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Title: HMGB1 induces an inflammatory response in endothelial cells via the RAGE-dependent endoplasmic reticulum stress pathway

Abstract

Highlights: •Mechanisms of inflammatory response induced by HMGB1 are incompletely understood. •We found that endoplasmic reticulum stress mediate the inflammatory response induced by HMGB1. •RAGE-mediated ERS pathways are involved in those processes. •We reported a new mechanism for HMGB1 induced inflammatory response. -- Abstract: The high mobility group 1B protein (HMGB1) mediates chronic inflammatory responses in endothelial cells, which play a critical role in atherosclerosis. However, the underlying mechanism is unknown. The goal of our study was to identify the effects of HMGB1 on the RAGE-induced inflammatory response in endothelial cells and test the possible involvement of the endoplasmic reticulum stress pathway. Our results showed that incubation of endothelial cells with HMGB1 (0.01–1 μg/ml) for 24 h induced a dose-dependent activation of endoplasmic reticulum stress transducers, as assessed by PERK and IRE1 protein expression. Moreover, HMGB1 also promoted nuclear translocation of ATF6. HMGB1-mediated ICAM-1 and P-selectin production was dramatically suppressed by PERK siRNA or IRE1 siRNA. However, non-targeting siRNA had no such effects. HMGB1-induced increases in ICAM-1 and P-selectin expression were also inhibited by a specific eIF2α inhibitor (salubrinal) and a specific JNK inhibitor (SP600125). Importantly, a blocking antibody specifically targeted against RAGE (anti-RAGE antibody) decreased ICAM-1, P-selectin and endoplasmicmore » reticulum stress molecule (PERK, eIF2α, IRE1 and JNK) protein expression levels. Collectively, these novel findings suggest that HMGB1 promotes an inflammatory response by inducing the expression of ICAM-1 and P-selectin via RAGE-mediated stimulation of the endoplasmic reticulum stress pathway.« less

Authors:
 [1];  [2];  [1];  [3];  [4]
  1. Department of Geriatric Medicine, Xiangya Hospital, Central South University, Changsha 410078 (China)
  2. Department of Cardiovascular Medicine, Xiangya Hospital, Central South University, Changsha 410078 (China)
  3. Department of Otolaryngology, Xiangya Hospital, Central South University, Changsha 410078 (China)
  4. Department of Hematology, Xiangya Hospital, Central South University, Changsha 410078 (China)
Publication Date:
OSTI Identifier:
22242086
Resource Type:
Journal Article
Resource Relation:
Journal Name: Biochemical and Biophysical Research Communications; Journal Volume: 438; Journal Issue: 4; Other Information: Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Country of Publication:
United States
Language:
English
Subject:
60 APPLIED LIFE SCIENCES; ANTIBODIES; ARTERIOSCLEROSIS; ENDOPLASMIC RETICULUM; INFLAMMATION; PROTEINS

Citation Formats

Luo, Ying, Li, Shu-Jun, Yang, Jian, Qiu, Yuan-Zhen, and Chen, Fang-Ping, E-mail: xychenfp@163.com. HMGB1 induces an inflammatory response in endothelial cells via the RAGE-dependent endoplasmic reticulum stress pathway. United States: N. p., 2013. Web. doi:10.1016/J.BBRC.2013.07.098.
Luo, Ying, Li, Shu-Jun, Yang, Jian, Qiu, Yuan-Zhen, & Chen, Fang-Ping, E-mail: xychenfp@163.com. HMGB1 induces an inflammatory response in endothelial cells via the RAGE-dependent endoplasmic reticulum stress pathway. United States. doi:10.1016/J.BBRC.2013.07.098.
Luo, Ying, Li, Shu-Jun, Yang, Jian, Qiu, Yuan-Zhen, and Chen, Fang-Ping, E-mail: xychenfp@163.com. Fri . "HMGB1 induces an inflammatory response in endothelial cells via the RAGE-dependent endoplasmic reticulum stress pathway". United States. doi:10.1016/J.BBRC.2013.07.098.
@article{osti_22242086,
title = {HMGB1 induces an inflammatory response in endothelial cells via the RAGE-dependent endoplasmic reticulum stress pathway},
author = {Luo, Ying and Li, Shu-Jun and Yang, Jian and Qiu, Yuan-Zhen and Chen, Fang-Ping, E-mail: xychenfp@163.com},
abstractNote = {Highlights: •Mechanisms of inflammatory response induced by HMGB1 are incompletely understood. •We found that endoplasmic reticulum stress mediate the inflammatory response induced by HMGB1. •RAGE-mediated ERS pathways are involved in those processes. •We reported a new mechanism for HMGB1 induced inflammatory response. -- Abstract: The high mobility group 1B protein (HMGB1) mediates chronic inflammatory responses in endothelial cells, which play a critical role in atherosclerosis. However, the underlying mechanism is unknown. The goal of our study was to identify the effects of HMGB1 on the RAGE-induced inflammatory response in endothelial cells and test the possible involvement of the endoplasmic reticulum stress pathway. Our results showed that incubation of endothelial cells with HMGB1 (0.01–1 μg/ml) for 24 h induced a dose-dependent activation of endoplasmic reticulum stress transducers, as assessed by PERK and IRE1 protein expression. Moreover, HMGB1 also promoted nuclear translocation of ATF6. HMGB1-mediated ICAM-1 and P-selectin production was dramatically suppressed by PERK siRNA or IRE1 siRNA. However, non-targeting siRNA had no such effects. HMGB1-induced increases in ICAM-1 and P-selectin expression were also inhibited by a specific eIF2α inhibitor (salubrinal) and a specific JNK inhibitor (SP600125). Importantly, a blocking antibody specifically targeted against RAGE (anti-RAGE antibody) decreased ICAM-1, P-selectin and endoplasmic reticulum stress molecule (PERK, eIF2α, IRE1 and JNK) protein expression levels. Collectively, these novel findings suggest that HMGB1 promotes an inflammatory response by inducing the expression of ICAM-1 and P-selectin via RAGE-mediated stimulation of the endoplasmic reticulum stress pathway.},
doi = {10.1016/J.BBRC.2013.07.098},
journal = {Biochemical and Biophysical Research Communications},
number = 4,
volume = 438,
place = {United States},
year = {Fri Sep 06 00:00:00 EDT 2013},
month = {Fri Sep 06 00:00:00 EDT 2013}
}
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