Proteolysis and Toxoplasma invasion

被引:37
作者
Carruthers, Vern B. [1 ]
机构
[1] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, W Harry Feinstone Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
关键词
protease; propeptide; processing; invasion; microneme; rhoptry;
D O I
10.1016/j.ijpara.2006.02.008
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Apicomplexan parasites including Toxoplasma gondii cause wct idespread human and animal diseases, often with the most severe manifestations involving the central nervous system. The need for new therapeutic agents along with the fascinating biology of these parasites has fueled a keen interest in understanding how key steps in the life cycle are regulated. Proteolysis is intimately associated with cell and tissue invasion by these obligate intracellular parasites and recent studies have begun to identify the proteases involved in these processes. Based on clues from inhibitor experiments and cleavage site mapping studies, several groups are using emerging genome information, chemical proteomics and molecular genetics to identify and validate proteases that regulate secretory organelle biogenesis and invasion protein activity. These studies are revealing roles for an assortment of proteases including cathepsins, subtilases and rhomboids in cell and tissue invasion. The identification of highly selective inhibitors for these proteases has the potential to not only further dissect their roles in infection but also to ameliorate disease. (c) 2006 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:595 / 600
页数:6
相关论文
共 48 条
[1]   CHARACTERIZATION OF MICRONEME PROTEINS OF TOXOPLASMA-GONDII [J].
ACHBAROU, A ;
MERCEREAUPUIJALON, O ;
AUTHEMAN, JM ;
FORTIER, B ;
CAMUS, D ;
DUBREMETZ, JF .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1991, 47 (02) :223-233
[2]   THE EFFECT OF PROTEASE INHIBITORS ON EIMERIA-VERMIFORMIS INVASION OF CULTURED-CELLS [J].
ADAMS, JH ;
BUSHELL, GR .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1988, 18 (05) :683-685
[3]   Identification of the moving junction complex of Toxoplasma gondii:: A collaboration between distinct secretory organelles [J].
Alexander, David L. ;
Mital, Jeffrey ;
Ward, Gary E. ;
Bradley, Peter ;
Boothroyd, John C. .
PLOS PATHOGENS, 2005, 1 (02) :137-149
[4]   Transepithelial migration of Toxoplasma gondii involves an interaction of intercellular adhesion molecule 1 (ICAM-1) with the parasite adhesin MIC2 [J].
Barragan, A ;
Brossier, F ;
Sibley, LD .
CELLULAR MICROBIOLOGY, 2005, 7 (04) :561-568
[5]   A GFP-based motif-trap reveals a novel mechanism of targeting for the Toxoplasma ROP4 protein [J].
Bradley, PJ ;
Li, N ;
Boothroyd, JC .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2004, 137 (01) :111-120
[6]   Unprocessed Toxoplasma ROP1 is effectively targeted and secreted into the nascent parasitophorous vacuole [J].
Bradley, PJ ;
Hsieh, CL ;
Boothroyd, JC .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2002, 125 (1-2) :189-193
[7]   The pro region of Toxoplasma ROP1 is a rhoptry-targeting signal [J].
Bradley, PJ ;
Boothroyd, JC .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2001, 31 (11) :1177-1186
[8]   A spatially localized rhomboid protease cleaves cell surface adhesins essential for invasion by Toxoplasma [J].
Brossier, F ;
Jewett, TJ ;
Sibley, LD ;
Urban, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (11) :4146-4151
[9]   C-terminal processing of the toxoplasma protein MIC2 is essential for invasion into host cells [J].
Brossier, F ;
Jewettt, TJ ;
Lovett, JL ;
Sibley, LD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :6229-6234
[10]   Regulated intramembrane proteolysis: A control mechanism conserved from bacteria to humans [J].
Brown, MS ;
Ye, J ;
Rawson, RB ;
Goldstein, JL .
CELL, 2000, 100 (04) :391-398