The multifunctional protein HMGB1: 50 years of discovery

D Tang, R Kang, HJ Zeh, MT Lotze - Nature Reviews Immunology, 2023 - nature.com
Fifty years since the initial discovery of HMGB1 in 1973 as a structural protein of chromatin,
HMGB1 is now known to regulate diverse biological processes depending on its subcellular …

Targeting inflammation driven by HMGB1

H Yang, H Wang, U Andersson - Frontiers in immunology, 2020 - frontiersin.org
High mobility group box 1 (HMGB1) is a highly conserved, nuclear protein present in all cell
types. It is a multi-facet protein exerting functions both inside and outside of cells …

RAGE and TLRs: relatives, friends or neighbours?

ZA Ibrahim, CL Armour, S Phipps, MB Sukkar - Molecular immunology, 2013 - Elsevier
The innate immune system forms the first line of protection against infectious and non-
infectious tissue injury. Cells of the innate immune system detect pathogen-associated …

Glycyrrhizin inhibits traumatic brain injury by reducing HMGB1–RAGE interaction

YU Okuma, K Liu, H Wake, R Liu, Y Nishimura, Z Hui… - …, 2014 - Elsevier
Glycyrrhizin (GL) is a major constituent of licorice root and has been suggested to inhibit the
release of high mobility group box-1 (HMGB1), a protein considered representative of …

HMGB1: a double-edged sword and therapeutic target in the female reproductive system

Y Ren, D Zhu, X Han, Q Zhang, B Chen… - Frontiers in …, 2023 - frontiersin.org
HMGB1 that belongs to the High Mobility Group-box superfamily, is a nonhistone chromatin
associated transcription factor. It is present in the nucleus of eukaryotes and can be actively …

Endogenous regulation and pharmacological modulation of sepsis-induced HMGB1 release and action: An updated review

CS Zhu, W Wang, X Qiang, W Chen, X Lan, J Li… - Cells, 2021 - mdpi.com
Sepsis remains a common cause of death in intensive care units, accounting for
approximately 20% of total deaths worldwide. Its pathogenesis is partly attributable to …

[PDF][PDF] The importance of Ca2+/Zn2+ signaling S100 proteins and RAGE in translational medicine

E Leclerc, CW Heizmann - Front Biosci (Schol Ed), 2011 - article.imrpress.com
Introduction 3. General features of S100 proteins 4. The receptor for advanced glycation
endproducts (RAGE) 5. Structures and functions of S100 proteins and RAGE: association …

Macrophage-derived HMGB1 as a pain mediator in the early stage of acute pancreatitis in mice: targeting RAGE and CXCL12/CXCR4 axis

Y Irie, M Tsubota, H Ishikura, F Sekiguchi… - Journal of Neuroimmune …, 2017 - Springer
Extracellular high mobility group box 1 (HMGB1) activates the receptor for advanced
glycation end products (RAGE) or Toll-like receptor 4 (TLR4) and forms a heterocomplex …

Involvement of high mobility group box 1 in the development and maintenance of chemotherapy-induced peripheral neuropathy in rats

T Nishida, M Tsubota, Y Kawaishi, H Yamanishi… - Toxicology, 2016 - Elsevier
Given that high mobility group box 1 (HMGB1), a nuclear protein, once released to the
extracellular space, promotes nociception, we asked if inactivation of HMGB1 prevents or …

The IKKα-dependent NF-κB p52/RelB noncanonical pathway is essential to sustain a CXCL12 autocrine loop in cells migrating in response to HMGB1

RR Kew, M Penzo, DM Habiel… - The Journal of …, 2012 - journals.aai.org
HMGB1 is a chromatin architectural protein that is released by dead or damaged cells at
sites of tissue injury. Extracellular HMGB1 functions as a proinflammatory cytokine and …