Seven-colour multiplex immunochemistry/immunofluorescence and whole slide imaging of frozen sections

多路复用 冰冻切片程序 免疫荧光 病理 免疫化学 背景(考古学) 间质细胞 抗体 医学 生物 免疫学 生物信息学 古生物学
作者
Saem Mul Park,Chun‐Jen J. Chen,Joanna E. Mathy,Shelly C.Y. Lin,Richard C. Martin,Jon A. Mathy,James H. Shaw,P. Rod Dunbar
出处
期刊:Journal of Immunological Methods [Elsevier BV]
卷期号:518: 113490-113490
标识
DOI:10.1016/j.jim.2023.113490
摘要

Multiplex Immunochemistry/Immunofluorescence (mIHC/IF) aims to visualise multiple biomarkers in a single tissue section and is especially powerful when used on slide scanners coupled with digital analysis tools. mIHC/IF is commonly employed in immuno-oncology to characterise features of the tumour microenvironment (TME) and correlate them with clinical parameters to guide prognostication and therapy. However, mIHC/IF can be applied to a wide range of organisms in any physiological or disease context. Recent innovation has extended the number of markers that can be detected using slide scanners well beyond the 3-4 markers typically reported in traditional fluorescence microscopy. However, these methods often require sequential antibody staining and stripping, and are not compatible with frozen tissue sections. Using fluorophore-conjugated antibodies, we have established a simple mIHC/IF imaging workflow that enables simultaneous staining and detection of seven markers in a single section of frozen tissue. Coupled with automated whole slide imaging and digital quantification, our data efficiently revealed the tumour-immune complexity in metastatic melanoma. Computational image analysis quantified the immune and stromal cell populations present in the TME as well as their spatial interactions. This imaging workflow can also be performed with an indirect labelling panel consisting of primary and secondary antibodies. Our new methods, combined with digital quantification, will provide a valuable tool for high-quality mIHC/IF assays in immuno-oncology research and other translational studies, especially in circumstances where frozen sections are required for detection of particular markers, or for applications where frozen sections may be preferred, such as spatial transcriptomics.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
SciGPT应助六六采纳,获得10
刚刚
xty发布了新的文献求助10
1秒前
故香完成签到,获得积分10
1秒前
科研通AI6.1应助我爱科研采纳,获得10
2秒前
2秒前
2秒前
lash应助wulala采纳,获得10
3秒前
Dominos完成签到,获得积分10
3秒前
LEE完成签到 ,获得积分10
3秒前
Orange应助fang采纳,获得10
3秒前
3秒前
呃呃发布了新的文献求助10
3秒前
沁秋发布了新的文献求助10
3秒前
咔嚓发布了新的文献求助10
4秒前
Dan完成签到,获得积分10
4秒前
Hello应助啊w采纳,获得10
5秒前
酷波er应助csz采纳,获得10
6秒前
李睿嘉发布了新的文献求助10
6秒前
7秒前
7秒前
飞龙在天发布了新的文献求助10
7秒前
7秒前
吃了就会胖完成签到 ,获得积分10
8秒前
Aaroncrow完成签到 ,获得积分10
8秒前
9秒前
10秒前
瘦瘦又妍发布了新的文献求助10
11秒前
害怕的小玉完成签到,获得积分10
11秒前
maozi发布了新的文献求助10
11秒前
aqiu发布了新的文献求助10
11秒前
11秒前
zhaoxuemin完成签到,获得积分10
12秒前
Hhh完成签到,获得积分10
13秒前
clock完成签到 ,获得积分10
13秒前
13秒前
123456789发布了新的文献求助10
13秒前
13秒前
张雪晴完成签到,获得积分10
13秒前
HH完成签到,获得积分10
14秒前
shaaa完成签到,获得积分10
14秒前
高分求助中
Entre Praga y Madrid: los contactos checoslovaco-españoles (1948-1977) 1000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
Hope Teacher Rating Scale 600
Death Without End: Korea and the Thanatographics of War 500
Der Gleislage auf der Spur 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6091245
求助须知:如何正确求助?哪些是违规求助? 7921104
关于积分的说明 16395026
捐赠科研通 5223196
什么是DOI,文献DOI怎么找? 2792153
邀请新用户注册赠送积分活动 1775002
关于科研通互助平台的介绍 1649956