| Literature DB >> 28720304 |
Lixia Zhao1, Zixin Wang2, Jindun Zhang3, Jian Yang4, Xuefei Gao4, Baojiang Wu2, Gaoping Zhao2, Siqin Bao3, Shuxiang Hu1, Pentao Liu4, Xihe Li5.
Abstract
Single-cell derived bovine induced pluripotent stem cells (iPSCs) were generated by the introduction of piggyBac transposons with CAG promoting transcription factors (Oct3/4, Sox2, Klf4 and cMyc). In the study, the bovine iPSCs colony from single cell could passage more than 50 passages after enzymatic dissociation into single cells. These bovine iPSCs cells kept the normal karyotype and displayed dome shaped clones similar to mouse embryonic stem cells. They showed pluripotency in many ways, including their expression of pluripotency markers, such as OCT3/4, NANOG, SOX2, SSEA1, SSEA4, and AP in immunofluorescence assay, Oct4, Nanog, Sox2, Klf4 and cMyc in RT-PCR. Additionally, single-cell derived bovine iPSCs formed embryoid bodies and teratomas that all subsequently gave rise to differentiated cells from all three embryonic germ layers. The results showed that our reprogramming method could obtain high efficiency single-cell cloning bovine iPSCs, and the efficiency of single cell cloning is 40%.Entities:
Keywords: Bovine iPSCs; Pluripotency; Single-cell; piggyBac
Mesh:
Year: 2017 PMID: 28720304 DOI: 10.1016/j.tice.2017.05.005
Source DB: PubMed Journal: Tissue Cell ISSN: 0040-8166 Impact factor: 2.466