metab Original Article OBJECTIVE: Parental nutrition and lifestyle impact the metabolic phenotype of the offspring. We have reported that grandpaternal chronic high-fat diet (HFD) transgenerationally impairs glucose metabolism in subsequent generations. Here we determined whether grandpaternal diet transgenerationally impacts the transcriptome and lipidome in skeletal muscle. Our aim was to identify tissue-specific pathways involved in transgenerational inheritance of environmental-induced phenotypes. METHODS: F0 male Sprague–Dawley rats were fed a HFD or chow for 12 weeks before breeding with chow-fed females to generate the F1 generation. F2 offspring were generated by mating F1 males fed a chow diet with an independent line of chow-fed females. F1 and F2 offspring were fed chow or HFD for 12 weeks. Transcriptomic and LC-MS lipidomic analyses were performed in extensor digitorum longus muscle from F2-females rats. Gene set enrichment analysis (GSEA) was performed to determine pathways reprogrammed by grandpaternal diet. RESULTS: GSEA revealed an enrichment of the unfolded protein response pathway in skeletal muscle of grand-offspring from HFD-fed grandfathers compared to grand-offspring of chow-fed males. Activation of the stress sensor (ATF6α), may be a pivotal point whereby this pathway is activated. Interestingly, skeletal muscle from F1-offspring was not affected in a similar manner. No major changes were observed in the skeletal muscle lipidome profile due to grandpaternal diet. CONCLUSIONS: Grandpaternal HFD-induced obesity transgenerationally affected the skeletal muscle transcriptome. This finding further highlights the impact of parental exposure to environmental factors on offspring's development and health. Elsevier 2017-05-22 /pmc/articles/PMC5485306/ /pubmed/28702319 http://dx.doi.org/10.1016/j.molmet.2017.05.009 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Alm, Petter S.
de Castro Barbosa, Thais
Barrès, Romain
Krook, Anna
Zierath, Juleen R.
Grandpaternal-induced transgenerational dietary reprogramming of the unfolded protein response in skeletal muscle
title Grandpaternal-induced transgenerational dietary reprogramming of the unfolded protein response in skeletal muscle
title_full Grandpaternal-induced transgenerational dietary reprogramming of the unfolded protein response in skeletal muscle
title_fullStr Grandpaternal-induced transgenerational dietary reprogramming of the unfolded protein response in skeletal muscle
title_full_unstemmed Grandpaternal-induced transgenerational dietary reprogramming of the unfolded protein response in skeletal muscle
title_short Grandpaternal-induced transgenerational dietary reprogramming of the unfolded protein response in skeletal muscle
title_sort grandpaternal-induced transgenerational dietary reprogramming of the unfolded protein response in skeletal muscle
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485306/
https://www.ncbi.nlm.nih.gov/pubmed/28702319
http://dx.doi.org/10.1016/j.molmet.2017.05.009
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