Techniques: Intravital microscopy - a method for investigating disseminated intravascular coagulation?

被引:12
作者
Norman, K [1 ]
机构
[1] Univ Sheffield, Ctr Clin Sci, No Gen Hosp, Cardiovasc Res Unit, Sheffield S5 7AU, S Yorkshire, England
基金
英国惠康基金;
关键词
D O I
10.1016/j.tips.2005.04.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Intravital microscopy (IVM) enables the study of cellular and molecular events in living organisms. Confocal microscopy permits images to be collected from narrow focal planes without interference from out-of-focus regions, and multi-photon microscopy produces high-resolution images from deep (several hundred micrometers) within opaque organs and tissues. Lasers that are targeted through microscope objectives can injure individual microvessels and induce thrombi that can be studied in detail. The marriage of these technologies provides exciting possibilities for investigating the inflammation and coagulation that is associated with disseminated intravascular coagulation (DIC). In this review, I consider some of the new technology associated with microscopy, give examples of discoveries that have been made using this technology and speculate on how the study of DIC might be advanced using IVM.
引用
收藏
页码:327 / 332
页数:6
相关论文
共 35 条
[1]   Disseminated intravascular coagulation - Current concepts of etiology, pathophysiology, diagnosis, and treatment [J].
Bick, RL .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 2003, 17 (01) :149-+
[2]  
BOTTCHER D, 1973, BEITR PATHOL, V149, P121
[3]   Endogenous nitric oxide protects against thromboembolism in venules but not in arterioles [J].
Broeders, MAW ;
Tangelder, GJ ;
Slaaf, DW ;
Reneman, RS ;
Egbrink, MGAO .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (01) :139-145
[4]   SHWARTZMAN REACTION [J].
BROZNA, JP .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1990, 16 (04) :326-332
[5]  
Carmeliet P, 1997, AM J PATHOL, V150, P761
[6]   A novel method for isolation of neutrophils from murine blood using negative immunomagnetic separation [J].
Cotter, MJ ;
Norman, KE ;
Hellewell, PG ;
Ridger, VC .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (02) :473-481
[7]   A mouse model of severe von Willebrand disease:: Defects in hemostasis and thrombosis [J].
Denis, C ;
Methia, N ;
Frenette, PS ;
Rayburn, H ;
Ullman-Culleré, M ;
Hynes, RO ;
Wagner, DD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) :9524-9529
[8]   Accumulation of tissue factor into developing thrombi in vivo is dependent upon microparticle P-selectin glycoprotein ligand 1 and platelet P-selectin [J].
Falati, S ;
Liu, QD ;
Gross, P ;
Merrill-Skoloff, G ;
Chou, J ;
Vandendries, E ;
Celi, A ;
Croce, K ;
Furie, BC ;
Furie, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (11) :1585-1598
[9]   Real-time in vivo imaging of platelets, tissue factor and fibrin during arterial thrombus formation in the mouse [J].
Falati, S ;
Gross, P ;
Merrill-Skoloff, G ;
Furie, BC ;
Furie, B .
NATURE MEDICINE, 2002, 8 (10) :1175-1180
[10]   Role of platelet P-selectin and microparticle PSGL-1 in thrombus formation [J].
Furie, B ;
Furie, BC .
TRENDS IN MOLECULAR MEDICINE, 2004, 10 (04) :171-178