Development of magnetic resonance imaging contrast material for in vivo mapping of tissue transglutaminase activity

被引:27
作者
Mazooz, G
Mehlman, T
Lai, TS
Greenberg, CS
Dewhirst, MW
Neeman, M [1 ]
机构
[1] Weizmann Inst Sci, Dept Regulat Biol, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Biol Serv, IL-76100 Rehovot, Israel
[3] Duke Univ, Med Ctr, Dept Med, Durham, NC USA
[4] Duke Univ, Med Ctr, Dept Radiol Oncol, Durham, NC USA
关键词
D O I
10.1158/0008-5472.CAN-04-2269
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Transglutaminases are a family of enzymes that play an important role in tissue remodeling by catalyzing covalent cross-links between proteins of the extracellular matrix. Elevated activity of transglutaminase was shown at the boundaries of invading tumors, in association with angiogenesis, in stabilization of atherosclerotic plaques, and in generation of blood clots. The aim of this work was to develop a low molecular weight substrate of transglutaminase that could serve for noninvasive magnetic resonance and optical mapping of transglutaminase-mediated cross-linking activity. A 2 kDa contrast material was generated which showed cross-linking by either tissue transglutaminase or factor XIII in the context of multicellular tumor spheroids or fibrin clots, respectively. Successful detection by nuclear magnetic resonance microscopy of transglutaminase-mediated cross-linking of the contrast material to MCF7 multicellular spheroids provides hope that this approach could potentially be developed for clinical demarcation of sites of transglutaminase activity.
引用
收藏
页码:1369 / 1375
页数:7
相关论文
共 25 条
[1]  
ACHYUTHAN KE, 1987, J BIOL CHEM, V262, P1901
[2]  
AESCHLIMANN D, 1994, THROMB HAEMOSTASIS, V71, P402
[3]   Thrombin upregulates tissue transglutaminase in endothelial cells - A potential role for tissue transglutaminase in stability of atherosclerotic plaque [J].
Auld, GC ;
Ritchie, H ;
Robbie, LA ;
Booth, NA .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (10) :1689-1694
[4]   First soluble M@C60 derivatives provide enhanced access to metallofullerenes and permit in vivo evaluation of Gd@C60[C(COOH)2]10 as a MRI contrast agent [J].
Bolskar, RD ;
Benedetto, AF ;
Husebo, LO ;
Price, RE ;
Jackson, EF ;
Wallace, S ;
Wilson, LJ ;
Alford, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (18) :5471-5478
[5]   Modulation of the pharmacokinetics of macromolecular contrast material by avidin chase: MRI, optical, and inductively coupled plasma mass spectrometry tracking of triply labeled albumin [J].
Dafni, H ;
Gilead, A ;
Nevo, N ;
Eilam, R ;
Harmelin, A ;
Neeman, M .
MAGNETIC RESONANCE IN MEDICINE, 2003, 50 (05) :904-914
[6]  
Dafni H, 2002, CANCER RES, V62, P6731
[7]  
Denko NC, 2001, CANCER RES, V61, P795
[8]  
FOLK JE, 1977, ADV PROTEIN CHEM, P311
[9]   Tissue transglutaminase is an important player at the surface of human endothelial cells:: Evidence for its externalization and its colocalization with the β1 integrin [J].
Gaudry, CA ;
Verderio, E ;
Jones, RA ;
Smith, C ;
Griffin, M .
EXPERIMENTAL CELL RESEARCH, 1999, 252 (01) :104-113
[10]   Transglutaminases: Nature's biological glues [J].
Griffin, M ;
Casadio, R ;
Bergamini, CM .
BIOCHEMICAL JOURNAL, 2002, 368 :377-396