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An intestinal sphingolipid confers intergenerational neuroprotection

In animals, maternal diet and environment can influence the health of offspring. Whether and how maternal dietary choice impacts the nervous system across multiple generations is not well understood. Here we show that feeding Caenorhabditis elegans with ursolic acid, a natural plant product, improve...

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Autores principales: Wang, Wenyue, Sherry, Tessa, Cheng, Xinran, Fan, Qi, Cornell, Rebecca, Liu, Jie, Xiao, Zhicheng, Pocock, Roger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415181/
https://www.ncbi.nlm.nih.gov/pubmed/37537365
http://dx.doi.org/10.1038/s41556-023-01195-9
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author Wang, Wenyue
Sherry, Tessa
Cheng, Xinran
Fan, Qi
Cornell, Rebecca
Liu, Jie
Xiao, Zhicheng
Pocock, Roger
author_facet Wang, Wenyue
Sherry, Tessa
Cheng, Xinran
Fan, Qi
Cornell, Rebecca
Liu, Jie
Xiao, Zhicheng
Pocock, Roger
author_sort Wang, Wenyue
collection PubMed
description In animals, maternal diet and environment can influence the health of offspring. Whether and how maternal dietary choice impacts the nervous system across multiple generations is not well understood. Here we show that feeding Caenorhabditis elegans with ursolic acid, a natural plant product, improves axon transport and reduces adult-onset axon fragility intergenerationally. Ursolic acid provides neuroprotection by enhancing maternal provisioning of sphingosine-1-phosphate, a bioactive sphingolipid. Intestine-to-oocyte sphingosine-1-phosphate transfer is required for intergenerational neuroprotection and is dependent on the RME-2 lipoprotein yolk receptor. Sphingosine-1-phosphate acts intergenerationally by upregulating the transcription of the acid ceramidase-1 (asah-1) gene in the intestine. Spatial regulation of sphingolipid metabolism is critical, as inappropriate asah-1 expression in neurons causes developmental axon outgrowth defects. Our results show that sphingolipid homeostasis impacts the development and intergenerational health of the nervous system. The ability of specific lipid metabolites to act as messengers between generations may have broad implications for dietary choice during reproduction.
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spelling pubmed-104151812023-08-12 An intestinal sphingolipid confers intergenerational neuroprotection Wang, Wenyue Sherry, Tessa Cheng, Xinran Fan, Qi Cornell, Rebecca Liu, Jie Xiao, Zhicheng Pocock, Roger Nat Cell Biol Article In animals, maternal diet and environment can influence the health of offspring. Whether and how maternal dietary choice impacts the nervous system across multiple generations is not well understood. Here we show that feeding Caenorhabditis elegans with ursolic acid, a natural plant product, improves axon transport and reduces adult-onset axon fragility intergenerationally. Ursolic acid provides neuroprotection by enhancing maternal provisioning of sphingosine-1-phosphate, a bioactive sphingolipid. Intestine-to-oocyte sphingosine-1-phosphate transfer is required for intergenerational neuroprotection and is dependent on the RME-2 lipoprotein yolk receptor. Sphingosine-1-phosphate acts intergenerationally by upregulating the transcription of the acid ceramidase-1 (asah-1) gene in the intestine. Spatial regulation of sphingolipid metabolism is critical, as inappropriate asah-1 expression in neurons causes developmental axon outgrowth defects. Our results show that sphingolipid homeostasis impacts the development and intergenerational health of the nervous system. The ability of specific lipid metabolites to act as messengers between generations may have broad implications for dietary choice during reproduction. Nature Publishing Group UK 2023-08-03 2023 /pmc/articles/PMC10415181/ /pubmed/37537365 http://dx.doi.org/10.1038/s41556-023-01195-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Wenyue
Sherry, Tessa
Cheng, Xinran
Fan, Qi
Cornell, Rebecca
Liu, Jie
Xiao, Zhicheng
Pocock, Roger
An intestinal sphingolipid confers intergenerational neuroprotection
title An intestinal sphingolipid confers intergenerational neuroprotection
title_full An intestinal sphingolipid confers intergenerational neuroprotection
title_fullStr An intestinal sphingolipid confers intergenerational neuroprotection
title_full_unstemmed An intestinal sphingolipid confers intergenerational neuroprotection
title_short An intestinal sphingolipid confers intergenerational neuroprotection
title_sort intestinal sphingolipid confers intergenerational neuroprotection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415181/
https://www.ncbi.nlm.nih.gov/pubmed/37537365
http://dx.doi.org/10.1038/s41556-023-01195-9
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