| Literature DB >> 35932315 |
Noriko Hiramatsu1,2, Naoki Yamamoto3,4,5,6, Mahito Ohkuma7, Noriaki Nagai8, Ei-Ichi Miyachi7,9, Kumiko Yamatsuta10, Kazuyoshi Imaizumi10.
Abstract
When regenerated tissue is generated from induced pluripotent stem cells (iPSCs), it is necessary to track and identify the transplanted cells. Fluorescently-labeled iPSCs synthesize a fluorescent substance that is easily tracked. However, the expressed protein should not affect the original genome sequence or pluripotency. To solve this problem, we created a cell tool for basic research on iPSCs. Iris tissue-derived cells from GFP fluorescence-expressing mice (GFP-DBA/2 mice) were reprogrammed to generate GFP mouse iris-derived iPSCs (M-iris GFP iPSCs). M-iris GFP iPSCs expressed cell markers characteristic of iPSCs and showed pluripotency in differentiating into the three germ layers. In addition, when expressing GFP, the cells differentiated into functional recoverin- and calbindin-positive cells. Thus, this cell line will facilitate future studies on iPSCs.Entities:
Keywords: Electrophysiology; Green fluorescent protein; Mouse iris-derived induced pluripotent stem cells; Neurons
Year: 2022 PMID: 35932315 DOI: 10.1007/s00795-022-00330-z
Source DB: PubMed Journal: Med Mol Morphol ISSN: 1860-1499 Impact factor: 2.070