Cargando…

In vitro inhibition of hepatic stellate cell activation by the autophagy-related lipid droplet protein ATG2A

Clinical studies have found that moderate intake of retinol or oleic acid can enlarge the lipid droplets of hepatic stellate cells and suppress their activation. However, the link between lipid droplets and cell activation is unknown. This study compared the dynamics of lipid droplet-associated prot...

Descripción completa

Detalles Bibliográficos
Autores principales: Hong, Yun, Li, Sirui, Wang, Jifeng, Li, Youming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006255/
https://www.ncbi.nlm.nih.gov/pubmed/29915313
http://dx.doi.org/10.1038/s41598-018-27686-6
_version_ 1783332803524427776
author Hong, Yun
Li, Sirui
Wang, Jifeng
Li, Youming
author_facet Hong, Yun
Li, Sirui
Wang, Jifeng
Li, Youming
author_sort Hong, Yun
collection PubMed
description Clinical studies have found that moderate intake of retinol or oleic acid can enlarge the lipid droplets of hepatic stellate cells and suppress their activation. However, the link between lipid droplets and cell activation is unknown. This study compared the dynamics of lipid droplet-associated protein expression between activated and reverted stellate cells. Reversion of the activated human stellate cell line LX-2 and inhibition of primary mouse stellate cell activation were induced by retinol or oleic acid, which resulted in larger lipid droplets and the downregulation of cell activation markers. Quantitative proteomics and immunoblotting were performed to compare lipid-droplet protein profiles between activated and reverted LX-2 cells. Compared to expression in activated cells, 50 lipid-droplet proteins were upregulated, whereas 28 were downregulated upon reversion. ATG2A was significantly enriched in lipid droplets of retinol/oleic acid-treated LX-2 cells and quiescent primary stellate cells. Reduced expression of α-SMA, increased expression of perilipin-3, enlarged lipid droplets, and suppression of autophagic flux were observed in ATG2A-deficient LX2 cells. Lipid-droplet protein profile changes during the reversion of activated stellate cells might provide new insights into the molecular mechanisms linking lipid droplets to liver fibrosis. ATG2A could represent a potential new drug target for hepatic fibrosis.
format Online
Article
Text
id pubmed-6006255
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-60062552018-06-26 In vitro inhibition of hepatic stellate cell activation by the autophagy-related lipid droplet protein ATG2A Hong, Yun Li, Sirui Wang, Jifeng Li, Youming Sci Rep Article Clinical studies have found that moderate intake of retinol or oleic acid can enlarge the lipid droplets of hepatic stellate cells and suppress their activation. However, the link between lipid droplets and cell activation is unknown. This study compared the dynamics of lipid droplet-associated protein expression between activated and reverted stellate cells. Reversion of the activated human stellate cell line LX-2 and inhibition of primary mouse stellate cell activation were induced by retinol or oleic acid, which resulted in larger lipid droplets and the downregulation of cell activation markers. Quantitative proteomics and immunoblotting were performed to compare lipid-droplet protein profiles between activated and reverted LX-2 cells. Compared to expression in activated cells, 50 lipid-droplet proteins were upregulated, whereas 28 were downregulated upon reversion. ATG2A was significantly enriched in lipid droplets of retinol/oleic acid-treated LX-2 cells and quiescent primary stellate cells. Reduced expression of α-SMA, increased expression of perilipin-3, enlarged lipid droplets, and suppression of autophagic flux were observed in ATG2A-deficient LX2 cells. Lipid-droplet protein profile changes during the reversion of activated stellate cells might provide new insights into the molecular mechanisms linking lipid droplets to liver fibrosis. ATG2A could represent a potential new drug target for hepatic fibrosis. Nature Publishing Group UK 2018-06-18 /pmc/articles/PMC6006255/ /pubmed/29915313 http://dx.doi.org/10.1038/s41598-018-27686-6 Text en © The Author(s) 2018 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/.
spellingShingle Article
Hong, Yun
Li, Sirui
Wang, Jifeng
Li, Youming
In vitro inhibition of hepatic stellate cell activation by the autophagy-related lipid droplet protein ATG2A
title In vitro inhibition of hepatic stellate cell activation by the autophagy-related lipid droplet protein ATG2A
title_full In vitro inhibition of hepatic stellate cell activation by the autophagy-related lipid droplet protein ATG2A
title_fullStr In vitro inhibition of hepatic stellate cell activation by the autophagy-related lipid droplet protein ATG2A
title_full_unstemmed In vitro inhibition of hepatic stellate cell activation by the autophagy-related lipid droplet protein ATG2A
title_short In vitro inhibition of hepatic stellate cell activation by the autophagy-related lipid droplet protein ATG2A
title_sort in vitro inhibition of hepatic stellate cell activation by the autophagy-related lipid droplet protein atg2a
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006255/
https://www.ncbi.nlm.nih.gov/pubmed/29915313
http://dx.doi.org/10.1038/s41598-018-27686-6
work_keys_str_mv AT hongyun invitroinhibitionofhepaticstellatecellactivationbytheautophagyrelatedlipiddropletproteinatg2a
AT lisirui invitroinhibitionofhepaticstellatecellactivationbytheautophagyrelatedlipiddropletproteinatg2a
AT wangjifeng invitroinhibitionofhepaticstellatecellactivationbytheautophagyrelatedlipiddropletproteinatg2a
AT liyouming invitroinhibitionofhepaticstellatecellactivationbytheautophagyrelatedlipiddropletproteinatg2a