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      P19 Cells Overexpressing Lhx1 Differentiate into the Definitive Endoderm by Recapitulating an Embryonic Developmental Pathway

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          Abstract

          Background

          Epiblasts occur at the last pluripotent stage of embryonic development and are important in elucidating how the three germ layers are formed. However, little is known of the molecular mechanisms of their development. We have shown that LIM homeobox 1 (Lhx1) was involved in epiblast development in embryonic stem cells, especially meso- and endodermal differentiation. However, since epiblasts in embryoid bodies spontaneously develop into a further stage, it is difficult to study their development in this system.

          Methods

          Mouse embryonal carcinoma P19 cells which have properties similar to those of epiblasts provided new avenues of investigation into the regulatory mechanism of epiblasts.

          Results

          Overexpression of Lhx1 in P19 cells induced expression of organizer marker genes (Cer1, Gsc) and endoderm marker genes (Gata6, Foxa2, Sox17) but not extra-embryonic endoderm marker genes (Sox7 or Hnf4alpha).

          Conclusion

          This study suggested that Lhx1 overexpression caused P19 cells to differentiate into an endodermal lineage. Thus, P19 cells and their derivatives can be a useful model system to study how the three germ layers are formed.

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          Most cited references17

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          Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells.

          G Martin (1981)
          This report describes the establishment directly from normal preimplantation mouse embryos of a cell line that forms teratocarcinomas when injected into mice. The pluripotency of these embryonic stem cells was demonstrated conclusively by the observation that subclonal cultures, derived from isolated single cells, can differentiate into a wide variety of cell types. Such embryonic stem cells were isolated from inner cell masses of late blastocysts cultured in medium conditioned by an established teratocarcinoma stem cell line. This suggests that such conditioned medium might contain a growth factor that stimulates the proliferation or inhibits the differentiation of normal pluripotent embryonic cells, or both. This method of obtaining embryonic stem cells makes feasible the isolation of pluripotent cells lines from various types of noninbred embryo, including those carrying mutant genes. The availability of such cell lines should made possible new approaches to the study of early mammalian development.
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            Establishment in culture of pluripotential cells from mouse embryos.

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              The in vitro development of blastocyst-derived embryonic stem cell lines: formation of visceral yolk sac, blood islands and myocardium.

              The in vitro developmental potential of mouse blastocyst-derived embryonic stem cell lines has been investigated. From 3 to 8 days of suspension culture the cells form complex embryoid bodies with endoderm, basal lamina, mesoderm and ectoderm. Many are morphologically similar to embryos of the 6- to 8-day egg-cylinder stage. From 8 to 10 days of culture about half of the embryoid bodies expand into large cystic structures containing alphafoetoprotein and transferrin, thus being analagous to the visceral yolk sac of the postimplantation embryo. Approximately one third of the cystic embryoid bodies develop myocardium and when cultured in the presence of human cord serum, 30% develop blood islands, thereby exhibiting a high level of organized development at a very high frequency. Furthermore, most embryonic stem cell lines observed exhibit similar characteristics. The in vitro developmental potential of embryonic stem cell lines and the consistency with which the cells express this potential are presented as aspects which open up new approaches to the investigation of embryogenesis.
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                Author and article information

                Journal
                Yonago Acta Med
                Yonago Acta Med
                YAm
                Yonago Acta Medica
                Tottori University Faculty of Medicine
                0513-5710
                1346-8049
                27 March 2015
                March 2015
                : 58
                : 1
                : 15-22
                Affiliations
                Division of Regenerative Medicine and Therapeutics, Department of Genetic Medicine and Regenerative Therapeutics, Institute of Regenerative Medicine and Biofunction, Tottori University Graduate School of Medical Science, Yonago 683-8503, Japan
                Author notes
                Corresponding author: Yasuaki Shirayoshi, PhD
                Article
                yam-58-015
                4502295
                ae4546ff-6eff-4c0f-97e7-11842cb20fe5
                2015 Yonago Acta medica
                History
                : 8 December 2014
                : 18 December 2014
                Categories
                Original Article
                Custom metadata
                ADE, anterior definitive endoderm; APS, anterior primitive streak; AVE, anterior visceral endoderm; DE, definitive endoderm; DMEM, Dulbecco’s modified Eagle’s medium; EB, embryoid body; EC, embryonal carcinoma; ES, embryonic stem; ExEn, extraembryonic endoderm; FBS, fetal bovine serum; HA, hemagglutinin; HRP, horseradish peroxidase; IgG, immunoglobulin G; KD, knockdown; Lhx1, LIM homeobox 1; MEF, mouse embryonic fibroblast; NEAA, MEM non-essential amino acid solution; O/E, overexpression; PBS, phosphate-buffered saline; PS, primitive streak; PSG, penicillin-streptomycin-L-glutamine solution; qPCR, quantative PCR; RT, reverse transcription; SBE, Smad binding element; TBS-T, Tris-buffered saline with Tween 20; TRC, the RNAi Consortium

                cell differentiation,germ layer,organizer,p19 cells
                cell differentiation, germ layer, organizer, p19 cells

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