Single cell RNA-seq identifies the origins of heterogeneity in efficient cell transdifferentiation and reprogramming.
Ontology highlight
ABSTRACT: Forced transcription factor expression can transdifferentiate somatic cells into other specialised cell types or reprogram them into induced pluripotent stem cells (iPSCs) with variable efficiency. To better understand the heterogeneity of these processes, we used single-cell RNA sequencing to follow the transdifferentation of murine pre-B cells into macrophages as well as their reprogramming into iPSCs. Even in these highly efficient systems, there was substantial variation in the speed and path of fate conversion. We predicted and validated that these differences are inversely coupled and arise in the starting cell population, with Mychigh large pre-BII cells transdifferentiating slowly but reprogramming efficiently and Myclow small pre-BII cells transdifferentiatin
SUBMITTER: Francesconi M
PROVIDER: S-EPMC6435319 | biostudies-literature | 2019 Mar
REPOSITORIES: biostudies-literature
ACCESS DATA