Accumulation of instability in serial differentiation and reprogramming of parthenogenetic human cells.

ABSTRACT: Human leukocyte antigen-homozygous parthenogenetic stem cells (pSC) could provide a source of progenitors for regenerative medicine, lowering the need for immune suppression in patients. However, the high level of homozygosis and the lack of a paternal genome might pose a safety challenge for their therapeutic use, and no study so far has evaluated the spread and significance of gene expression changes across serial potency changes in these cells. We performed serial rounds of differentiation and reprogramming to assess pSC gene expression stability, likely of epigenetic source. We first derived pSC from activated MII oocytes, and differentiated them to parthenogenetic mesenchymal stem cells (pMSC). We then proceeded to induce pluripotency in pMSC by over expression of the four transcripti

SUBMITTER: Vassena R 

PROVIDER: S-EPMC3491960 | biostudies-literature | 2012 Aug

REPOSITORIES: biostudies-literature