| Literature DB >> 31020634 |
Lucía Paniagua-Herranz1,2,3, Rosa Gómez-Villafuertes1,2,3, David de Agustín-Durán1,2,3, Sergio Gascón2,4, Raquel Pérez-Sen1,2,3, Esmerilda G Delicado1,2,3, María Teresa Miras-Portugal1,2,3, Felipe Ortega5,6,7.
Abstract
A comprehensive understanding of the mechanisms controlling the behavior of cell populations with regenerative potential is the first step to design effective therapeutic strategies for many diseases. However, a precise description of the biological events involved, such as proliferation, differentiation, cell fate decisions, migration, or viability, may be hampered by the classical use of experiments based on end-point analysis. By contrast, live imaging and single cell tracking provides researchers with an accurate readout of these features in cells throughout an experiment. Here, we describe a protocol to apply time-lapse video microscopy and post-processing of the data to study critical aspects of the biology and the lineage progression of multiple neural populations.Keywords: Lineage progression; Lineage tree; Live imaging; Neural cells; Single cell tracking; Time-lapse video microscopy
Mesh:
Year: 2020 PMID: 31020634 DOI: 10.1007/7651_2019_219
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745