PT - JOURNAL ARTICLE AU - Xiongtao Ruan AU - Gregory R. Johnson AU - Iris Bierschenk AU - Roland Nitschke AU - Melanie Boerries AU - Hauke Busch AU - Robert F. Murphy TI - Image-derived Models of Cell Organization Changes During Differentiation of PC12 Cells AID - 10.1101/522763 DP - 2019 Jan 01 TA - bioRxiv PG - 522763 4099 - http://biorxiv.org/content/early/2019/01/16/522763.short 4100 - http://biorxiv.org/content/early/2019/01/16/522763.full AB - Cellular differentiation is a complex process requiring the coordination of many cellular components. PC12 cells are a popular model system to study changes driving and accompanying neuronal differentiation. While significant attention has been paid to changes in transcriptional regulation and protein signaling, much less is known about the changes in cell organization that accompany PC12 differentiation. Fluorescence microscopy can provide extensive information about this, although photobleaching and phototoxicity frequently limit the ability to continuously observe changes in single cells over the many days that differentiation occurs. Here we describe a generative model of differentiation-associated changes in cell and nuclear shape and their relationship to mitochondrial distribution constructed from images of different cells at discrete time points. We show that our spherical harmonic-based model can accurately represent cell and nuclear shapes by measuring reconstruction errors. We then learn a regression model that relates cell and nuclear shape and mitochondrial distribution and observe that the predictive accuracy generally increases during differentiation. Most importantly, we propose a method, based on cell matching and linear interpolation in the shape space, to model the dynamics of cell differentiation using only static images. Without any prior knowledge, the method produces a realistic shape evolution process.Author SummaryCellular differentiation is an important process that is challenging to study due to the number of organizational changes it includes and the different time scales over which it occurs. Fluorescent microscopy is widely used to study cell dynamics and differentiation, but photobleaching and phototoxicity often make it infeasible to continuously observe a single cell undergoing differentiation for several days. In this work, we described a method to model aspects of the dynamics of PC12 cell differentiation without continuous imaging. We constructed accurate representations of cell and nuclear shapes and quantified the relationships between shapes and mitochondrial distributions. We used these to construct a generative model and combined it with a matching process to infer likely sequences of the changes in single cells undergoing differentiation.