Feiyang Ma1, Gloria E Hernandez1, Milagros Romay2, M Luisa Iruela-Arispe2. 1. Molecular Biology Institute, University of California, Los Angeles, California. 2. Department of Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Abstract
PURPOSE OF REVIEW: Single-cell RNA sequencing (scRNA-seq) can capture the transcriptional profile of thousands of individual cells concurrently from complex tissues and with remarkable resolution. Either with the goal of seeking information about distinct cell subtypes or responses to a stimulus, the approach has provided robust information and promoted impressive advances in cardiovascular research. The goal of this review is to highlight strategies and approaches to leverage this technology and bypass potential caveats related to evaluation of the vascular cells. RECENT FINDINGS: As the most recent technological development, details associated with experimental strategies, analysis, and interpretation of scRNA-seq data are still being discussed and scrutinized by investigators across the vascular field. Compilation of this information is valuable for those using the technology but particularly important to those about to start utilizing scRNA-seq to seek transcriptome information of vascular cells. SUMMARY: As our field progresses to catalog transcriptomes from distinct vascular beds, it is undeniable that scRNA-seq technology is here to stay. Sharing approaches to improve the quality of cell dissociation procedures, analysis, and a consensus of best practices is critical as information from this powerful experimental platform continues to emerge.
PURPOSE OF REVIEW: Single-cell RNA sequencing (scRNA-seq) can capture the transcriptional profile of thousands of individual cells concurrently from complex tissues and with remarkable resolution. Either with the goal of seeking information about distinct cell subtypes or responses to a stimulus, the approach has provided robust information and promoted impressive advances in cardiovascular research. The goal of this review is to highlight strategies and approaches to leverage this technology and bypass potential caveats related to evaluation of the vascular cells. RECENT FINDINGS: As the most recent technological development, details associated with experimental strategies, analysis, and interpretation of scRNA-seq data are still being discussed and scrutinized by investigators across the vascular field. Compilation of this information is valuable for those using the technology but particularly important to those about to start utilizing scRNA-seq to seek transcriptome information of vascular cells. SUMMARY: As our field progresses to catalog transcriptomes from distinct vascular beds, it is undeniable that scRNA-seq technology is here to stay. Sharing approaches to improve the quality of cell dissociation procedures, analysis, and a consensus of best practices is critical as information from this powerful experimental platform continues to emerge.
Authors: Samuel G Rodriques; Robert R Stickels; Aleksandrina Goeva; Carly A Martin; Evan Murray; Charles R Vanderburg; Joshua Welch; Linlin M Chen; Fei Chen; Evan Z Macosko Journal: Science Date: 2019-03-28 Impact factor: 47.728
Authors: Susanne C van den Brink; Fanny Sage; Ábel Vértesy; Bastiaan Spanjaard; Josi Peterson-Maduro; Chloé S Baron; Catherine Robin; Alexander van Oudenaarden Journal: Nat Methods Date: 2017-09-29 Impact factor: 28.547
Authors: Aaron T L Lun; Samantha Riesenfeld; Tallulah Andrews; The Phuong Dao; Tomas Gomes; John C Marioni Journal: Genome Biol Date: 2019-03-22 Impact factor: 13.583
Authors: Huidong Chen; Caleb Lareau; Tommaso Andreani; Michael E Vinyard; Sara P Garcia; Kendell Clement; Miguel A Andrade-Navarro; Jason D Buenrostro; Luca Pinello Journal: Genome Biol Date: 2019-11-18 Impact factor: 13.583
Authors: Gloria E Hernandez; Feiyang Ma; Guadalupe Martinez; Nadia B Firozabadi; Jocelynda Salvador; Lih Jiin Juang; Jerry Leung; Peng Zhao; Diego A López; Reza Ardehali; Anna E Beaudin; Christian J Kastrup; Matteo Pellegrini; Matthew J Flick; M Luisa Iruela-Arispe Journal: Nat Cardiovasc Res Date: 2022-01-12