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Analysed cap mesenchyme track data from live imaging of mouse kidney development. | LitMetric

Analysed cap mesenchyme track data from live imaging of mouse kidney development.

Data Brief

Division of Genomics of Development and Disease, Institute for Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia; Division of Cell Biology and Molecular Medicine, Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.

Published: December 2016

AI Article Synopsis

Article Abstract

This article provides detailed information on manually tracked cap mesenchyme cells from timelapse imaging of multiple ex vivo embryonic mouse kidneys. Cells were imaged for up to 18 h at 15 or 20 min intervals, and multiple cell divisions were tracked. Positional data is supplemented with a range of information including the relative location of the closest ureteric tip and a correction for drift due to bulk movement and tip growth. A subset of tracks were annotated to indicate the presence of processes attached to the ureteric epithelium. The calculations used for drift correction are described, as are the main methods used in the analysis of this data for the purpose of describing cap cell motility. The outcomes of this analysis are discussed in "Cap mesenchyme cell swarming during kidney development is influenced by attraction, repulsion, and adhesion to the ureteric tip" (A.N. Combes, J.G. Lefevre, S. Wilson, N.A. Hamilton, M.H. Little, 2016) [1].

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018081PMC
http://dx.doi.org/10.1016/j.dib.2016.08.053DOI Listing

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