Published August 1, 2017 | Version v1
Journal article

HMGA2, a driver of inflammation, is associated with hypermethylation in acute liver injury

  • 1. Institute for Liver Diseases of Anhui Medical University (China)
  • 2. The Key Laboratory of Anti-inflammatory of Immune Medicines, Ministry of Education (China)
  • 3. The Key Laboratory of Major Autoimmune Diseases, Anhui Province, Anhui Institute of Innovative Drugs, School of Pharmacy, Anhui Medical University (China)

Description

Acute liver injury (ALI) is characteristic of abrupt hepatic dysfunction and inflammatory response. Activaion of Kupffer cells (KCs) plays a central role in the pathogenesis of ALI. Since the High Mobility Group A protein2 (HMGA2) occurs as a driver at critical stage of hepatocellular carcinoma, herein, we investigated the role of HMGA2 in macrophage activation during ALI. Our study found that the expression of HMGA2 decreased dramatically both in KCs isolated from the liver in mice with ALI and in LPS-induced RAW264.7 cell lines. Moreover, loss- and gain-of-function studies suggested that HMGA2 could enhance the expression of pro-inflammatory cytokines including TNF-α, IL-6 and IL-1β. These results indicated that HMGA2 may play an essential role in macrophage activation during ALI. Additionally, our results showed the expression of HMGA2 was up-regulated when LPS-induced RAW264.7 cells were treated with 5-aza-2-deoxycytidine. Furthermore, silencing of DNMT1, DNMT3a, DNMT3b could respectively prevent the down-expression of HMGA2 in LPS-induced RAW264.7 cells. In conclusion, HMGA2 promotes the release of pro-inflammatory cytokines through NF-κB pathway, and the dysregulation of HMGA2 may involve with hypermethylation. - Highlights: • HMGA2 was screened through RRBS by our research group. • Our study provides the first evidence to demonstrated the function of HMGA2 in acute liver injury. • HMGA2 mediated inflammation is associated with hypermethylation was illustrated for the first time.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.taap.2017.05.005

Additional details

Identifiers

DOI
10.1016/j.taap.2017.05.005;
PII
S0041-008X(17)30199-0;

Publishing Information

Journal Title
Toxicology and Applied Pharmacology
Journal Volume
328
Journal Page Range
p. 34-45
ISSN
0041-008X
CODEN
TXAPA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
49073690
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
ANNUAL LIMIT OF INTAKE; INFLAMMATION; INJURIES; LIVER; RETICULOENDOTHELIAL SYSTEM
Descriptors DEC
ANIMAL TISSUES; BODY; DIGESTIVE SYSTEM; DISEASES; GLANDS; ORGANS; PATHOLOGICAL CHANGES; SAFETY STANDARDS; STANDARDS; SYMPTOMS

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.