Reprogramming mechanisms influence the maturation of hematopoietic progenitors from human pluripotent stem cells. Issue 11 (November 2018)
- Record Type:
- Journal Article
- Title:
- Reprogramming mechanisms influence the maturation of hematopoietic progenitors from human pluripotent stem cells. Issue 11 (November 2018)
- Main Title:
- Reprogramming mechanisms influence the maturation of hematopoietic progenitors from human pluripotent stem cells
- Authors:
- Heo, Hye-Ryeon
Song, Haengseok
Kim, Hye-Ryun
Lee, Jeong
Chung, Young
Kim, Woo
Yang, Se-Ran
Kim, Kye-Seong
Chun, Taehoon
Lee, Dong
Hong, Seok-Ho - Abstract:
- Abstract Somatic cell nuclear transfer (SCNT) or the forced expression of transcription factors can be used to generate autologous pluripotent stem cells (PSCs). Although transcriptomic and epigenomic comparisons of isogenic human NT-embryonic stem cells (NT-ESCs) and induced PSCs (iPSCs) in the undifferentiated state have been reported, their functional similarities and differentiation potentials have not been fully elucidated. Our study showed that NT-ESCs and iPSCs derived from the same donors generally displayed similar in vitro commitment capacity toward three germ layer lineages as well as proliferative activity and clonogenic capacity. However, the maturation capacity of NT-ESC-derived hematopoietic progenitors was significantly greater than the corresponding capacity of isogenic iPSC-derived progenitors. Additionally, donor-dependent variations in hematopoietic specification and commitment capacity were observed. Transcriptome and methylome analyses in undifferentiated NT-ESCs and iPSCs revealed a set of genes that may influence variations in hematopoietic commitment and maturation between PSC lines derived using different reprogramming methods. Here, we suggest that genetically identical iPSCs and NT-ESCs could be functionally unequal due to differential transcription and methylation levels acquired during reprogramming. Our proof-of-concept study indicates that reprogramming mechanisms and genetic background could contribute to diverse functionalities between PSCs.
- Is Part Of:
- Cell death and disease. Volume 9:Issue 11(2018)
- Journal:
- Cell death and disease
- Issue:
- Volume 9:Issue 11(2018)
- Issue Display:
- Volume 9, Issue 11 (2018)
- Year:
- 2018
- Volume:
- 9
- Issue:
- 11
- Issue Sort Value:
- 2018-0009-0011-0000
- Page Start:
- 1
- Page End:
- 13
- Publication Date:
- 2018-11
- Subjects:
- Cell death -- Periodicals
Apoptosis -- Periodicals
571.936 - Journal URLs:
- http://www.nature.com/cddis/index.html ↗
http://www.nature.com/ ↗ - DOI:
- 10.1038/s41419-018-1124-6 ↗
- Languages:
- English
- ISSNs:
- 2041-4889
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.749000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 10577.xml