| Literature DB >> 29985644 |
Nguyen P T Huynh1,2,3,4, Bo Zhang3, Farshid Guilak1,2,3.
Abstract
Mesenchymal stem/stromal cells (MSCs) provide an attractive cell source for cartilage repair and cell therapy; however, the underlying molecular pathways that drive chondrogenesis of these populations of adult stem cells remain poorly understood. We generated a rich data set of high-throughput RNA sequencing of human MSCs throughout chondrogenesis at 6 different time points. Our data consisted of 18 libraries with 3 individual donors as biologic replicates, with each library possessing a sequencing depth of 100 million reads. Computational analyses with differential gene expression, gene ontology, and weighted gene correlation network analysis identified dynamic changes in multiple biologic pathways and, most importantly, a chondrogenic gene subset, whose functional characterization promises to further harness the potential of MSCs for cartilage tissue engineering. Furthermore, we created a graphic user interface encyclopedia built with the goal of producing an open resource of transcriptomic regulation for additional data mining and pathway analysis of the process of MSC chondrogenesis.-Huynh, N. P. T., Zhang, B., Guilak, F. High-depth transcriptomic profiling reveals the temporal gene signature of human mesenchymal stem cells during chondrogenesis.Entities:
Keywords: RNA-Seq; chondrocyte; lncRNA; miRNA; pericyte
Mesh:
Year: 2018 PMID: 29985644 PMCID: PMC6355072 DOI: 10.1096/fj.201800534R
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191