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Metabolic memory of Δ9-tetrahydrocannabinol exposure in pluripotent stem cells and primordial germ cells-like cells

Cannabis, the most consumed illicit psychoactive drug in the world, is increasingly used by pregnant women. However, while cannabinoid receptors are expressed in the early embryo, the impact of phytocannabinoids exposure on early embryonic processes is lacking. Here, we leverage a stepwise in vitro...

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Autores principales: Verdikt, Roxane, Armstrong, Abigail A., Cheng, Jenny, Hwang, Young Sun, Clark, Amander T., Yang, Xia, Allard, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054962/
https://www.ncbi.nlm.nih.gov/pubmed/36993751
http://dx.doi.org/10.1101/2023.03.13.531968
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author Verdikt, Roxane
Armstrong, Abigail A.
Cheng, Jenny
Hwang, Young Sun
Clark, Amander T.
Yang, Xia
Allard, Patrick
author_facet Verdikt, Roxane
Armstrong, Abigail A.
Cheng, Jenny
Hwang, Young Sun
Clark, Amander T.
Yang, Xia
Allard, Patrick
author_sort Verdikt, Roxane
collection PubMed
description Cannabis, the most consumed illicit psychoactive drug in the world, is increasingly used by pregnant women. However, while cannabinoid receptors are expressed in the early embryo, the impact of phytocannabinoids exposure on early embryonic processes is lacking. Here, we leverage a stepwise in vitro differentiation system that captures early embryonic developmental cascade to investigate the impact of exposure to the most abundant phytocannabinoid, Δ9-tetrahydrocannabinol (Δ9-THC). We demonstrate that Δ9-THC increases the proliferation of naïve mouse embryonic stem cells (ESCs) but not of their primed counterpart. Surprisingly, this increased proliferation, dependent on the CB1 receptor binding, is only associated with moderate transcriptomic changes. Instead, Δ9-THC capitalizes on ESCs’ metabolic bivalence by increasing their glycolytic rates and anabolic capabilities. A memory of this metabolic rewiring is retained throughout differentiation to Primordial Germ Cell-Like Cells in the absence of direct exposure and is associated with an alteration of their transcriptional profile. These results represent the first in-depth molecular characterization of the impact of Δ9-THC exposure on early stages of germline development.
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spelling pubmed-100549622023-03-30 Metabolic memory of Δ9-tetrahydrocannabinol exposure in pluripotent stem cells and primordial germ cells-like cells Verdikt, Roxane Armstrong, Abigail A. Cheng, Jenny Hwang, Young Sun Clark, Amander T. Yang, Xia Allard, Patrick bioRxiv Article Cannabis, the most consumed illicit psychoactive drug in the world, is increasingly used by pregnant women. However, while cannabinoid receptors are expressed in the early embryo, the impact of phytocannabinoids exposure on early embryonic processes is lacking. Here, we leverage a stepwise in vitro differentiation system that captures early embryonic developmental cascade to investigate the impact of exposure to the most abundant phytocannabinoid, Δ9-tetrahydrocannabinol (Δ9-THC). We demonstrate that Δ9-THC increases the proliferation of naïve mouse embryonic stem cells (ESCs) but not of their primed counterpart. Surprisingly, this increased proliferation, dependent on the CB1 receptor binding, is only associated with moderate transcriptomic changes. Instead, Δ9-THC capitalizes on ESCs’ metabolic bivalence by increasing their glycolytic rates and anabolic capabilities. A memory of this metabolic rewiring is retained throughout differentiation to Primordial Germ Cell-Like Cells in the absence of direct exposure and is associated with an alteration of their transcriptional profile. These results represent the first in-depth molecular characterization of the impact of Δ9-THC exposure on early stages of germline development. Cold Spring Harbor Laboratory 2023-10-02 /pmc/articles/PMC10054962/ /pubmed/36993751 http://dx.doi.org/10.1101/2023.03.13.531968 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Verdikt, Roxane
Armstrong, Abigail A.
Cheng, Jenny
Hwang, Young Sun
Clark, Amander T.
Yang, Xia
Allard, Patrick
Metabolic memory of Δ9-tetrahydrocannabinol exposure in pluripotent stem cells and primordial germ cells-like cells
title Metabolic memory of Δ9-tetrahydrocannabinol exposure in pluripotent stem cells and primordial germ cells-like cells
title_full Metabolic memory of Δ9-tetrahydrocannabinol exposure in pluripotent stem cells and primordial germ cells-like cells
title_fullStr Metabolic memory of Δ9-tetrahydrocannabinol exposure in pluripotent stem cells and primordial germ cells-like cells
title_full_unstemmed Metabolic memory of Δ9-tetrahydrocannabinol exposure in pluripotent stem cells and primordial germ cells-like cells
title_short Metabolic memory of Δ9-tetrahydrocannabinol exposure in pluripotent stem cells and primordial germ cells-like cells
title_sort metabolic memory of δ9-tetrahydrocannabinol exposure in pluripotent stem cells and primordial germ cells-like cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054962/
https://www.ncbi.nlm.nih.gov/pubmed/36993751
http://dx.doi.org/10.1101/2023.03.13.531968
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