DHA but not EPA induces the trans-differentiation of C2C12 cells into white-like adipocytes phenotype.

Muscle derived stem cells (MDSCs) and myoblast play an important role in myotube regeneration when muscle tissue is injured. However, these cells can be induced to differentiate into adipocytes once exposed to PPARγ activator like EPA and DHA that are highly suggested during pregnancy. The objective...

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Autores principales: Saeed Ghnaimawi, Lisa Rebello, Jamie Baum, Yan Huang
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Publicado: Public Library of Science (PLoS) 2021
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Acceso en línea:https://doaj.org/article/f1c5ee6965fd4c52a17c0cac329f1279
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spelling oai:doaj.org-article:f1c5ee6965fd4c52a17c0cac329f12792021-12-02T20:08:39ZDHA but not EPA induces the trans-differentiation of C2C12 cells into white-like adipocytes phenotype.1932-620310.1371/journal.pone.0249438https://doaj.org/article/f1c5ee6965fd4c52a17c0cac329f12792021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0249438https://doaj.org/toc/1932-6203Muscle derived stem cells (MDSCs) and myoblast play an important role in myotube regeneration when muscle tissue is injured. However, these cells can be induced to differentiate into adipocytes once exposed to PPARγ activator like EPA and DHA that are highly suggested during pregnancy. The objective of this study aims at determining the identity of trans-differentiated cells by exploring the effect of EPA and DHA on C2C12 undergoing differentiation into brown and white adipocytes. DHA but not EPA committed C2C12 cells reprograming into white like adipocyte phenotype. Also, DHA promoted the expression of lipolysis regulating genes but had no effect on genes regulating β-oxidation referring to its implication in lipid re-esterification. Furthermore, DHA impaired C2C12 cells differentiation into brown adipocytes through reducing the thermogenic capacity and mitochondrial biogenesis of derived cells independent of UCP1. Accordingly, DHA treated groups showed an increased accumulation of lipid droplets and suppressed mitochondrial maximal respiration and spare respiratory capacity. EPA, on the other hand, reduced myogenesis regulating genes, but no significant differences were observed in the expression of adipogenesis key genes. Likewise, EPA suppressed the expression of WAT signature genes indicating that EPA and DHA have an independent role on white adipogensis. Unlike DHA treatment, EPA supplementation had no effect on the differential of C2C12 cells into brown adipocytes. In conclusion, DHA is a potent adipogenic and lipogenic factor that can change the metabolic profile of muscle cells by increasing myocellular fat.Saeed GhnaimawiLisa RebelloJamie BaumYan HuangPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 9, p e0249438 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Saeed Ghnaimawi
Lisa Rebello
Jamie Baum
Yan Huang
DHA but not EPA induces the trans-differentiation of C2C12 cells into white-like adipocytes phenotype.
description Muscle derived stem cells (MDSCs) and myoblast play an important role in myotube regeneration when muscle tissue is injured. However, these cells can be induced to differentiate into adipocytes once exposed to PPARγ activator like EPA and DHA that are highly suggested during pregnancy. The objective of this study aims at determining the identity of trans-differentiated cells by exploring the effect of EPA and DHA on C2C12 undergoing differentiation into brown and white adipocytes. DHA but not EPA committed C2C12 cells reprograming into white like adipocyte phenotype. Also, DHA promoted the expression of lipolysis regulating genes but had no effect on genes regulating β-oxidation referring to its implication in lipid re-esterification. Furthermore, DHA impaired C2C12 cells differentiation into brown adipocytes through reducing the thermogenic capacity and mitochondrial biogenesis of derived cells independent of UCP1. Accordingly, DHA treated groups showed an increased accumulation of lipid droplets and suppressed mitochondrial maximal respiration and spare respiratory capacity. EPA, on the other hand, reduced myogenesis regulating genes, but no significant differences were observed in the expression of adipogenesis key genes. Likewise, EPA suppressed the expression of WAT signature genes indicating that EPA and DHA have an independent role on white adipogensis. Unlike DHA treatment, EPA supplementation had no effect on the differential of C2C12 cells into brown adipocytes. In conclusion, DHA is a potent adipogenic and lipogenic factor that can change the metabolic profile of muscle cells by increasing myocellular fat.
format article
author Saeed Ghnaimawi
Lisa Rebello
Jamie Baum
Yan Huang
author_facet Saeed Ghnaimawi
Lisa Rebello
Jamie Baum
Yan Huang
author_sort Saeed Ghnaimawi
title DHA but not EPA induces the trans-differentiation of C2C12 cells into white-like adipocytes phenotype.
title_short DHA but not EPA induces the trans-differentiation of C2C12 cells into white-like adipocytes phenotype.
title_full DHA but not EPA induces the trans-differentiation of C2C12 cells into white-like adipocytes phenotype.
title_fullStr DHA but not EPA induces the trans-differentiation of C2C12 cells into white-like adipocytes phenotype.
title_full_unstemmed DHA but not EPA induces the trans-differentiation of C2C12 cells into white-like adipocytes phenotype.
title_sort dha but not epa induces the trans-differentiation of c2c12 cells into white-like adipocytes phenotype.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/f1c5ee6965fd4c52a17c0cac329f1279
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AT jamiebaum dhabutnotepainducesthetransdifferentiationofc2c12cellsintowhitelikeadipocytesphenotype
AT yanhuang dhabutnotepainducesthetransdifferentiationofc2c12cellsintowhitelikeadipocytesphenotype
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