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Zandstra, P.

Publications and source records attributed to Zandstra, P..

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Context-explorer: Analysis of spatially organized protein expression in high-throughput screens

A growing body of evidence highlights the importance of the cellular microenvironment as a regulator of phenotypic and functional cellular responses to perturbations. We have previously developed cell patterning techniques to control population context parameters, and here we demonstrate Context-explorer (CE), a software tool to improve investigation of microenvironmental variables through colony level analyses. We demonstrate the capabilities of CE in the analysis of human and mouse pluripotent stem cells (hPSCs, mPSCs) patterned in colonies of defined size and shape in multi-well plates.\n\nCE employs a density-based clustering algorithm to identify cell colonies within micropatterned wells. Using this automatic colony classification methodology, we obtain accuracies comparable to manual colony counts in a fraction of the time. Classifying cells according to their relative position within a colony enables statistical analysis of radial spatial trends in protein expression within multiple colonies in the same treatment group. When applied to colonies of hPSCs, our analysis reveals a radial gradient in the expression of the pluripotency inducing transcription factors SOX2 and OCT4, and a similar trend in the intra-colony location of different cellular phenotypes. We extend these analyses to colonies of different sizes and shapes and demonstrate how the metrics derived by CE can be used to asses the patterning fidelity of micropatterned plates.\n\nWe have incorporated a number of features to enhance the usability and utility of CE. To appeal to a broad scientific community, all of the softwares functionality is accessible from a graphical user interface, and convenience functions for several common data operations are included. CE is compatible with existing image analysis programs such as CellProfiler and extends the analytical capabilities already provided by these tools. Taken together, CE facilitates investigation of spatially heterogeneous cell populations in fundamental research and drug development validation programs.

cell biology

Identifying the genetic basis of variation in cell behaviour in human iPS cell lines from healthy donors

Large cohorts of human iPSCs from healthy donors are potentially a powerful tool for investigating the relationship between genetic variants and cellular phenotypes. Here we integrate high content imaging, gene expression and DNA sequence datasets for over 100 human iPSC lines to identify the genetic basis of inter-individual variability in cell behaviour. By applying a dimensionality reduction approach, Probabilistic Estimation of Expression Residuals (PEER), we identified genes that correlated in expression with intrinsic (genetic) and extrinsic (ECM) factors. However, variation in mRNA levels could not account for outlier cell behaviour. Instead, we identified rare, deleterious SNVs in the coding sequence of genes involved in ECM adhesion that occurred in cell lines that were outliers for one or more phenotypes such as cell spreading. These also correlated with altered germ layer differentiation on micropatterned surfaces. Our study thus establishes a strategy for integrating genetic and cell biological measurements for high-throughput analysis.

cell biology