Literature DB >> 29177765

XEN and the Art of Stem Cell Maintenance: Molecular Mechanisms Maintaining Cell Fate and Self-Renewal in Extraembryonic Endoderm Stem (XEN) Cell Lines.

Amy Ralston1,2.   

Abstract

The extraembryonic endoderm is one of the first cell types specified during mammalian development. This extraembryonic lineage is known to play multiple important roles throughout mammalian development, including guiding axial patterning and inducing formation of the first blood cells during embryogenesis. Moreover, recent studies have uncovered striking conservation between mouse and human embryos during the stages when extraembryonic endoderm cells are first specified, in terms of both gene expression and morphology. Therefore, mouse embryos serve as an excellent model for understanding the pathways that maintain extraembryonic endoderm cell fate. In addition, self-renewing multipotent stem cell lines, called XEN cells, have been derived from the extraembryonic endoderm of mouse embryos. Mouse XEN cell lines provide an additional tool for understanding the basic mechanisms that contribute to maintaining lineage potential, a resource for identifying how extraembryonic ectoderm specifies fetal cell types, and serve as a paradigm for efforts to establish human equivalents. Given the potential conservation of essential extraembryonic endoderm roles, human XEN cells would provide a considerable advance. However, XEN cell lines have not yet been successfully derived from human embryos. Given the potential utility of human XEN cell lines, this chapter focuses on reviewing the mechanisms known to govern the stem cell properties of mouse XEN, in hopes of facilitating new ways to establish human XEN cell lines.

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Year:  2018        PMID: 29177765     DOI: 10.1007/978-3-319-63187-5_6

Source DB:  PubMed          Journal:  Adv Anat Embryol Cell Biol        ISSN: 0301-5556            Impact factor:   1.231


  2 in total

Review 1.  Opening the black box: Stem cell-based modeling of human post-implantation development.

Authors:  Kenichiro Taniguchi; Idse Heemskerk; Deborah L Gumucio
Journal:  J Cell Biol       Date:  2018-12-14       Impact factor: 10.539

2.  The fetal lineage is susceptible to Zika virus infection within days of fertilization.

Authors:  Jennifer L Watts; Amy Ralston
Journal:  Development       Date:  2022-07-28       Impact factor: 6.862

  2 in total

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