Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015;14(3):85-98.
doi: 10.1007/s12522-014-0199-8. Epub 2014 Dec 3.

How are pluripotent cells captured in culture?

Affiliations

How are pluripotent cells captured in culture?

Masaki Kinoshita. Reprod Med Biol. 2015.

Abstract

In mice, three pluripotent stem cell lines have been established from different stage of developing embryo, which are embryonic stem (ES) cell, post-implantation epiblast stem cell (EpiSC), and embryonic germ (EG) cell. ES cell and EG cell share many common features including factor requirement, colony morphology, and gene expression pattern. On the other hand, EpiSC needs different external signal inputs, exhibits flattened colony morphology, and a different set of gene expression patterns. In addition, the germ line competency of EpiSCs is still unclear. To distinguish the differences between them, they are defined by the words "naïve" and "primed" pluripotent cells, respectively. This article introduces how pluripotent stem cell lines are established in culture, and how much those cells in vitro are similar or relevant to their in vivo origin and the knowledge about transcription factors to support this state.

Keywords: EG cells; ES cell; EpiSC; Epiblast; Pluripotency.

PubMed Disclaimer

Conflict of interest statement

Masaki Kinoshita declares that he has no conflicts of interest to disclose.

Figures

Figure 1
Figure 1
Pluripotent cells in culture and their origin in embryos a E4.5 mouse embryo. a’ Mouse embryonic stem cell cultured in 2i and LIF on a gelatin‐coated plate. b E5.5 mouse embryo. b’ Mouse EpiSC cultured in activin and bFGF on fibronectin‐coated plate. c E8.5 mouse embryo. c’ Mouse EG cells cultured in 2i and LIF with feeder cells. Cells in blue in (a, b) show the pluripotent epiblast and in c show the location of PGC cells at this stage. Red cells in (a, b) are extra‐embryonic endoderm cells. Scale bar in a, b is 50 µm and a’c’ is 100 µm

Similar articles

Cited by

References

    1. Yamanaka Y, Lanner F, Rossant J. FGF signal‐dependent segregation of primitive endoderm and epiblast in the mouse blastocyst. Development, 2010, 137, 715–724 - PubMed
    1. Nishioka N, Inoue K, Adachi K, Kiyonari H, Ota M, Ralston A et al. The Hippo signaling pathway components Lats and Yap pattern Tead4 activity to distinguish mouse trophectoderm from inner cell mass. Dev Cell, 2009, 16, 398–410 - PubMed
    1. Chazaud C, Yamanaka Y, Pawson T, Rossant J. Early lineage segregation between epiblast and primitive endoderm in mouse blastocysts through the Grb2‐MAPK pathway. Dev Cell, 2006, 10, 615–624 - PubMed
    1. Plusa B, Piliszek A, Frankenberg S, Artus J, Hadjantonakis AK. Distinct sequential cell behaviours direct primitive endoderm formation in the mouse blastocyst. Development, 2008, 135, 3081–30912768606 - PMC - PubMed
    1. Meilhac SM, Adams RJ, Morris SA, Danckaert A, Garrec JF, Zernicka‐Goetz M. Active cell movements coupled to positional induction are involved in lineage segregation in the mouse blastocyst. Dev Biol, 2009, 331, 210–2213353123 - PMC - PubMed

LinkOut - more resources