The translocation of HMGB1 during cell activation and cell death

被引:108
作者
Gauley, Julie [1 ]
Pisetsky, David S. [1 ,2 ]
机构
[1] Duke Univ, Med Ctr, Div Rheumatol & Immunol, Durham, NC USA
[2] Durham VA Hosp, Durham, NC USA
关键词
HMGB1; cytokine; apoptosis; necrosis; POLYINOSINIC-POLYCYTIDYLIC ACID; CHROMATIN PROTEIN HMGB1; GROUP BOX-1 PROTEIN; RELEASE; MACROPHAGES; LIPOPOLYSACCHARIDE; MONOCYTES; HMG-1; MICE;
D O I
10.1080/08916930902831522
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
High-mobility group box protein 1 (HMGB1) is a non-histone nuclear protein with alarmin activity. When present in an extracellular location, HMGB1 can activate the innate immune system and promote inflammation in conditions such as sepsis. To exert these activities, HMGB1 must transit from the nucleus, through the cytoplasm, to the outside of the cell. This process can occur during cell activation as well as cell death. In murine macrophages (M Phi), stimulation of TLR3 and TLR4, but not TLR9, can cause HMGB1 translocation. With cell death, necrosis can lead to extracellular HMGB1 by a passive mechanism. With apoptosis, HMGB1 is only released during secondary necrosis, when cell permeability barriers break down. Since agents that stimulate M Phi can also induce apoptosis, HMGB1 release following TLR stimulation may also reflect a contribution from dead cells, suggesting a common mechanism for protein release in activation and death.
引用
收藏
页码:299 / 301
页数:3
相关论文
共 20 条
[1]
High mobility group 1 protein (HMG-1) stimulates proinflammatory cytokine synthesis in human monocytes [J].
Andersson, U ;
Wang, HC ;
Palmblad, K ;
Aveberger, AC ;
Bloom, O ;
Erlandsson-Harris, H ;
Janson, A ;
Kokkola, R ;
Zhang, MH ;
Yang, H ;
Tracey, KJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (04) :565-570
[2]
The extracellular release of HMGB1 during apoptotic cell death [J].
Bell, Charles W. ;
Jiang, Weiwen ;
Reich, Charles F., III ;
Pisetsky, David S. .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2006, 291 (06) :C1318-C1325
[3]
DAMPs, PAMPs and alarmins: all we need to know about danger [J].
Bianchi, Marco E. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2007, 81 (01) :1-5
[4]
Monocytic cells hyperacetylate chromatin protein HMGB1 to redirect it towards secretion [J].
Bonaldi, T ;
Talamo, F ;
Scaffidi, P ;
Ferrera, D ;
Porto, A ;
Bachi, A ;
Rubartelli, A ;
Agresti, A ;
Bianchi, ME .
EMBO JOURNAL, 2003, 22 (20) :5551-5560
[5]
The lack of chromosomal protein Hmg1 does not disrupt cell growth but causes lethal hypoglycaemia in newborn mice [J].
Calogero, S ;
Grassi, F ;
Aguzzi, A ;
Voigtländer, T ;
Ferrier, P ;
Ferrari, S ;
Bianchi, ME .
NATURE GENETICS, 1999, 22 (03) :276-280
[6]
FERRARI S, 1994, J BIOL CHEM, V269, P28803
[7]
The nuclear protein HMGB1 is secreted by monocytes via a non-classical, vesicle-mediated secretory pathway [J].
Gardella, S ;
Andrei, C ;
Ferrera, D ;
Lotti, LV ;
Torrisi, MR ;
Bianchi, ME ;
Rubartelli, A .
EMBO REPORTS, 2002, 3 (10) :995-1001
[8]
Goodwin G H, 1977, Methods Cell Biol, V16, P257
[9]
Post-translational methylation of high mobility group box 1 (HMGB1) causes its cytoplasmic localization in neutrophils [J].
Ito, Ichiaki ;
Fukazawa, Jutarou ;
Yoshida, Michiteru .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (22) :16336-16344
[10]
The relationship between apoptosis and high-mobility group protein 1 release from murine macrophages stimulated with lipopolysaccharide or polyinosinic-polycytidylic acid [J].
Jiang, Weiwen ;
Bell, Charles W. ;
Pisetsky, David S. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (10) :6495-6503