Annexin 1: more than an anti-phospholipase protein

被引:241
作者
Parente, L
Solito, E
机构
[1] Univ Salerno, Dept Pharmaceut Sci, I-84084 Salerno, Italy
[2] Univ London Imperial Coll Sci Technol & Med, Dept Neuroendocrinol, London, England
基金
英国惠康基金;
关键词
annexin; 1; glucocorticoids; inflammation; cell migration; apoptosis;
D O I
10.1007/s00011-003-1235-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Annexin 1 (ANXA1) is the first characterized member of the annexin family of proteins able to bind (i.e. to annex) to cellular membranes in a calcium-dependent manner. ANXA1 may be induced by glucocorticoids in inflammatory cells and shares with these drugs many anti-inflammatory effects. Originally described as a phospholipase A, (PLA(2))-inhibitory protein, ANXA1 can affect many components of the inflammatory reaction besides the metabolism of arachidonic acid. Recent data have shown that ANXA1 may specifically target cytosolic PLA(2) by both direct enzyme inhibition and suppression of cytokine-induced activation of the enzyme. ANXA1 inhibits the expression and/or activity of other inflammatory enzymes like inducible nitric oxide synthase (NOS) in macrophages and inducible cyclooxygenase (COX-2) in activated microglia. The inhibition of NOS expression may be caused by the stimulation of IL-10 release induced by ANXA1 in macrophages. Like glucocorticoids, ANXA1 exerts profound inhibitory effects on both neutrophil and monocyte migration in inflammation. Several mechanisms may contribute to the protein effect on cell migration, namely the activation of receptors like the formyl peptide receptor (FPR) and the lipoxin A(4) receptor (ALXR), the shedding of L-selectin, the binding to alpha(4)beta(1) integrin and carboxylated N-glycans. Furthermore, again mimicking the action of glucocorticoids, ANXA1 promotes inflammatory cell apoptosis associated with transient rise in intracellular calcium and caspase-3 activation. Finally, ANXA1 has been recently identified as one of the 'eat-me' signals on apoptotic cells to be recognised and ingested by phagocytes. Thus, ANXA1 may contribute to the anti-inflammatory signalling that allows safe post-apoptotic clearance of dead cells.
引用
收藏
页码:125 / 132
页数:8
相关论文
共 90 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]   Specific activation of the cysteine protease CPP32 during the negative selection of T cells in the thymus [J].
Alam, A ;
Braun, MY ;
Hartgers, F ;
Lesage, S ;
Cohen, L ;
Hugo, P ;
Denis, F ;
Sekaly, RP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (09) :1503-1512
[3]   The annexin protein lipocortin 1 regulates the MAPK/ERK pathway [J].
Alldridge, LC ;
Harris, HJ ;
Plevin, R ;
Hannon, R ;
Bryant, CE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (53) :37620-37628
[4]   Suppression of cytokine synthesis, integrin expression and chronic inflammation by inhibitors of cytosolic phospholipase A(2) [J].
AmandiBurgermeister, E ;
Tibes, U ;
Kaiser, BM ;
Friebe, WG ;
Scheuer, WV .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1997, 326 (2-3) :237-250
[5]   Annexin I is an endogenous ligand that mediates apoptotic cell engulfment [J].
Arur, S ;
Uche, UE ;
Rezaul, K ;
Fong, M ;
Scranton, V ;
Cowan, AE ;
Mohler, W ;
Han, DK .
DEVELOPMENTAL CELL, 2003, 4 (04) :587-598
[6]   Death receptors: Signaling and modulation [J].
Ashkenazi, A ;
Dixit, VM .
SCIENCE, 1998, 281 (5381) :1305-1308
[7]  
BOMALASKI JS, 1991, J IMMUNOL, V146, P3904
[8]   Lipopolysaccharide induces rapid production of IL-10 by monocytes in the presence of apoptotic neutrophils [J].
Byrne, A ;
Reen, DJ .
JOURNAL OF IMMUNOLOGY, 2002, 168 (04) :1968-1977
[9]  
CHAO CC, 1992, J IMMUNOL, V149, P2736
[10]   Activation of lipoxin A4 receptors by aspirin-triggered lipoxins and select peptides evokes ligand-specific responses in inflammation [J].
Chiang, N ;
Fierro, IM ;
Gronert, K ;
Serhan, CN .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (07) :1197-1207