Chemoattractants, extracellular proteases, and the integrated host defense response

被引:108
作者
Zabel, Brian A.
Zuniga, Luis
Ohyama, Takao
Allen, Samantha J.
Cichy, Joanna
Handel, Tracy M.
Butcher, Eugene C.
机构
[1] Vet Affairs Palo Alto Hlth Care Syst, Ctr Mol Biol & Med, Palo Alto, CA 94304 USA
[2] Stanford Univ, Sch Med, Dept Pathol, Lab Immunol & Vasc Biol, Stanford, CA 94305 USA
[3] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
[4] Jagiellonian Univ, Fac Biotechnol, PL-30387 Krakow, Poland
关键词
D O I
10.1016/j.exphem.2006.05.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The host response to tissue injury and/or infection is dependent on the action of numerous extracellular proteases. Proteolytic cascades trigger blood clotting, fibrinolysis, and complement activation, while proteases released upon leukocyte degranulation are integral to the processes of inflammation and immunity. Modulation of effector protein activity by proteases provides a critical layer of posttranslational control that enables rapid enzymatic regulation of target proteins. This report reviews the emerging literature describing a novel class of proteolytic targets, leukocyte chemoattractants, and, in particular, chemerin, a dendritic cell and macrophage chemoattractant activated by serine proteases of the coagulation, fibrinolytic, and inflammatory cascades. As chemoattractants are critical for both systemic leukocyte positioning by triggering integrin activation and subsequent recruitment from circulation, and local intratissue leukocyte positioning via chemotaxis, modulation of attractant activities by proteases may have profound effects on the immune response. (c) 2006 International Society for Experimental Hematology. Published by Elsevier Inc.
引用
收藏
页码:1021 / 1032
页数:12
相关论文
共 97 条
[11]  
CLARKLEWIS I, 1991, J BIOL CHEM, V266, P23128
[12]   STRUCTURE-ACTIVITY-RELATIONSHIPS OF CHEMOKINES [J].
CLARKLEWIS, I ;
KIM, KS ;
RAJARATHNAM, K ;
GONG, JH ;
DEWALD, B ;
MOSER, B ;
BAGGIOLINI, M ;
SYKES, BD .
JOURNAL OF LEUKOCYTE BIOLOGY, 1995, 57 (05) :703-711
[13]   Eotaxin is specifically cleaved by hookworm metalloproteases preventing its action in vitro and in vivo [J].
Culley, FJ ;
Brown, A ;
Conroy, DM ;
Sabroe, I ;
Pritchard, DI ;
Williams, TJ .
JOURNAL OF IMMUNOLOGY, 2000, 165 (11) :6447-6453
[14]   Local chemokine paralysis, a novel pathogenic mechanism for Porphyromonas gingivalis [J].
Darveau, RP ;
Belton, CM ;
Reife, RA ;
Lamont, RJ .
INFECTION AND IMMUNITY, 1998, 66 (04) :1660-1665
[15]   Identification of carboxypeptidase N as an enzyme responsible for C-terminal cleavage of stromal cell-derived factor-1α in the circulation [J].
Davis, DA ;
Singer, KE ;
Sierra, MD ;
Narazaki, M ;
Yang, FQ ;
Fales, HM ;
Yarchoan, R ;
Tosato, G .
BLOOD, 2005, 105 (12) :4561-4568
[16]  
Delgado MB, 2001, EUR J IMMUNOL, V31, P699, DOI 10.1002/1521-4141(200103)31:3<699::AID-IMMU699>3.0.CO
[17]  
2-6
[18]   Proteinaceous cysteine protease inhibitors [J].
Dubin, G .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2005, 62 (06) :653-669
[19]   Specific C-terminal cleavage and inactivation of interleukin-8 by invasive disease isolates of Streptococcus pyogenes [J].
Edwards, RJ ;
Taylor, GW ;
Ferguson, M ;
Murray, S ;
Rendell, N ;
Wrigley, A ;
Bai, ZH ;
Boyle, J ;
Finney, SJ ;
Jones, A ;
Russell, HH ;
Turner, C ;
Cohen, J ;
Faulkner, L ;
Sriskandan, S .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (05) :783-790
[20]   LIMITED AND DEFINED TRUNCATION AT THE C-TERMINUS ENHANCES RECEPTOR-BINDING AND DEGRANULATION ACTIVITY OF THE NEUTROPHIL-ACTIVATING PEPTIDE-2 (NAP-2) - COMPARISON OF NATIVE AND RECOMBINANT NAP-2 VARIANTS [J].
EHLERT, JE ;
PETERSEN, F ;
KUBBUTAT, MHG ;
GERDES, J ;
FLAD, HD ;
BRANDT, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (11) :6338-6344