Martin Lee, Andy Downes, You-Ying Chau, Bryan Serrels, Nick Hastie, Alistair Elfick, Valerie Brunton, Margaret Frame, Alan Serrels
{"title":"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。","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":"{\"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}","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}
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.