α2-macroglobulin:: an evolutionarily conserved arm of the innate immune system

被引:251
作者
Armstrong, PB
Quigley, JP
机构
[1] Marine Biol Lab, Woods Hole, MA 02543 USA
[2] Univ Calif Davis, Dept Mol & Cellular Biol, Davis, CA 95616 USA
[3] SUNY Stony Brook, Sch Med, Dept Pathol, Stony Brook, NY 11794 USA
基金
美国国家科学基金会;
关键词
protease; protease inhibitor; alpha(2)-macroglobulin; Limulus; Horseshoe crab;
D O I
10.1016/S0145-305X(99)00018-X
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
All animals and plants have immune systems that protect them from the diversity of pathogens that would otherwise threaten their survival. The different components of the immune system may inactivate the pathogens themselves or promote the inactivation and clearance of toxic products produced by the pathogens, An important category of virulence factors of bacterial and prokaryotic pathogens are the proteases, which act to facilitate the invasion of the pathogens and to promote their destructive growth in the host organism. The present review concentrates on the comparative biology of an evolutionarily conserved arm of the immune system, the protein, alpha(2)-macroglobulin. alpha(2)-Macroglobulin is an abundant protein of the plasma of vertebrates and members of several invertebrate phyla and functions as a broad-spectrum protease-binding protein. Protease-conjugated alpha(2)-macroglobulin is selectively bound by cells contacting the body fluids and alpha(2)-macroglobulin and its protease cargo are then internalized and degraded in secondary lysosomes of those cells. In addition to this function as an agent for protease clearance, alpha(2)-macroglobulin binds a variety of other ligands, including several peptide growth factors and modulates the activity of a lectin-dependent cytolytic pathway in arthropods. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:375 / 390
页数:16
相关论文
共 95 条
[51]   PURIFICATION OF THE HUMAN PLACENTAL ALPHA-2-MACROGLOBULIN RECEPTOR [J].
JENSEN, PH ;
MOESTRUP, SK ;
GLIEMANN, J .
FEBS LETTERS, 1989, 255 (02) :275-280
[52]   THIOL REDUCTION OF HUMAN ALPHA2-MACROGLOBULIN - SUBUNIT STRUCTURE [J].
JONES, JM ;
CREETH, JM ;
KEKWICK, RA .
BIOCHEMICAL JOURNAL, 1972, 127 (01) :187-+
[53]   HEN EGG-WHITE OVOMACROGLOBULIN HAS A PROTEASE INHIBITORY ACTIVITY [J].
KITAMOTO, T ;
NAKASHIMA, M ;
IKAI, A .
JOURNAL OF BIOCHEMISTRY, 1982, 92 (05) :1679-1682
[54]   STRUCTURES AND FUNCTIONS OF MULTILIGAND LIPOPROTEIN RECEPTORS - MACROPHAGE SCAVENGER RECEPTORS AND LDL RECEPTOR-RELATED PROTEIN (LRP) [J].
KRIEGER, M ;
HERZ, J .
ANNUAL REVIEW OF BIOCHEMISTRY, 1994, 63 :601-637
[55]   EVIDENCE THAT THE NEWLY CLONED LOW-DENSITY-LIPOPROTEIN RECEPTOR RELATED PROTEIN (LRP) IS THE ALPHA-2-MACROGLOBULIN RECEPTOR [J].
KRISTENSEN, T ;
MOESTRUP, SK ;
GLIEMANN, J ;
BENDTSEN, L ;
SAND, O ;
SOTTRUPJENSEN, L .
FEBS LETTERS, 1990, 276 (1-2) :151-155
[56]   PROTEIN INHIBITORS OF PROTEINASES [J].
LASKOWSKI, M ;
KATO, I .
ANNUAL REVIEW OF BIOCHEMISTRY, 1980, 49 :593-626
[57]  
LAW SKA, 1988, COMPLEMENT
[58]   CRAYFISH ALPHA-MACROGLOBULIN AND 76 KDA PROTEIN - THEIR BIOSYNTHESIS AND SUBCELLULAR-LOCALIZATION OF THE 76 KDA PROTEIN [J].
LIANG, ZC ;
LINDBLAD, P ;
BEAUVAIS, A ;
JOHANSSON, MW ;
LATGE, JP ;
HALL, M ;
CERENIUS, L ;
SODERHALL, K .
JOURNAL OF INSECT PHYSIOLOGY, 1992, 38 (12) :987-995
[59]   THE PROTEASES AND PATHOGENICITY OF PARASITIC PROTOZOA [J].
MCKERROW, JH ;
SUN, E ;
ROSENTHAL, PJ ;
BOUVIER, J .
ANNUAL REVIEW OF MICROBIOLOGY, 1993, 47 :821-853
[60]   ALPHA(2)-MACROGLOBULIN-MEDIATED CLEARANCE OF PROTEASES FROM THE PLASMA OF THE AMERICAN HORSESHOE-CRAB, LIMULUS-POLYPHEMUS [J].
MELCHIOR, R ;
QUIGLEY, JP ;
ARMSTRONG, PB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (22) :13496-13502