A single-cell translocation and secretion assay (TransSeA). Issue 20 (4th September 2018)

• Record Type: Journal Article
• Authors: Cai, Wei; Chiu, Yu-Jui; Ramakrishnan, Valya; Tsai, Yihuan; Chen, Clark; Lo, Yu-Hwa
• Is Part Of: Lab on a chip. Volume 18:Issue 20(2018)
• Page Start: 3154
• Page End: 3162
• Publication Date: 2018-09-04
• Subjects: Miniature electronic equipment -- Periodicals; Combinatorial chemistry -- Periodicals; Biotechnology -- Periodicals; 543.0813
• DOI: 10.1039/c8lc00821c
• Languages: English
• ISSNs: 1473-0197

Abstract

Abstract : Single cell TransSeA can support the studies of the cargos of single cell secretions, massively parallel translocation and genealogy and hereditary properties of single cells. Abstract : Understanding biological heterogeneity at the single cell level is required for advancing insights into the complexity of human physiology and diseases. While advances in technological and analytical methods have afforded unprecedented glimpses of this heterogeneity, the information captured to date largely represents one-time "snap" shots of single cell physiology. To address the limits of existing methods and to accelerate discoveries from single cell studies, we developed a single-cell translocation and secretion assay (TransSeA) that supports time lapse analysis, enables molecular cargo analysis of secretions such as extracellular vesicles (EVs) from single cells, allows massively parallel single cell transfer according to user-defined cell selection criteria, and supports tracking of phenotypes between parental and progeny cells derived from single cells. To demonstrate the unique capabilities and efficiencies of the assay, we present unprecedented single cell studies related to cell secretions, EV cargos and cell intrinsic properties. Although used as examples to demonstrate the feasibility and versatility of the technology, the studies already provided insights into key unanswered questions such as the microRNAs carried by EVs, the relationships between EV secretion rates and gene expressions, and the spontaneous, trans-generational phenotypic changes in EV secretion between parental and progeny cells.