Annexins I and IV inhibit Staphylococcus aureus attachment to human macrophages

被引:19
作者
Gotoh, M
Takamoto, Y
Kurosaka, K
Masuda, J
Ida, M
Satoh, A
Takayamac, E
Kojima-Aikawa, K
Kobayashi, Y
Matsumoto, I
机构
[1] Ochanomizu Univ, Grad Sch Humanities & Sci, Bunkyo Ku, Tokyo 1128610, Japan
[2] Toho Univ, Fac Sci, Lab Mol Immunol, Funabashi, Chiba 2748510, Japan
[3] Natl Def Med Coll, Dept Parasitol, Tokorozawa, Saitama 3598513, Japan
关键词
annexins; lipoteichoic acid; anti-inflammatory; Gram-positive bacteria;
D O I
10.1016/j.imlet.2004.12.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Annexins are a family of proteins that bind to phospholipids and carbohydrates in a calcium-dependent manner. They are present in a variety of body fluids. Previous studies have shown that annexins have anti-inflammatory activities for lipid A of Gram-negative bacteria. The present study investigated the effect of annexins on interaction between Gram-positive bacteria and immune cells such as macrophages. Annexins I and IV bound to lipoteichoic acids which are surface molecules on Gram-positive bacteria. Binding of annexins I and IV to whole Staphylococcus aureus (S. aureus) were observed and these bindings were inhibited by lipoteichoic acid from S. aureus. Moreover, annexins I and IV suppressed the attachment of S. aureus to phorbol 12-myristate 13-acetate-treated THP-1 cells (human macrophages). These results suggest that annexins I and IV have ligand specificities toward foreign substances, and that the annexins might have some anti-inflammatory property for Gram-positive bacteria. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:297 / 302
页数:6
相关论文
共 38 条
[1]   Neutrophil accumulation induced by bacterial lipopolysaccharide: effects of dexamethasone and annexin 1 [J].
Allcock, GH ;
Allegra, M ;
Flower, RJ ;
Perretti, M .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2001, 123 (01) :62-67
[2]   CORTICOSTEROIDS INCREASE LIPOCORTIN-I IN BAL FLUID FROM NORMAL INDIVIDUALS AND PATIENTS WITH LUNG-DISEASE [J].
AMBROSE, MP ;
HUNNINGHAKE, GW .
JOURNAL OF APPLIED PHYSIOLOGY, 1990, 68 (04) :1668-1671
[3]   Involvement of phosphatidylserine exposure in the recognition and phagocytosis of uremic erythrocytes [J].
Bonomini, M ;
Sirolli, V ;
Reale, M ;
Arduini, A .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 37 (04) :807-814
[4]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[5]  
CHRISTMAS P, 1991, J BIOL CHEM, V266, P2499
[6]  
COUPADE C, 2001, AM J PATHOL, V159, P1435
[7]   LIPOCORTIN-1 MEDIATES DEXAMETHASONE-INDUCED GROWTH ARREST OF THE A549 LUNG ADENOCARCINOMA CELL-LINE [J].
CROXTALL, JD ;
FLOWER, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (08) :3571-3575
[8]  
Eberhard DA, 1998, BIOCHEM J, V330, P67
[9]   A receptor for phosphatidylserine-specific clearance of apoptotic cells [J].
Fadok, VA ;
Bratton, DL ;
Rose, DM ;
Pearson, A ;
Ezekewitz, RAB ;
Henson, PM .
NATURE, 2000, 405 (6782) :85-90
[10]   The role of phosphatidylserine in recognition of apoptotic cells by phagocytes [J].
Fadok, VA ;
Bratton, DL ;
Frasch, SC ;
Warner, ML ;
Henson, PM .
CELL DEATH AND DIFFERENTIATION, 1998, 5 (07) :551-562