Extracellular RNA mediates iron-induced toxicity and inflammatory signalling in hepatic cells

Hepatic iron accumulation and toxicity is a frequent finding in chronic liver diseases such as hereditary hemochromatosis (HH), metabolic associated fatty liver disease (MASLD), alcoholic liver disease (ALD) and hepatitis C virus (HCV) infection, however, it's contribution to disease pathology is not fully understood. Here, using HepG2 cells we show that iron induced hepatocyte damage triggers the release of extracellular RNAs (eRNAs), which bind to the toll-like receptor 3 (TLR3), resulting in the production of pro-inflammatory cytokines. Furthermore, the inhibition of eRNA activity by RNase1 and TLR3 inhibitor significantly improved cell viability as well as NLRP3 and NF-kB-mediated inflammatory signalling. Therefore, eRNA antagonism could represent a novel therapeutic approach to reduce iron-induced inflammation in chronic liver diseases.

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Publication Details

Journal
Toxicology Reports
Published
2025-03-18
DOI
https://doi.org/10.1016/j.toxrep.2025.102002
Citations
3
Primary Topic
RNA regulation and disease
Type
article
Field-Weighted Citation Impact
2.42
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article

Extracellular RNA mediates iron-induced toxicity and inflammatory signalling in hepatic cells

Sangam Rajak, Pratima Gupta, Sana Raza, Rohit A. Sinha et al.
3 citations
Toxicology Reports
RNA regulation and disease
2.42
article

Extracellular RNA mediates iron-induced toxicity and inflammatory signalling in hepatic cells

Sangam Rajak, Pratima Gupta, Sana Raza, Rohit A. Sinha, Archana Tewari
article en
3 citations

Abstract

Hepatic iron accumulation and toxicity is a frequent finding in chronic liver diseases such as hereditary hemochromatosis (HH), metabolic associated fatty liver disease (MASLD), alcoholic liver disease (ALD) and hepatitis C virus (HCV) infection, however, it's contribution to disease pathology is not fully understood. Here, using HepG2 cells we show that iron induced hepatocyte damage triggers the release of extracellular RNAs (eRNAs), which bind to the toll-like receptor 3 (TLR3), resulting in the production of pro-inflammatory cytokines. Furthermore, the inhibition of eRNA activity by RNase1 and TLR3 inhibitor significantly improved cell viability as well as NLRP3 and NF-kB-mediated inflammatory signalling. Therefore, eRNA antagonism could represent a novel therapeutic approach to reduce iron-induced inflammation in chronic liver diseases.

Toxicology ReportsVol. 14
Sanjay Gandhi Post Graduate Institute of Medical Sciences (IN)
Zero hunger
Openalex Percentile: Top 13%
RNA regulation and disease
2.42
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