| Literature DB >> 24516164 |
Sinisa Hrvatin1, Charles W O'Donnell, Francis Deng, Jeffrey R Millman, Felicia Walton Pagliuca, Philip DiIorio, Alireza Rezania, David K Gifford, Douglas A Melton.
Abstract
Human pluripotent stem cells (hPSCs) have the potential to generate any human cell type, and one widely recognized goal is to make pancreatic β cells. To this end, comparisons between differentiated cell types produced in vitro and their in vivo counterparts are essential to validate hPSC-derived cells. Genome-wide transcriptional analysis of sorted insulin-expressing (INS(+)) cells derived from three independent hPSC lines, human fetal pancreata, and adult human islets points to two major conclusions: (i) Different hPSC lines produce highly similar INS(+) cells and (ii) hPSC-derived INS(+) (hPSC-INS(+)) cells more closely resemble human fetal β cells than adult β cells. This study provides a direct comparison of transcriptional programs between pure hPSC-INS(+) cells and true β cells and provides a catalog of genes whose manipulation may convert hPSC-INS(+) cells into functional β cells.Entities:
Keywords: MARIS; beta cells; differentiation; transcriptional profiling
Mesh:
Year: 2014 PMID: 24516164 PMCID: PMC3939927 DOI: 10.1073/pnas.1400709111
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205