S100A8: emerging functions and regulation

被引:113
作者
Passey, RJ
Xu, K
Hume, DA
Geczy, CL [1 ]
机构
[1] Univ New S Wales, Sch Pathol, Cytokine Res Unit, Sydney, NSW 2052, Australia
[2] Univ Queensland, Dept Biochem, St Lucia, Qld 4067, Australia
[3] Univ Queensland, Dept Microbiol, St Lucia, Qld 4067, Australia
[4] Univ Queensland, Ctr Cellular & Mol Biol, St Lucia, Qld 4067, Australia
关键词
chemotaxis; inflammation; expression; embryogenesis; differentiation; development;
D O I
10.1002/jlb.66.4.549
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The functional importance of members of the S100 Ca2+-binding protein family is becoming apparent. Murine (m)S100A8 (initially named CP-10) is a potent chemoattractant (10(-13) to 10(-11) M) for myeloid cells and the chemotactic activity of other S100s has since been reported, suggesting a new class of chemoattractants. Murine S100A8 has been associated with a number of acute and chronic inflammatory conditions including bacterial infection, atherogenesis, and cystic fibrosis, It is expressed constitutively with S100A9 in neutrophils and is regulated by inflammatory stimulants in macrophages and microvascular endothelial cells. The lack of co-expression of S100A9 with S100A8 in activated macrophages suggests distinct functions for the proteins expressed by different cell types. Glucocorticoids up-regulate induction of mS100A8 by inflammatory mediators, and its exquisite sensitivity to oxidation suggests that it may protect against oxidative tissue damage, Inactivation of the mS100A8 gene is embryonic lethal, providing the first evidence for non-redundant function of a member of the S100 gene family, S100A8 may have au immunoregulatory role by contributing to the regulation of fetal-maternal interactions. It may play a protective role and its absence may allow infiltration by maternal cells, a process eventually manifesting as resorption, This review focuses on the variety of emerging functions attributed to murine S100A8, a protein implicated in embryogenesis, growth, differentiation, and immune and inflammatory processes.
引用
收藏
页码:549 / 556
页数:8
相关论文
共 93 条
[71]   EXPRESSION AND REGULATION OF TUMOR-NECROSIS-FACTOR IN MACROPHAGES FROM CYSTIC-FIBROSIS PATIENTS [J].
PFEFFER, KD ;
HUECKSTEADT, TP ;
HOIDAL, JR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1993, 9 (05) :511-519
[72]   Identification of noncovalent dimeric complexes of the recombinant murine S100 protein CP10 by electrospray ionization mass spectrometry and chemical cross-linking [J].
Raftery, MJ ;
Geczy, CL .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1998, 9 (05) :533-539
[73]   Isolation of the murine S100 protein MRP14 (14 kDa migration-inhibitory-factor-related protein) from activated spleen cells: Characterization of post-translational modifications and zinc binding [J].
Raftery, MJ ;
Harrison, CA ;
Alewood, P ;
Jones, A ;
Geczy, CL .
BIOCHEMICAL JOURNAL, 1996, 316 :285-293
[74]  
Rammes A, 1997, J BIOL CHEM, V272, P9496
[75]   INCREASED COEXPRESSION OF CFTR AND S100 CALCIUM-BINDING PROTEINS MRP8 AND MRP14 MESSENGER-RNAS IN CYSTIC-FIBROSIS HUMAN TRACHEAL GLAND-CELLS [J].
RENAUD, W ;
MERTEN, M ;
FIGARELLA, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 201 (03) :1518-1525
[76]  
RIORDAN JR, 1989, SCIENCE, V245, P1066
[77]   EXPRESSION OF THE CALCIUM-BINDING PROTEINS MRP8 AND MRP14 IN MONOCYTES IS REGULATED BY A CALCIUM-INDUCED SUPPRESSOR MECHANISM [J].
ROTH, J ;
GOEBELER, M ;
WROCKLAGE, V ;
VANDENBOS, C ;
SORG, C .
BIOCHEMICAL JOURNAL, 1994, 301 :655-660
[78]   The fatty acid-binding heterocomplex FA-p34 formed by S100A8 and S100A9 is the major fatty acid carrier in neutrophils and translocates from the cytosol to the membrane upon stimulation [J].
Roulin, K ;
Hagens, G ;
Hotz, R ;
Saurat, JH ;
Veerkamp, JH ;
Siegenthaler, G .
EXPERIMENTAL CELL RESEARCH, 1999, 247 (02) :410-421
[79]   COAGULATION AND THE EXPRESSION OF CELL-MEDIATED-IMMUNITY [J].
RYAN, J ;
GECZY, C .
IMMUNOLOGY AND CELL BIOLOGY, 1987, 65 :127-139
[80]  
SARIS CJM, 1987, J BIOL CHEM, V262, P10663