利用 CARS 和双光子显微镜对肿瘤及其相关微环境进行活体成像。

IntraVital Pub Date : 2015-06-08 eCollection Date: 2015-01-01 DOI:10.1080/21659087.2015.1055430
Martin Lee, Andy Downes, You-Ying Chau, Bryan Serrels, Nick Hastie, Alistair Elfick, Valerie Brunton, Margaret Frame, Alan Serrels
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引用次数: 0

摘要

使用共焦和多光子显微镜进行体内癌症成像,有助于我们了解体内癌细胞的行为以及与周围肿瘤微环境的相互作用。然而,迄今为止的许多研究都依赖于使用荧光染料或基因编码探针,这些探针能对感兴趣的结构或细胞群进行可视化,但无法显示周围肿瘤微环境的复杂性。在这里,我们展示了结合双光子荧光和 CARS 的多模式显微镜可以开始解决这一不足,无需额外标记就能对肿瘤龛进行详细成像。这可以通过光学观察窗在活体肿瘤动物身上进行,允许对肿瘤龛内的动态过程进行实时和纵向成像。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In vivo imaging of the tumor and its associated microenvironment using combined CARS / 2-photon microscopy.

In vivo imaging of the tumor and its associated microenvironment using combined CARS / 2-photon microscopy.

In vivo imaging of the tumor and its associated microenvironment using combined CARS / 2-photon microscopy.

In vivo imaging of the tumor and its associated microenvironment using combined CARS / 2-photon microscopy.

The use of confocal and multi-photon microscopy for intra-vital cancer imaging has impacted on our understanding of cancer cell behavior and interaction with the surrounding tumor microenvironment in vivo. However, many studies to-date rely on the use fluorescent dyes or genetically encoded probes that enable visualization of a structure or cell population of interest, but do not illuminate the complexity of the surrounding tumor microenvironment. Here, we show that multi-modal microscopy combining 2-photon fluorescence with CARS can begin to address this deficit, enabling detailed imaging of the tumor niche without the need for additional labeling. This can be performed on live tumor-bearing animals through optical observation windows, permitting real-time and longitudinal imaging of dynamic processes within the tumor niche.

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