A Novel High-resolution In vivo Imaging Technique to Study the Dynamic Response of Intracranial Structures to Tumor Growth and Therapeutics

被引:14
作者
Burrell, Kelly [1 ]
Agnihotri, Sameer [1 ]
Leung, Michael [2 ]
DaCosta, Ralph [2 ]
Hill, Richard [2 ]
Zadeh, Gelareh [3 ]
机构
[1] Hosp Sick Children, Brain Tumor Res Ctr, Toronto, ON, Canada
[2] Princess Margaret Hosp, Ontario Canc Inst, Toronto, ON, Canada
[3] Toronto Western Hosp, Toronto, ON, Canada
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2013年 / 76期
关键词
Cancer Biology; Issue; 76; Medicine; Biomedical Engineering; Cellular Biology; Molecular Biology; Genetics; Neuroscience; Neurobiology; Biophysics; Anatomy; Physiology; Surgery; Intracranial Window; In vivo imaging; Stereotactic radiation; Bone Marrow Derived Cells; confocal microscopy; two-photon microscopy; drug-cell interactions; drug kinetics; brain; imaging; tumors; animal model; MARROW-DERIVED CELLS; LONG-TERM; ANGIOGENESIS; PRECURSORS; CONTRIBUTE; REVEALS;
D O I
10.3791/50363
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have successfully integrated previously established Intracranial window (ICW) technology (1-4) with intravital 2-photon confocal microscopy to develop a novel platform that allows for direct long-term visualization of tissue structure changes intracranially. Imaging at a single cell resolution in a real-time fashion provides supplementary dynamic information beyond that provided by standard end-point histological analysis, which looks solely at 'snap-shot' cross sections of tissue. Establishing this intravital imaging technique in fluorescent chimeric mice, we are able to image four fluorescent channels simultaneously. By incorporating fluorescently labeled cells, such as GFP+ bone marrow, it is possible to track the fate of these cells studying their long-term migration, integration and differentiation within tissue. Further integration of a secondary reporter cell, such as an mCherry glioma tumor line, allows for characterization of cell: cell interactions. Structural changes in the tissue microenvironment can be highlighted through the addition of intra-vital dyes and antibodies, for example CD31 tagged antibodies and Dextran molecules. Moreover, we describe the combination of our ICW imaging model with a small animal micro-irradiator that provides stereotactic irradiation, creating a platform through which the dynamic tissue changes that occur following the administration of ionizing irradiation can be assessed. Current limitations of our model include penetrance of the microscope, which is limited to a depth of up to 900 mu m from the sub cortical surface, limiting imaging to the dorsal axis of the brain. The presence of the skull bone makes the ICW a more challenging technical procedure, compared to the more established and utilized chamber models currently used to study mammary tissue and fat pads (5-7). In addition, the ICW provides many challenges when optimizing the imaging.
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页数:13
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