Getting the whole picture: High content screening using three-dimensional cellular model systems and whole animal assays

被引:18
作者
Kriston-Vizi, Janos [1 ]
Flotow, Horst [2 ]
机构
[1] UCL, MRC Lab Mol Cell Biol, Bioinformat Image Core, London, England
[2] HDC GmbH, Byk Gulden Str 2, Constance, Germany
基金
英国医学研究理事会;
关键词
high content screening; 3D tissue culture; automated image analysis; phenotypic assays; HIGH-THROUGHPUT; DRUG DISCOVERY; IMAGE DATA; CULTURE; SPHEROIDS; CELLS; MORPHOGENESIS; VISUALIZATION; ONCOGENESIS; MICROSCOPY;
D O I
10.1002/cyto.a.22907
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Phenotypic or High Content Screening (HCS) is becoming more widely used for primary screening campaigns in drug discovery. Currently the vast majority of HCS campaigns are using cell lines grown in well-established monolayer cultures (2D tissue culture). There is widespread recognition that the more biologically relevant 3D tissue culture technologies such as spheroids and organoids and even whole animal assays will eventually be run as primary HCS. Upgrading the IT infrastructure to cope with the increase in data volumes requires investments in hardware (and software) and this will be manageable. However, the main bottleneck for the effective adoption and use of 3D tissue culture and whole animal assays in HCS is anticipated to be the development of software for the analysis of 3D images. In this review we summarize the current state of the available software and how they may be applied to analyzing 3D images obtained from a HCS campaign. (c) 2016 International Society for Advancement of Cytometry
引用
收藏
页码:152 / 159
页数:8
相关论文
共 76 条
[1]  
Abrmoff MD., 2004, Image Processing with ImageJ, V11, P36, DOI DOI 10.1201/9781420005615.AX4
[2]  
[Anonymous], 1982, Digital Picture Processing. Computer Science and Applied Mathematics
[3]  
Bernsen J., 1986, DYNAMIC THRESHOLDING, P1251
[4]   Statistical methods for analysis of high-throughput RNA interference screens [J].
Birmingham, Amanda ;
Selfors, Laura M. ;
Forster, Thorsten ;
Wrobel, David ;
Kennedy, Caleb J. ;
Shanks, Emma ;
Santoyo-Lopez, Javier ;
Dunican, Dara J. ;
Long, Aideen ;
Kelleher, Dermot ;
Smith, Queta ;
Beijersbergen, Roderick L. ;
Ghazal, Peter ;
Shamu, Caroline E. .
NATURE METHODS, 2009, 6 (08) :569-575
[5]   A guided tour into subcellular colocalization analysis in light microscopy [J].
Bolte, S. ;
Cordelieres, F. P. .
JOURNAL OF MICROSCOPY, 2006, 224 (213-232) :213-232
[6]   On digital distance transforms in three dimensions [J].
Borgefors, G .
COMPUTER VISION AND IMAGE UNDERSTANDING, 1996, 64 (03) :368-376
[7]   The art and design of genetic screens: RNA interference [J].
Boutros, Michael ;
Ahringer, Julie .
NATURE REVIEWS GENETICS, 2008, 9 (07) :554-566
[8]   Analysis of cell-based RNAi screens [J].
Boutros, Michael ;
Bras, Ligia P. ;
Huber, Wolfgang .
GENOME BIOLOGY, 2006, 7 (07)
[9]   Medical progress - Ductal carcinoma in situ of the breast [J].
Burstein, HJ ;
Polyak, K ;
Wong, JS ;
Lester, SC ;
Kaelin, CM .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (14) :1430-1441
[10]   A practical guide to hydrogels for cell culture [J].
Caliari, Steven R. ;
Burdick, Jason A. .
NATURE METHODS, 2016, 13 (05) :405-414