Expression and function of serum amyloid A, a major acute-phase protein, in normal and disease states

被引:375
作者
Urieli-Shoval, S [1 ]
Linke, RP
Matzner, Y
机构
[1] Hadassah Univ Hosp, Hematol Unit, IL-91240 Jerusalem, Israel
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
关键词
D O I
10.1097/00062752-200001000-00012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Serum amyloid A (SAA), the precursor protein in inflammation-associated reactive amyloidosis (AA-type), is an acute phase reactant whose level in the blood increases in response to various insults, it is expressed in the liver, but its physiological role is not well understood. Recently, a broader view of SAA expression and function has been emerging. Expression studies show local production of SAA proteins in histologically normal, atherosclerotic, Alzheimer, inflammatory, and tumor tissues. Binding sites in the SAA protein for high density lipoproteins, calcium, laminin, and heparin/heparan-sulfate were described. Adhesion motifs were identified and new functions, affecting cell adhesion, migration, proliferation and aggregation have been described. These findings emphasize the importance of SAA in various physiological and pathological processes, including inflammation, atherosclerosis, thrombosis, AA-amyloidosis, rheumatoid arthritis, and neoplasia. In addition, recent experiments suggest that SAA may play a "housekeeping" role in normal human tissues. (C) 2000 Lippincott Williams & Wilkins, Inc.
引用
收藏
页码:64 / 69
页数:6
相关论文
共 71 条
[21]   Regulation of serum amyloid A protein expression during the acute-phase response [J].
Jensen, LE ;
Whitehead, AS .
BIOCHEMICAL JOURNAL, 1998, 334 :489-503
[22]   KINETIC MODELING AND MATHEMATICAL-ANALYSIS INDICATE THAT ACUTE-PHASE GENE-EXPRESSION IN HEP 3B CELLS IS REGULATED BY BOTH TRANSCRIPTIONAL AND POSTTRANSCRIPTIONAL MECHANISMS [J].
JIANG, SL ;
SAMOLS, D ;
RZEWNICKI, D ;
MACINTYRE, SS ;
GREBER, I ;
SIPE, J ;
KUSHNER, I .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (03) :1253-1261
[23]  
JIANG SL, 1995, J IMMUNOL, V154, P825
[24]  
KISILEVSKY R, 1992, LAB INVEST, V66, P778
[25]   A cell culture system for the study of amyloid pathogenesis - Amyloid formation by peritoneal macrophages cultured with recombinant serum amyloid A [J].
Kluve-Beckerman, B ;
Liepnieks, JJ ;
Wang, LS ;
Benson, MD .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (01) :123-133
[26]   NONEXPRESSION OF THE HUMAN SERUM AMYLOID-A 3 (SAA3) GENE [J].
KLUVEBECKERMAN, B ;
DRUMM, ML ;
BENSON, MD .
DNA AND CELL BIOLOGY, 1991, 10 (09) :651-661
[27]   Regulation of extrahepatic apolipoprotein serum amyloid a (ApoSAA) gene expression by interleukin-1 alpha alone: Synthesis and secretion of ApoSAA by cultured aortic smooth muscle cells [J].
Kumon, Y ;
Sipe, JD ;
Brinckerhoff, CE ;
Schreiber, BM .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1997, 46 (03) :284-291
[28]  
Kumon Y, 1997, J RHEUMATOL, V24, P14
[29]  
Kumon Y, 1999, J RHEUMATOL, V26, P785
[30]   IMMUNOLOGICAL STUDIES OF MAJOR NONIMMUNOGLOBULIN PROTEIN OF AMYLOID .1. IDENTIFICATION AND PARTIAL CHARACTERIZATION OF A RELATED SERUM COMPONENT [J].
LEVIN, M ;
PRAS, M ;
FRANKLIN, EC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1973, 138 (02) :373-380