| Literature DB >> 29078333 |
Tian-Da Li1, Gui-Hai Feng1, Yu-Fei Li1,2, Mei Wang1,3, Jun-Jie Mao1,2, Jia-Qiang Wang1, Xin Li1, Xue-Peng Wang1,2, Bin Qu1,2, Le-Yun Wang1,4, Xin-Xin Zhang1,4, Hai-Feng Wan1, Tong-Tong Cui1,2, Cong Wan1, Lei Liu1, Xiao-Yang Zhao3, Bao-Yang Hu1, Wei Li1, Qi Zhou5.
Abstract
Pluripotency of embryonic stem cells (ESCs) can be functionally assessed according to the developmental potency. Tetraploid complementation, through which an entire organism is produced from the pluripotent donor cells, is taken as the most stringent test for pluripotency. It remains unclear whether ESCs of other species besides mice can pass this test. Here we show that the rat ESCs derived under 2i (two small molecule inhibitors) conditions at very early passages are able to produce fertile offspring by tetraploid complementation. However, they lose this capacity rapidly during culture due to a nearly complete loss of genomic imprinting. Our findings support that the naïve ground state pluripotency can be captured in rat ESCs but also point to the species-specific differences in its regulation and maintenance, which have implications for the derivation and application of naïve pluripotent stem cells in other species including human. Published under the PNAS license.Entities:
Keywords: embryonic stem cells; imprinted gene; pluripotency; rat; tetraploid complementation
Mesh:
Year: 2017 PMID: 29078333 PMCID: PMC5692557 DOI: 10.1073/pnas.1708710114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205