Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2105-12-S13-S19
Title: Correlation of cell membrane dynamics and cell motility
Authors: Veronika, M.
Welsch, R.
Ng, A.
Matsudaira, P. 
Rajapakse, J.C.
Issue Date: 30-Nov-2011
Citation: Veronika, M., Welsch, R., Ng, A., Matsudaira, P., Rajapakse, J.C. (2011-11-30). Correlation of cell membrane dynamics and cell motility. BMC Bioinformatics 12 (SUPPL. 13) : -. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2105-12-S13-S19
Abstract: Background: Essential events of cell development and homeostasis are revealed by the associated changes of cell morphology and therefore have been widely used as a key indicator of physiological states and molecular pathways affecting various cellular functions via cytoskeleton. Cell motility is a complex phenomenon primarily driven by the actin network, which plays an important role in shaping the morphology of the cells. Most of the morphology based features are approximated from cell periphery but its dynamics have received none to scant attention. We aim to bridge the gap between membrane dynamics and cell states from the perspective of whole cell movement by identifying cell edge patterns and its correlation with cell dynamics.Results: We present a systematic study to extract, classify, and compare cell dynamics in terms of cell motility and edge activity. Cell motility features extracted by fitting a persistent random walk were used to identify the initial set of cell subpopulations. We propose algorithms to extract edge features along the entire cell periphery such as protrusion and retraction velocity. These constitute a unique set of multivariate time-lapse edge features that are then used to profile subclasses of cell dynamics by unsupervised clustering.Conclusions: By comparing membrane dynamic patterns exhibited by each subclass of cells, correlated trends of edge and cell movements were identified. Our findings are consistent with published literature and we also identified that motility patterns are influenced by edge features from initial time points compared to later sampling intervals. © 2011 Veronika et al; licensee BioMed Central Ltd.
Source Title: BMC Bioinformatics
URI: http://scholarbank.nus.edu.sg/handle/10635/114308
ISSN: 14712105
DOI: 10.1186/1471-2105-12-S13-S19
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