Ochratoxin A Induces Steatosis via PPARγ-CD36 Axis

Ochratoxin A(OTA) is considered to be one of the most important contaminants of food and feed worldwide. The liver is one of key target organs for OTA to exert its toxic effects. Due to current lifestyle and diet, nonalcoholic fatty liver disease (NAFLD) has been the most common liver disease. To ex...

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Autores principales: Qian-Wen Zheng, Xu-Fen Ding, Hui-Jun Cao, Qian-Zhi Ni, Bing Zhu, Ning Ma, Feng-Kun Zhang, Yi-Kang Wang, Sheng Xu, Tian-Wei Chen, Ji Xia, Xiao-Song Qiu, Dian-Zhen Yu, Dong Xie, Jing-Jing Li
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Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/b74733d14f964bbc8a2d6186af0a8b0f
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spelling oai:doaj.org-article:b74733d14f964bbc8a2d6186af0a8b0f2021-11-25T19:08:57ZOchratoxin A Induces Steatosis via PPARγ-CD36 Axis10.3390/toxins131108022072-6651https://doaj.org/article/b74733d14f964bbc8a2d6186af0a8b0f2021-11-01T00:00:00Zhttps://www.mdpi.com/2072-6651/13/11/802https://doaj.org/toc/2072-6651Ochratoxin A(OTA) is considered to be one of the most important contaminants of food and feed worldwide. The liver is one of key target organs for OTA to exert its toxic effects. Due to current lifestyle and diet, nonalcoholic fatty liver disease (NAFLD) has been the most common liver disease. To examine the potential effect of OTA on hepatic lipid metabolism and NAFLD, C57BL/6 male mice received 1 mg/kg OTA by gavage daily. Compared with controls, OTA increased lipid deposition and TG accumulation in mouse livers. In vitro OTA treatment also promoted lipid droplets accumulation in primary hepatocytes and HepG2 cells. Mechanistically, OTA prevented PPARγ degradation by reducing the interaction between PPARγ and its E3 ligase SIAH2, which led to activation of PPARγ signaling pathway. Furthermore, downregulation or inhibition of CD36, a known of PPARγ, alleviated OTA-induced lipid droplets deposition and TG accumulation. Therefore, OTA induces hepatic steatosis via PPARγ-CD36 axis, suggesting that OTA has an impact on liver lipid metabolism and may contribute to the development of metabolic diseases.Qian-Wen ZhengXu-Fen DingHui-Jun CaoQian-Zhi NiBing ZhuNing MaFeng-Kun ZhangYi-Kang WangSheng XuTian-Wei ChenJi XiaXiao-Song QiuDian-Zhen YuDong XieJing-Jing LiMDPI AGarticlefatty liver diseaselipid metabolismOTAPPARMedicineRENToxins, Vol 13, Iss 802, p 802 (2021)
institution DOAJ
collection DOAJ
language EN
topic fatty liver disease
lipid metabolism
OTA
PPAR
Medicine
R
spellingShingle fatty liver disease
lipid metabolism
OTA
PPAR
Medicine
R
Qian-Wen Zheng
Xu-Fen Ding
Hui-Jun Cao
Qian-Zhi Ni
Bing Zhu
Ning Ma
Feng-Kun Zhang
Yi-Kang Wang
Sheng Xu
Tian-Wei Chen
Ji Xia
Xiao-Song Qiu
Dian-Zhen Yu
Dong Xie
Jing-Jing Li
Ochratoxin A Induces Steatosis via PPARγ-CD36 Axis
description Ochratoxin A(OTA) is considered to be one of the most important contaminants of food and feed worldwide. The liver is one of key target organs for OTA to exert its toxic effects. Due to current lifestyle and diet, nonalcoholic fatty liver disease (NAFLD) has been the most common liver disease. To examine the potential effect of OTA on hepatic lipid metabolism and NAFLD, C57BL/6 male mice received 1 mg/kg OTA by gavage daily. Compared with controls, OTA increased lipid deposition and TG accumulation in mouse livers. In vitro OTA treatment also promoted lipid droplets accumulation in primary hepatocytes and HepG2 cells. Mechanistically, OTA prevented PPARγ degradation by reducing the interaction between PPARγ and its E3 ligase SIAH2, which led to activation of PPARγ signaling pathway. Furthermore, downregulation or inhibition of CD36, a known of PPARγ, alleviated OTA-induced lipid droplets deposition and TG accumulation. Therefore, OTA induces hepatic steatosis via PPARγ-CD36 axis, suggesting that OTA has an impact on liver lipid metabolism and may contribute to the development of metabolic diseases.
format article
author Qian-Wen Zheng
Xu-Fen Ding
Hui-Jun Cao
Qian-Zhi Ni
Bing Zhu
Ning Ma
Feng-Kun Zhang
Yi-Kang Wang
Sheng Xu
Tian-Wei Chen
Ji Xia
Xiao-Song Qiu
Dian-Zhen Yu
Dong Xie
Jing-Jing Li
author_facet Qian-Wen Zheng
Xu-Fen Ding
Hui-Jun Cao
Qian-Zhi Ni
Bing Zhu
Ning Ma
Feng-Kun Zhang
Yi-Kang Wang
Sheng Xu
Tian-Wei Chen
Ji Xia
Xiao-Song Qiu
Dian-Zhen Yu
Dong Xie
Jing-Jing Li
author_sort Qian-Wen Zheng
title Ochratoxin A Induces Steatosis via PPARγ-CD36 Axis
title_short Ochratoxin A Induces Steatosis via PPARγ-CD36 Axis
title_full Ochratoxin A Induces Steatosis via PPARγ-CD36 Axis
title_fullStr Ochratoxin A Induces Steatosis via PPARγ-CD36 Axis
title_full_unstemmed Ochratoxin A Induces Steatosis via PPARγ-CD36 Axis
title_sort ochratoxin a induces steatosis via pparγ-cd36 axis
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/b74733d14f964bbc8a2d6186af0a8b0f
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