Journal Article

Live-seq enables temporal transcriptomic recording of single cells

Saelens, Wouter, Klaeger, Amanda, Rainer, Pernille Yde, Dainese, Riccardo, Zachara, Magda, Chen, Wanze, Gäbelein, Christoph G., Zambelli, Tomaso, Deplancke, Bart, Gardeux, Vincent, Vorholt, Julia A., Guillaume-Gentil, Orane

2022

Overview

Single-cell transcriptomics (scRNA-seq) has greatly advanced our ability to characterize cellular heterogeneity 1 . However, scRNA-seq requires lysing cells, which impedes further molecular or functional analyses on the same cells. Here, we established Live-seq, a single-cell transcriptome profiling approach that preserves cell viability during RNA extraction using fluidic force microscopy 2 , 3 , thus allowing to couple a cell’s ground-state transcriptome to its downstream molecular or phenotypic behaviour. To benchmark Live-seq, we used cell growth, functional responses and whole-cell transcriptome read-outs to demonstrate that Live-seq can accurately stratify diverse cell types and states without inducing major cellular perturbations. As a proof of concept, we show that Live-seq can be used to directly map a cell’s trajectory by sequentially profiling the transcriptomes of individual macrophages before and after lipopolysaccharide (LPS) stimulation, and of adipose stromal cells pre- and post-differentiation. In addition, we demonstrate that Live-seq can function as a transcriptomic recorder by preregistering the transcriptomes of individual macrophages that were subsequently monitored by time-lapse imaging after LPS exposure. This enabled the unsupervised, genome-wide ranking of genes on the basis of their ability to affect macrophage LPS response heterogeneity, revealing basal Nfkbia expression level and cell cycle state as important phenotypic determinants, which we experimentally validated. Thus, Live-seq can address a broad range of biological questions by transforming scRNA-seq from an end-point to a temporal analysis approach. Live-seq, a single-cell transcriptome profiling approach that preserves cell viability during RNA extraction using fluidic force microscopy, can address a range of biological questions by transforming scRNA-seq from an end-point to a temporal analysis approach.

• Publisher: Nature Publishing Group UK
• Subject: 38/39 / 631/1647/2017 / 631/208/191/2018 / 631/337/2019 / 631/61/350/1056 / Adipose Tissue - cytology / Cell Cycle - drug effects / Cell Cycle - genetics / Cell Differentiation / Cell Survival / Gene Expression Profiling - methods / Gene Expression Profiling - standards / Genome - drug effects / Genome - genetics / Humanities and Social Sciences / Lipopolysaccharides - immunology / Lipopolysaccharides - pharmacology / Macrophages - cytology / Macrophages - drug effects / Macrophages - immunology / Macrophages - metabolism / multidisciplinary / NF-KappaB Inhibitor alpha - genetics / Organ Specificity / Phenotype / Reproducibility of Results / RNA - genetics / RNA - isolation & purification / RNA-Seq - methods / RNA-Seq - standards / Science / Science (multidisciplinary) / Sequence Analysis, RNA - methods / Sequence Analysis, RNA - standards / Single-Cell Analysis - methods / Stromal Cells - cytology / Stromal Cells - metabolism / Time Factors / Transcriptome - genetics