| Literature DB >> 27863245 |
Vionnie W C Yu1, Rushdia Z Yusuf1, Toshihiko Oki1, Juwell Wu2, Borja Saez1, Xin Wang3, Colleen Cook1, Ninib Baryawno1, Michael J Ziller4, Eunjung Lee5, Hongcang Gu2, Alexander Meissner4, Charles P Lin6, Peter V Kharchenko7, David T Scadden8.
Abstract
Stem cells determine homeostasis and repair of many tissues and are increasingly recognized as functionally heterogeneous. To define the extent of-and molecular basis for-heterogeneity, we overlaid functional, transcriptional, and epigenetic attributes of hematopoietic stem cells (HSCs) at a clonal level using endogenous fluorescent tagging. Endogenous HSC had clone-specific functional attributes over time in vivo. The intra-clonal behaviors were highly stereotypic, conserved under the stress of transplantation, inflammation, and genotoxic injury, and associated with distinctive transcriptional, DNA methylation, and chromatin accessibility patterns. Further, HSC function corresponded to epigenetic configuration but not always to transcriptional state. Therefore, hematopoiesis under homeostatic and stress conditions represents the integrated action of highly heterogeneous clones of HSC with epigenetically scripted behaviors. This high degree of epigenetically driven cell autonomy among HSCs implies that refinement of the concepts of stem cell plasticity and of the stem cell niche is warranted.Entities:
Keywords: ATAC-seq; RNA-seq; clonal tracking; epigenetic memory; hematopoiesis; hematopoietic stem cell; lineage tracing; multi-fluorescent mouse model; single cell; transplantation
Mesh:
Year: 2016 PMID: 27863245 DOI: 10.1016/j.cell.2016.10.045
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582