Opto-magnetic capture of individual cells based on visual phenotypes
Loïc Binan,
François Bélanger,
Maxime Uriarte,
Jean François Lemay,
Jean Christophe Pelletier De Koninck,
Joannie Roy,
El Bachir Affar,
Elliot Drobetsky,
Hugo Wurtele,
Santiago Costantino
Affiliations
Loïc Binan
Research Center, Maisonneuve-Rosemont Hospital, Montreal, Canada; Department of Ophthalmology, University of Montreal, Montreal, Canada
François Bélanger
Research Center, Maisonneuve-Rosemont Hospital, Montreal, Canada; Department of Medicine and Molecular Biology Program, University of Montreal, Montreal, Canada
Maxime Uriarte
Research Center, Maisonneuve-Rosemont Hospital, Montreal, Canada; Department of Medicine and Molecular Biology Program, University of Montreal, Montreal, Canada
Research Center, Maisonneuve-Rosemont Hospital, Montreal, Canada
Jean Christophe Pelletier De Koninck
Research Center, Maisonneuve-Rosemont Hospital, Montreal, Canada
Joannie Roy
Research Center, Maisonneuve-Rosemont Hospital, Montreal, Canada
El Bachir Affar
Research Center, Maisonneuve-Rosemont Hospital, Montreal, Canada; Department of Medicine and Molecular Biology Program, University of Montreal, Montreal, Canada
Elliot Drobetsky
Research Center, Maisonneuve-Rosemont Hospital, Montreal, Canada; Department of Medicine and Molecular Biology Program, University of Montreal, Montreal, Canada
Hugo Wurtele
Research Center, Maisonneuve-Rosemont Hospital, Montreal, Canada
The ability to isolate rare live cells within a heterogeneous population based solely on visual criteria remains technically challenging, due largely to limitations imposed by existing sorting technologies. Here, we present a new method that permits labeling cells of interest by attaching streptavidin-coated magnetic beads to their membranes using the lasers of a confocal microscope. A simple magnet allows highly specific isolation of the labeled cells, which then remain viable and proliferate normally. As proof of principle, we tagged, isolated, and expanded individual cells based on three biologically relevant visual characteristics: i) presence of multiple nuclei, ii) accumulation of lipid vesicles, and iii) ability to resolve ionizing radiation-induced DNA damage foci. Our method constitutes a rapid, efficient, and cost-effective approach for isolation and subsequent characterization of rare cells based on observable traits such as movement, shape, or location, which in turn can generate novel mechanistic insights into important biological processes.