Martin Lee, Andy Downes, You-Ying Chau, Bryan Serrels, Nick Hastie, Alistair Elfick, Valerie Brunton, Margaret Frame, Alan Serrels
{"title":"In vivo imaging of the tumor and its associated microenvironment using combined CARS / 2-photon microscopy.","authors":"Martin Lee, Andy Downes, You-Ying Chau, Bryan Serrels, Nick Hastie, Alistair Elfick, Valerie Brunton, Margaret Frame, Alan Serrels","doi":"10.1080/21659087.2015.1055430","DOIUrl":null,"url":null,"abstract":"<p><p>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 <i>in viv</i>o. 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.</p>","PeriodicalId":14512,"journal":{"name":"IntraVital","volume":"4 1","pages":"e1055430"},"PeriodicalIF":0.0000,"publicationDate":"2015-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226011/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IntraVital","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/21659087.2015.1055430","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2015/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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.