A computerized cellular imaging system for high content analysis in Monastrol suppressor screens

In this paper, we describe a new bioimage informatics system developed for high content screening (HCS) applications with the goal to extract and analyze phenotypic features of hundreds of thousands of mitotic cells simultaneously. The system introduces the algorithm of multi-phenotypic mitotic analysis (MMA) and integrates that with algorithms of correlation analysis and compound clustering used in gene microarray studies. The HCS-MMA system combines different phenotypic information of cellular images obtained from three-channel acquisitions to distinguish and label individual cells at various phases of mitosis. The proposed system can also be used to extract and count the number of cells in each phase in cell-based assay experiments and archive the extracted data into a structured database for more sophisticated statistical and data analysis. To recognize different mitotic phases, binary patterns are set up based on a known biological mitotic spindle model to characterize cellular morphology of actin, microtubules, and DNA. To illustrate its utility, the HCS-MMA system has been applied to screen the quantitative response of 320 different drug compounds in suppressing Monastrol. The results are validated and evaluated by comparing the performance of HCS-MMA with visual analysis, as well as clustering of the drug compounds under evaluation.

[1]  M V Boland,et al.  Automated recognition of patterns characteristic of subcellular structures in fluorescence microscopy images. , 1998, Cytometry.

[2]  M. Banks,et al.  An ultra-HTS process for the identification of small molecule modulators of orphan G-protein-coupled receptors. , 2003, Drug discovery today.

[3]  Robert F. Murphy,et al.  A neural network classifier capable of recognizing the patterns of all major subcellular structures in fluorescence microscope images of HeLa cells , 2001, Bioinform..

[4]  Robert M. Haralick,et al.  Textural Features for Image Classification , 1973, IEEE Trans. Syst. Man Cybern..

[5]  Timothy J Mitchison,et al.  Dissecting Temporal and Spatial Control of Cytokinesis with a Myosin II Inhibitor , 2003, Science.

[6]  Timothy J. Mitchison,et al.  Eg5 is static in bipolar spindles relative to tubulin , 2001, The Journal of cell biology.

[7]  A. Coulson,et al.  A functional genomic analysis of cell morphology using RNA interference , 2003, Journal of biology.

[8]  Timothy J. Mitchison,et al.  Direct observation of microtubule dynamics at kinetochores in Xenopus extract spindles , 2003, The Journal of cell biology.

[9]  Xiaobo Zhou,et al.  Missing-value estimation using linear and non-linear regression with Bayesian gene selection , 2003, Bioinform..

[10]  M V Boland,et al.  Automated analysis of patterns in fluorescence-microscope images. , 1999, Trends in cell biology.

[11]  T. Mitchison,et al.  Towards a pharmacological genetics. , 1994, Chemistry & biology.

[12]  Makoto Kinoshita,et al.  [Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen]. , 2007, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

[13]  Ashutosh P Jadhav,et al.  Exo1: A new chemical inhibitor of the exocytic pathway , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[14]  N. Perrimon,et al.  Genome-Wide RNAi Analysis of Growth and Viability in Drosophila Cells , 2004, Science.

[15]  Russ B. Altman,et al.  Missing value estimation methods for DNA microarrays , 2001, Bioinform..

[16]  T. Mitchison,et al.  Phenotypic screening of small molecule libraries by high throughput cell imaging. , 2003, Combinatorial chemistry & high throughput screening.

[17]  Lani F. Wu,et al.  Multidimensional Drug Profiling By Automated Microscopy , 2004, Science.

[18]  M. Heck,et al.  Dr. Dolittle and the making of the mitotic spindle. , 1999, BioEssays : news and reviews in molecular, cellular and developmental biology.

[19]  F. Gaunitz,et al.  HTS compatible assay for antioxidative agents using primary cultured hepatocytes. , 2003, Assay and drug development technologies.

[20]  V. Klyushnichenko Protein crystallization: from HTS to kilogram-scale. , 2003, Current opinion in drug discovery & development.

[21]  Mimi Shirasu-Hiza,et al.  Dynamics of the mitotic spindle--potential therapeutic targets. , 2003, Progress in cell cycle research.

[22]  Timothy J Mitchison,et al.  An inner centromere protein that stimulates the microtubule depolymerizing activity of a KinI kinesin. , 2003, Developmental cell.

[23]  Anil K. Jain Fundamentals of Digital Image Processing , 2018, Control of Color Imaging Systems.

[24]  Xiaobo Zhou,et al.  Gene Clustering Based on Clusterwide Mutual Information , 2004, J. Comput. Biol..

[25]  E. Passarge,et al.  Color atlas of genetics , 1995 .

[26]  J. Weitzman,et al.  RNAi and the shape of things to come , 2003, Journal of biology.

[27]  T. Mitchison,et al.  Mitosis: a history of division , 2001, Nature Cell Biology.