FGF4 Independent Derivation of Trophoblast Stem Cells from the Common Vole
Author(s) -
Е. В. Григорьева,
Alexander I. Shevchenko,
N. A. Mazurok,
Eugeny A. Elisaphenko,
Antonina I. Zhelezova,
Alexander G. Shilov,
П. А. Дыбан,
A. P. Dyban,
Ekaterina M. iashvili,
Sergey Ya. Slobodyanyuk,
Tatyana B. Nesterova,
Neil Brockdorff,
Suren M. Zakian
Publication year - 2009
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0007161
Subject(s) - trophoblast , biology , embryonic stem cell , genomic imprinting , microbiology and biotechnology , multipotent stem cell , stem cell , inner cell mass , cellular differentiation , embryo , genetics , blastocyst , gene , embryogenesis , placenta , gene expression , dna methylation , progenitor cell , fetus , pregnancy
The derivation of stable multipotent trophoblast stem (TS) cell lines from preimplantation, and early postimplantation mouse embryos has been reported previously. FGF4, and its receptor FGFR2, have been identified as embryonic signaling factors responsible for the maintenance of the undifferentiated state of multipotent TS cells. Here we report the derivation of stable TS-like cell lines from the vole M. rossiaemeridionalis , in the absence of FGF4 and heparin. Vole TS-like cells are similar to murine TS cells with respect to their morphology, transcription factor gene expression and differentiation in vitro into derivatives of the trophectoderm lineage, and with respect to their ability to invade and erode host tissues, forming haemorrhagic tumours after subcutaneous injection into nude mice. Moreover, vole TS-like cells carry an inactive paternal X chromosome, indicating that they have undergone imprinted X inactivation, which is characteristic of the trophoblast lineage. Our results indicate that an alternative signaling pathway may be responsible for the establishment and stable proliferation of vole TS-like cells.
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