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Cited by 332

The DOI matches its Crossref record; 97 of the 97 references it cites were found in a registry or an index.

The role of extracellular histone in organ injury

Open access
Silk, Eleanor, Zhao, Hailin, Weng, Hao, Ma, Daqing·2017·Cell Death & Disease

Abstract

Histones are intra-nuclear cationic proteins that are present in all eukaryotic cells and are highly conserved across species. Within the nucleus, they provide structural stability to chromatin and regulate gene expression. Histone may be released into the extracellular space in three forms: freely, as a DNA-bound nucleosome or as part of neutrophil extracellular traps, and all three can be detected in serum after significant cellular death such as sepsis, trauma, ischaemia/reperfusion injury and autoimmune disease. Once in the extracellular space, histones act as damage-associated molecular pattern proteins, activating the immune system and causing further cytotoxicity. They interact with Toll-like receptors (TLRs), complement and the phospholipids of cell membranes inducing endothelial and epithelial cytotoxicity, TLR2/TLR4/TLR9 activation and pro-inflammatory cytokine/chemokine release via MyD88, NFκB and NLRP3 inflammasome-dependent pathways. Drugs that block the release of histone, neutralise circulating histone or block histone signal transduction provide significant protection from mortality in animal models of acute organ injury but warrant further research to inform future clinical applications.

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Metadata

Authors
Silk, E., Zhao, H., Weng, H., & Ma, D.
Venue
Cell Death & Disease
Published
2017-05-25
Volume
8
Issue
5
Pages
e2812-e2812
ISSN
2041-4889 (ISSN-L)
OpenAlex
W2617096708
Cited by
332
References
97
FWCI
9.63
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: The role of extracellular histone in organ injury. https://app.cochat.ai/papers/10.1038/cddis.2017.52
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Silk, E., Zhao, H., Weng, H., & Ma, D. (2017). The role of extracellular histone in organ injury. Cell Death & Disease. https://doi.org/10.1038/cddis.2017.52

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