The Role of Autophagy and NLRP3 Inflammasome in Liver Fibrosis
Liver fibrosis is an intrinsic repair process of chronic injury with excessive deposition of extracellular matrix. As an early stage of various liver diseases, liver fibrosis is a reversible pathological process. Therefore, if not being controlled in time, liver fibrosis will evolve into cirrhosis,...
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2020-01-01
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Series: | BioMed Research International |
Online Access: | http://dx.doi.org/10.1155/2020/7269150 |
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doaj-39e5f021657646e794f09a802c32cc292020-11-25T03:34:55ZengHindawi LimitedBioMed Research International2314-61332314-61412020-01-01202010.1155/2020/72691507269150The Role of Autophagy and NLRP3 Inflammasome in Liver FibrosisYe Tao0Ningning Wang1Tianming Qiu2Xiance Sun3Occupational and Environmental Health Department, Dalian Medical University, 9 Lvshun South Road, Dalian 116044, ChinaNutrition and Food Hygiene, Dalian Medical University, 9 Lvshun South Road, Dalian 116044, ChinaOccupational and Environmental Health Department, Dalian Medical University, 9 Lvshun South Road, Dalian 116044, ChinaOccupational and Environmental Health Department, Dalian Medical University, 9 Lvshun South Road, Dalian 116044, ChinaLiver fibrosis is an intrinsic repair process of chronic injury with excessive deposition of extracellular matrix. As an early stage of various liver diseases, liver fibrosis is a reversible pathological process. Therefore, if not being controlled in time, liver fibrosis will evolve into cirrhosis, liver failure, and liver cancer. It has been demonstrated that hepatic stellate cells (HSCs) play a crucial role in the formation of liver fibrosis. In particular, the activation of HSCs is a key step for liver fibrosis. Recent researches have suggested that autophagy and inflammasome have biological effect on HSC activation. Herein, we review current studies about the impact of autophagy and NOD-like receptors containing pyrin domain 3 (NLRP3) inflammasome on liver fibrosis and the underlying mechanisms.http://dx.doi.org/10.1155/2020/7269150 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ye Tao Ningning Wang Tianming Qiu Xiance Sun |
spellingShingle |
Ye Tao Ningning Wang Tianming Qiu Xiance Sun The Role of Autophagy and NLRP3 Inflammasome in Liver Fibrosis BioMed Research International |
author_facet |
Ye Tao Ningning Wang Tianming Qiu Xiance Sun |
author_sort |
Ye Tao |
title |
The Role of Autophagy and NLRP3 Inflammasome in Liver Fibrosis |
title_short |
The Role of Autophagy and NLRP3 Inflammasome in Liver Fibrosis |
title_full |
The Role of Autophagy and NLRP3 Inflammasome in Liver Fibrosis |
title_fullStr |
The Role of Autophagy and NLRP3 Inflammasome in Liver Fibrosis |
title_full_unstemmed |
The Role of Autophagy and NLRP3 Inflammasome in Liver Fibrosis |
title_sort |
role of autophagy and nlrp3 inflammasome in liver fibrosis |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2020-01-01 |
description |
Liver fibrosis is an intrinsic repair process of chronic injury with excessive deposition of extracellular matrix. As an early stage of various liver diseases, liver fibrosis is a reversible pathological process. Therefore, if not being controlled in time, liver fibrosis will evolve into cirrhosis, liver failure, and liver cancer. It has been demonstrated that hepatic stellate cells (HSCs) play a crucial role in the formation of liver fibrosis. In particular, the activation of HSCs is a key step for liver fibrosis. Recent researches have suggested that autophagy and inflammasome have biological effect on HSC activation. Herein, we review current studies about the impact of autophagy and NOD-like receptors containing pyrin domain 3 (NLRP3) inflammasome on liver fibrosis and the underlying mechanisms. |
url |
http://dx.doi.org/10.1155/2020/7269150 |
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