A fluorescent chemical probe CDy9 selectively stains and enables the isolation of live naive mouse embryonic stem cells

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Title
A fluorescent chemical probe CDy9 selectively stains and enables the isolation of live naive mouse embryonic stem cells
Author(s)
S J Cho; K T Kim; J S Kim; Ok Seon Kwon; Y H Go; N Y Kang; Haejeong Huh; Mi Rang Kim; D W Han; Sung-Hwan Moon; Y T Chang; H J Cha
Bibliographic Citation
Biomaterials, vol. 180, pp. 12-23
Publication Year
2018
Abstract
Human and mouse embryonic stem cells (ESCs) differ in terms of their pluripotency status, i.e., naive vs. primed. This affects various biological properties and leads to several technical hurdles for future clinical applications, such as difficulties in chimera formation, single-cell passaging, and gene editing. In terms of generating functional human tissues and organs via mammalian interspecies chimerism, a fluorescent chemical probe that specifically labels naive ESCs would help to isolate these cells and monitor their conversion. This study demonstrates that the fluorescent chemical probe compound of designation yellow 9 (CDy9) selectively stains naive, but not primed, mouse ESCs (mESCs). CDy9 entered cells via Slc13a5, a highly expressed membrane transporter in naive mESCs. Fluorescence-based cell sorting based on CDy9 staining successfully separated naive mESCs from primed mESCs. Mice generated using CDy9+ cells isolated during the conversion of mouse epiblast stem cells into naive mESCs exhibited coat color chimerism. Furthermore, CDy9 specifically stained cells in the inner cell mass of mouse embryos. These findings suggest that CDy9 is a useful tool to isolate functional naive mESCs.
Keyword
Fluorescence probeInner cell massLive isolationNaive ESCsPrimed ESCsSlc13a5
ISSN
0142-9612
Publisher
Elsevier
Full Text Link
http://dx.doi.org/10.1016/j.biomaterials.2018.07.007
Type
Article
Appears in Collections:
Division of Research on National Challenges > Stem Cell Convergenece Research Center > 1. Journal Articles
Aging Convergence Research Center > 1. Journal Articles
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