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Free fatty acid-induced histone acetyltransferase activity accelerates lipid accumulation in HepG2 cells
BACKGROUND/OBJECTIVES: Non-alcoholic fatty liver disease (NAFLD) is a common metabolic disease triggered by epigenetic alterations, including lysine acetylation at histone or non-histone proteins, affecting the stability or transcription of lipogenic genes. Although various natural dietary compounds...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Nutrition Society and the Korean Society of Community Nutrition
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6548710/ https://www.ncbi.nlm.nih.gov/pubmed/31214287 http://dx.doi.org/10.4162/nrp.2019.13.3.196 |
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author | Chung, Sangwon Hwang, Jin-Taek Park, Jae Ho Choi, Hyo-Kyoung |
author_facet | Chung, Sangwon Hwang, Jin-Taek Park, Jae Ho Choi, Hyo-Kyoung |
author_sort | Chung, Sangwon |
collection | PubMed |
description | BACKGROUND/OBJECTIVES: Non-alcoholic fatty liver disease (NAFLD) is a common metabolic disease triggered by epigenetic alterations, including lysine acetylation at histone or non-histone proteins, affecting the stability or transcription of lipogenic genes. Although various natural dietary compounds have anti-lipogenic effects, their effects on the acetylation status and lipid metabolism in the liver have not been thoroughly investigated. MATERIALS/METHODS: Following oleic-palmitic acid (OPA)-induced lipid accumulation in HepG2 cells, the acetylation status of histone and non-histone proteins, HAT activity, and mRNA expression of representative lipogenic genes, including PPARγ, SREBP-1c, ACLY, and FASN, were evaluated. Furthermore, correlations between lipid accumulation and HAT activity for 22 representative natural food extracts (NExs) were evaluated. RESULTS: Non-histone protein acetylation increased following OPA treatment and the acetylation of histones H3K9, H4K8, and H4K16 was accelerated, accompanied by an increase in HAT activity. OPA-induced increases in the mRNA expression of lipogenic genes were down-regulated by C-646, a p300/CBP-specific inhibitor. Finally, we detected a positive correlation between HAT activity and lipid accumulation (Pearson's correlation coefficient = 0.604) using 22 NExs. CONCLUSIONS: Our results suggest that NExs have novel applications as nutraceutical agents with HAT inhibitor activity for the prevention and treatment of NAFLD. |
format | Online Article Text |
id | pubmed-6548710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Korean Nutrition Society and the Korean Society of Community Nutrition |
record_format | MEDLINE/PubMed |
spelling | pubmed-65487102019-06-18 Free fatty acid-induced histone acetyltransferase activity accelerates lipid accumulation in HepG2 cells Chung, Sangwon Hwang, Jin-Taek Park, Jae Ho Choi, Hyo-Kyoung Nutr Res Pract Original Research BACKGROUND/OBJECTIVES: Non-alcoholic fatty liver disease (NAFLD) is a common metabolic disease triggered by epigenetic alterations, including lysine acetylation at histone or non-histone proteins, affecting the stability or transcription of lipogenic genes. Although various natural dietary compounds have anti-lipogenic effects, their effects on the acetylation status and lipid metabolism in the liver have not been thoroughly investigated. MATERIALS/METHODS: Following oleic-palmitic acid (OPA)-induced lipid accumulation in HepG2 cells, the acetylation status of histone and non-histone proteins, HAT activity, and mRNA expression of representative lipogenic genes, including PPARγ, SREBP-1c, ACLY, and FASN, were evaluated. Furthermore, correlations between lipid accumulation and HAT activity for 22 representative natural food extracts (NExs) were evaluated. RESULTS: Non-histone protein acetylation increased following OPA treatment and the acetylation of histones H3K9, H4K8, and H4K16 was accelerated, accompanied by an increase in HAT activity. OPA-induced increases in the mRNA expression of lipogenic genes were down-regulated by C-646, a p300/CBP-specific inhibitor. Finally, we detected a positive correlation between HAT activity and lipid accumulation (Pearson's correlation coefficient = 0.604) using 22 NExs. CONCLUSIONS: Our results suggest that NExs have novel applications as nutraceutical agents with HAT inhibitor activity for the prevention and treatment of NAFLD. The Korean Nutrition Society and the Korean Society of Community Nutrition 2019-06 2019-04-12 /pmc/articles/PMC6548710/ /pubmed/31214287 http://dx.doi.org/10.4162/nrp.2019.13.3.196 Text en ©2019 The Korean Nutrition Society and the Korean Society of Community Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Chung, Sangwon Hwang, Jin-Taek Park, Jae Ho Choi, Hyo-Kyoung Free fatty acid-induced histone acetyltransferase activity accelerates lipid accumulation in HepG2 cells |
title | Free fatty acid-induced histone acetyltransferase activity accelerates lipid accumulation in HepG2 cells |
title_full | Free fatty acid-induced histone acetyltransferase activity accelerates lipid accumulation in HepG2 cells |
title_fullStr | Free fatty acid-induced histone acetyltransferase activity accelerates lipid accumulation in HepG2 cells |
title_full_unstemmed | Free fatty acid-induced histone acetyltransferase activity accelerates lipid accumulation in HepG2 cells |
title_short | Free fatty acid-induced histone acetyltransferase activity accelerates lipid accumulation in HepG2 cells |
title_sort | free fatty acid-induced histone acetyltransferase activity accelerates lipid accumulation in hepg2 cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6548710/ https://www.ncbi.nlm.nih.gov/pubmed/31214287 http://dx.doi.org/10.4162/nrp.2019.13.3.196 |
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