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  5. The Role of Adipocyte Endoplasmic Reticulum Stress in Obese Adipose Tissue Dysfunction: A Review

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Article
en
2023

The Role of Adipocyte Endoplasmic Reticulum Stress in Obese Adipose Tissue Dysfunction: A Review

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en
2023
Vol Volume 16
Vol. Volume 16
DOI: 10.2147/ijgm.s428482

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Zhong Lin Wang
Zhong Lin Wang

Beijing Institute of Technology

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S. Xu
Jiaqiu Xi
Tao Wu
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Abstract

Abstract: Adipose tissue dysfunction plays an important role in metabolic diseases associated with chronic inflammation, insulin resistance and lipid ectopic deposition in obese patients. In recent years, it has been found that under the stimulation of adipocyte endoplasmic reticulum stress (ERS), the over-activated ER unfolded protein response (UPR) exacerbates the inflammatory response of adipose tissue by interfering with the normal metabolism of adipose tissue, promotes the secretion of adipokines, and affects the browning and thermogenic pathways of adipose tissue, ultimately leading to the manifestation of metabolic syndrome such as ectopic lipid deposition and disorders of glucolipid metabolism in obese patients. This paper mainly summarizes the relationship between adipocyte ERS and obese adipose tissue dysfunction and provides an overview of the mechanisms by which ERS induces metabolic disorders such as catabolism, thermogenesis and inflammation in obese adipose tissue through the regulation of molecules and pathways such as NF-κB, ADPN, STAMP2, LPIN1, TRIP-Br2, NF-Y and SIRT2 and briefly describes the current mechanisms targeting adipocyte endoplasmic reticulum stress to improve obesity and provide ideas for intervention and treatment of obese adipose tissue dysfunction. Keywords: endoplasmic reticulum stress, unfolded protein response, obesity, adipose tissue dysfunction

How to cite this publication

S. Xu, Jiaqiu Xi, Tao Wu, Zhong Lin Wang (2023). The Role of Adipocyte Endoplasmic Reticulum Stress in Obese Adipose Tissue Dysfunction: A Review. , Volume 16, DOI: https://doi.org/10.2147/ijgm.s428482.

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Publication Details

Type

Article

Year

2023

Authors

4

Datasets

0

Total Files

0

Language

en

DOI

https://doi.org/10.2147/ijgm.s428482

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