Extra-embryonic endoderm cells derived from ES cells induced by GATA Factors acquire the character of XEN cells

BackgroundThree types of cell lines have been established from mouse blastocysts: embryonic stem (ES) cells, trophoblast stem (TS) cells, and extra-embryonic endoderm (XEN) cells, which have the potential to differentiate into their respective cognate lineages. ES cells can differentiate in vitro not only into somatic cell lineages but into extra-embryonic lineages, including trophectoderm and extra-embryonic endoderm (ExEn) as well. TS cells can be established from ES cells by the artificial repression of Oct3/4 or the upregulation of Cdx2 in the presence of FGF4 on feeder cells. The relationship between these embryo-derived XEN cells and ES cell-derived ExEn cell lines remains unclear, although we have previously reported that overexpression of Gata4 or Gata6 induces differentiation of mouse ES cells into extra-embryonic endoderm in vitro.ResultsA system in which GATA factors were conditionally activated revealed that the cells continue to proliferate while expressing a set of extra-embryonic endoderm markers, and, following injection into blastocysts, contribute only to the extra-embryonic endoderm lineage in vivo. Although the in vivo contribution is limited to cells of parietal endoderm lineage, Gata-induced extra-embryonic endoderm cells (gExEn) can be induced to differentiate into visceral endoderm-like cells in vitro by repression of Gata6. During early passage, the propagation of gExEn cells is dependent on the expression of the Gata6 transgene. These cells, however, lose this dependency following establishment of endogenous Gata6 expression.ConclusionWe show here that Gata-induced extra-embryonic endoderm cells derived from ES cells mimic the character of XEN cells. These findings indicate that Gata transcription factors are sufficient for the derivation and propagation of XEN-like extra-embryonic endoderm cells from ES cells.

[1]  J. Miyazaki,et al.  Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells , 2000, Nature Genetics.

[2]  U. Wewer Characterization of a rat yolk sac carcinoma cell line. , 1982, Developmental biology.

[3]  W. D. Martin,et al.  Disabled-2 is essential for endodermal cell positioning and structure formation during mouse embryogenesis. , 2002, Developmental biology.

[4]  M. Goumans,et al.  Expression of activin subunits, activin receptors and follistatin in postimplantation mouse embryos suggests specific developmental functions for different activins. , 1994, Development.

[5]  J. Miyazaki,et al.  Phenotypic Complementation Establishes Requirements for Specific POU Domain and Generic Transactivation Function of Oct-3/4 in Embryonic Stem Cells , 2002, Molecular and Cellular Biology.

[6]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[7]  Tony Pawson,et al.  Early lineage segregation between epiblast and primitive endoderm in mouse blastocysts through the Grb2-MAPK pathway. , 2006, Developmental cell.

[8]  S. Becker,et al.  Indian hedgehog signaling in extraembryonic endoderm and ectoderm differentiation in ES embryoid bodies , 2000, Mechanisms of Development.

[9]  J. Fléchon,et al.  Parietal endoderm cell line from a rat blastocyst. , 2001, Placenta.

[10]  E. Adamson,et al.  Localization and synthesis of alphafoetoprotein in post-implantation mouse embryos. , 1978, Journal of embryology and experimental morphology.

[11]  Hitoshi Niwa,et al.  How is pluripotency determined and maintained? , 2007, Development.

[12]  H. Niwa,et al.  An efficient system to establish multiple embryonic stem cell lines carrying an inducible expression unit , 2005, Nucleic acids research.

[13]  Janet Rossant,et al.  Interaction between Oct3/4 and Cdx2 Determines Trophectoderm Differentiation , 2005, Cell.

[14]  B. Hogan,et al.  Incorporation into Reichert's membrane of laminin-like extracellular proteins synthesized by parietal endoderm cells of the mouse embryo. , 1980, Developmental biology.

[15]  E. Morrisey,et al.  Perception of differentiation cues by GATA factors in primitive endoderm lineage determination of mouse embryonic stem cells. , 2005, Developmental biology.

[16]  Yoshiakira Kanai,et al.  Depletion of definitive gut endoderm in Sox17-null mutant mice. , 2002, Development.

[17]  E. Morrisey,et al.  GATA-6: a zinc finger transcription factor that is expressed in multiple cell lineages derived from lateral mesoderm. , 1996, Developmental biology.

[18]  Makoto Kobayashi,et al.  Hematopoietic regulatory domain of gata1 gene is positively regulated by GATA1 protein in zebrafish embryos. , 2001, Development.

[19]  John K. Heath,et al.  Inhibition of pluripotential embryonic stem cell differentiation by purified polypeptides , 1988, Nature.

[20]  J. Casanova,et al.  The role of cell interactions in the differentiation of teratocarcinoma-derived parietal and visceral endoderm. , 1988, Developmental biology.

[21]  K. Sekiguchi,et al.  Sox7 Plays Crucial Roles in Parietal Endoderm Differentiation in F9 Embryonal Carcinoma Cells through Regulating Gata-4 and Gata-6 Expression , 2004, Molecular and Cellular Biology.

[22]  H. Niwa,et al.  Endoderm-specific gene expression in embryonic stem cells differentiated to embryoid bodies. , 1996, Experimental cell research.

[23]  M. Dziadek,et al.  In vitro production of Reichert's membrane by mouse embryo-derived parietal endoderm cell lines. , 1990, Experimental cell research.

[24]  Simon,et al.  Mouse GATA-4: a retinoic acid-inducible GATA-binding transcription factor expressed in endodermally derived tissues and heart , 1993, Molecular and cellular biology.

[25]  E. Morrisey,et al.  GATA6 regulates HNF4 and is required for differentiation of visceral endoderm in the mouse embryo. , 1998, Genes & development.

[26]  K. Mizuseki,et al.  Induction of Midbrain Dopaminergic Neurons from ES Cells by Stromal Cell–Derived Inducing Activity , 2000, Neuron.

[27]  J. Rossant,et al.  Imprinted X-inactivation in extra-embryonic endoderm cell lines from mouse blastocysts , 2005, Development.

[28]  F. Grosveld,et al.  The transcription factor GATA6 is essential for early extraembryonic development. , 1999, Development.

[29]  Kazuwa Nakao,et al.  Differentiation of embryonic stem cells is induced by GATA factors. , 2002, Genes & development.

[30]  B. Lanske,et al.  Parathyroid hormone-related peptide (PTHrP) induces parietal endoderm formation exclusively via the Type I PTH/PTHrP receptor , 1999, Mechanisms of Development.

[31]  D. Belin,et al.  The production of distinct forms of plasminogen activator by mouse embryonic cells. , 1982, Developmental biology.

[32]  C. Dickson,et al.  Retinoic Acid-regulated Expression of Fibroblast Growth Factor 3 Requires the Interaction between a Novel Transcription Factor and GATA-4* , 1999, The Journal of Biological Chemistry.

[33]  D. Goodman,et al.  Induction of the expression of retinol-binding protein and transthyretin in F9 embryonal carcinoma cells differentiated to embryoid bodies. , 1988, The Journal of biological chemistry.

[34]  C. Mummery,et al.  Snail is an immediate early target gene of parathyroid hormone related peptide signaling in parietal endoderm formation. , 2000, The International journal of developmental biology.

[35]  J. Rossant,et al.  The transcription factor HNF3beta is required in visceral endoderm for normal primitive streak morphogenesis. , 1998, Development.

[36]  A. Enders,et al.  Comparative aspects of blastocyst-endometrial interactions at implantation. , 1978, Ciba Foundation symposium.

[37]  R. Beddington,et al.  An assessment of the developmental potential of embryonic stem cells in the midgestation mouse embryo. , 1989, Development.

[38]  B. Hogan,et al.  Evidence from molecular cloning that SPARC, a major product of mouse embryo parietal endoderm, is related to an endothelial cell ‘culture shock’ glycoprotein of Mr 43,000. , 1986, The EMBO journal.

[39]  H. Sambrook Molecular cloning : a laboratory manual. Cold Spring Harbor, NY , 1989 .

[40]  R. Beddington,et al.  Msg1 and Mrg1, founding members of a gene family, show distinct patterns of gene expression during mouse embryogenesis , 1998, Mechanisms of Development.

[41]  C. Dickson,et al.  Identification of positive and negative regulatory elements involved in the retinoic acid/cAMP induction of Fgf-3 transcription in F9 cells. , 1993, Nucleic acids research.

[42]  Toru Kita,et al.  Differentiation of embryonic stem cells into cardiac myocytes , 2002 .