TY - JOUR
T1 - Location is the key to function
T2 - HMGB1 in sepsis and trauma-induced inflammation
AU - Deng, Meihong
AU - Scott, Melanie J.
AU - Fan, Jie
AU - Billiar, Timothy R.
N1 - Publisher Copyright:
©2019 Society for Leukocyte Biology
PY - 2019/7
Y1 - 2019/7
N2 - High mobility group box 1 (HMGB1) is a multifunctional nuclear protein, probably known best as a prototypical alarmin or damage-associated molecular pattern (DAMP) molecule when released from cells. However, HMGB1 has multiple functions that depend on its location in the nucleus, in the cytosol, or extracellularly after either active release from cells, or passive release upon lytic cell death. Movement of HMGB1 between cellular compartments is a dynamic process induced by a variety of cell stresses and disease processes, including sepsis, trauma, and hemorrhagic shock. Location of HMGB1 is intricately linked with its function and is regulated by a series of posttranslational modifications. HMGB1 function is also regulated by the redox status of critical cysteine residues within the protein, and is cell-type dependent. This review highlights some of the mechanisms that contribute to location and functions of HMGB1, and focuses on some recent insights on important intracellular effects of HMGB1 during sepsis and trauma.
AB - High mobility group box 1 (HMGB1) is a multifunctional nuclear protein, probably known best as a prototypical alarmin or damage-associated molecular pattern (DAMP) molecule when released from cells. However, HMGB1 has multiple functions that depend on its location in the nucleus, in the cytosol, or extracellularly after either active release from cells, or passive release upon lytic cell death. Movement of HMGB1 between cellular compartments is a dynamic process induced by a variety of cell stresses and disease processes, including sepsis, trauma, and hemorrhagic shock. Location of HMGB1 is intricately linked with its function and is regulated by a series of posttranslational modifications. HMGB1 function is also regulated by the redox status of critical cysteine residues within the protein, and is cell-type dependent. This review highlights some of the mechanisms that contribute to location and functions of HMGB1, and focuses on some recent insights on important intracellular effects of HMGB1 during sepsis and trauma.
KW - AIM2
KW - DAMPs
KW - autophagy
KW - caspase-11
KW - pyroptosis
UR - http://www.scopus.com/inward/record.url?scp=85063963560&partnerID=8YFLogxK
U2 - 10.1002/JLB.3MIR1218-497R
DO - 10.1002/JLB.3MIR1218-497R
M3 - Review article
C2 - 30946496
AN - SCOPUS:85063963560
SN - 0741-5400
VL - 106
SP - 161
EP - 169
JO - Journal of Leukocyte Biology
JF - Journal of Leukocyte Biology
IS - 1
ER -