Application of intravital microscopy in studies of tumor microcirculation

被引:25
作者
Lunt, Sarah Jane [1 ,2 ]
Gray, Colin [3 ]
Reyes-Aldasoro, Constantino Carlos [1 ,2 ]
Matcher, Stephen J. [4 ]
Tozer, Gillian M. [1 ,2 ]
机构
[1] Univ Sheffield, Dept Oncol, Sch Med, Sheffield S10 2RX, S Yorkshire, England
[2] Univ Sheffield, Tumour Microcirculat Grp, Sch Med, Sheffield S10 2RX, S Yorkshire, England
[3] Univ Sheffield, Dept Cardiovasc Sci, Sch Med, Sheffield S10 2RX, S Yorkshire, England
[4] Univ Sheffield, Kroto Inst, Sheffield S3 7HQ, S Yorkshire, England
关键词
intravital microscopy; optical imaging; window chamber; tumor microcirculation; angiogenesis; vascular targeting; OPTICAL COHERENCE TOMOGRAPHY; ENDOTHELIAL GROWTH-FACTOR; GREEN FLUORESCENT PROTEIN; LASER-SCANNING MICROSCOPY; BLOOD-VESSEL MATURATION; IN-VIVO; VASCULAR-PERMEABILITY; NEOPLASTIC TISSUES; WINDOW CHAMBER; QUANTUM DOTS;
D O I
10.1117/1.3281674
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To grow and progress, solid tumors develop a vascular network through co-option and angiogenesis that is characterized by multiple structural and functional abnormalities, which negatively influence therapeutic outcome through direct and indirect mechanisms. As such, the morphology and function of tumor blood vessels, plus their response to different treatments, are a vital and active area of biological research. Intravital microscopy (IVM) has played a key role in studies of tumor angiogenesis, and ongoing developments in molecular probes, imaging techniques, and postimage analysis methods have ensured its continued and widespread use. In this review we discuss some of the primary advantages and disadvantages of IVM approaches and describe recent technological advances in optical microscopy (e.g., confocal microscopy, multiphoton microscopy, hyperspectral imaging, and optical coherence tomography) with examples of their application to studies of tumor angiogenesis. (C) 2010 Society of Photo-Optical Instrumentation Engineers. [DOI: 10.1117/1.3281674]
引用
收藏
页数:14
相关论文
共 141 条
[1]   Automated tracing and change analysis of angiogenic vasculature from in vivo multiphoton confocal image time series [J].
Abdul-Karim, MA ;
Al-Kofahi, K ;
Brown, EB ;
Jain, RK ;
Roysam, B .
MICROVASCULAR RESEARCH, 2003, 66 (02) :113-125
[2]   Dynamic imaging of cancer growth and invasion: a modified skin-fold chamber model [J].
Alexander, Stephanie ;
Koehl, Gudrun E. ;
Hirschberg, Markus ;
Geissler, Edward K. ;
Friedl, Peter .
HISTOCHEMISTRY AND CELL BIOLOGY, 2008, 130 (06) :1147-1154
[3]  
Algire GH, 1943, JNCI-J NATL CANCER I, V4, P1
[4]   An optical marker based on the UV-induced green-to-red photoconversion of a fluorescent protein [J].
Ando, R ;
Hama, H ;
Yamamoto-Hino, M ;
Mizuno, H ;
Miyawaki, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12651-12656
[5]   Regulated fast nucleocytoplasmic shuttling observed by reversible protein highlighting [J].
Ando, R ;
Mizuno, H ;
Miyawaki, A .
SCIENCE, 2004, 306 (5700) :1370-1373
[6]   Photoswitchable fluorescent proteins enable monochromatic multilabel imaging and dual color fluorescence nanoscopy [J].
Andresen, Martin ;
Stiel, Andre C. ;
Foelling, Jonas ;
Wenzel, Dirk ;
Schoenle, Andreas ;
Egner, Alexander ;
Eggeling, Christian ;
Hell, Stefan W. ;
Jakobs, Stefan .
NATURE BIOTECHNOLOGY, 2008, 26 (09) :1035-1040
[7]  
ASAISHI K, 1981, CANCER RES, V41, P1898
[8]   Abnormalities of basement membrane on blood vessels and endothelial sprouts in tumors [J].
Baluk, P ;
Morikawa, S ;
Haskell, A ;
Mancuso, M ;
McDonald, DM .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (05) :1801-1815
[9]   Semi-automated software for the three-dimensional delineation of complex vascular networks [J].
Barber, PR ;
Vojnovic, B ;
Ameer-Beg, SM ;
Hodgkiss, RJ ;
Tozer, GM ;
Wilson, J .
JOURNAL OF MICROSCOPY, 2003, 211 :54-62
[10]   TRANSPORT OF FLUID AND MACROMOLECULES IN TUMORS .1. ROLE OF INTERSTITIAL PRESSURE AND CONVECTION [J].
BAXTER, LT ;
JAIN, RK .
MICROVASCULAR RESEARCH, 1989, 37 (01) :77-104