Literature DB >> 21814763

Simultaneous suppression of TGF-β and ERK signaling contributes to the highly efficient and reproducible generation of mouse embryonic stem cells from previously considered refractory and non-permissive strains.

Seyedeh-Nafiseh Hassani1, Mehdi Totonchi, Ali Farrokhi, Adeleh Taei, Mehran Rezaei Larijani, Hamid Gourabi, Hossein Baharvand.   

Abstract

Mouse embryonic stem cells (ESCs) are pluripotent stem cell lines derived from pre-implantation embryos. The efficiency of mESC generation is affected by genetic variation in mice; that is, some mouse strains are refractory or non-permissive to ESC establishment. Developing an efficient method to derive mESCs from strains of various genetic backgrounds should be valuable for establishment of ESCs in various mammalian species. In the present study, we identified dual inhibition of TGF-β and ERK1/2, by SB431542 and PD0325901, respectively led to the highly efficient and reproducible generation of mESC lines from NMRI, C57BL/6, BALB/c, DBA/2, and FVB/N strains, which previously considered refractory or non-permissive for ESC establishment. These mESCs expressed pluripotency markers and retained the capacity to differentiate into derivatives of all three germ layers. The evaluated lines exhibited high rates of chimerism when reintroduced into blastocysts. To our knowledge, this is the first report of efficient (100%) mESC lines generation from different genetic backgrounds. The application of these two inhibitors will not only solve the problems of mESC derivation but also clarifies new signaling pathways in pluripotent mESCs.

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Year:  2012        PMID: 21814763     DOI: 10.1007/s12015-011-9306-y

Source DB:  PubMed          Journal:  Stem Cell Rev Rep        ISSN: 2629-3277            Impact factor:   5.739


  33 in total

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4.  Establishment in culture of pluripotential cells from mouse embryos.

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5.  Suppression of SHP-2 and ERK signalling promotes self-renewal of mouse embryonic stem cells.

Authors:  T Burdon; C Stracey; I Chambers; J Nichols; A Smith
Journal:  Dev Biol       Date:  1999-06-01       Impact factor: 3.582

6.  Nodal signaling regulates the bone morphogenic protein pluripotency pathway in mouse embryonic stem cells.

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7.  A chemical platform for improved induction of human iPSCs.

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8.  Tgfbeta signal inhibition cooperates in the induction of iPSCs and replaces Sox2 and cMyc.

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9.  Efficient derivation of embryonic stem cells by inhibition of glycogen synthase kinase-3.

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  14 in total

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2.  Crosstalk between SOXB1 proteins and WNT/β-catenin signaling in NT2/D1 cells.

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3.  Delay in apoptosome formation attenuates apoptosis in mouse embryonic stem cell differentiation.

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Journal:  J Biol Chem       Date:  2014-04-22       Impact factor: 5.157

4.  Inhibition of transforming growth factor β signaling promotes epiblast formation in mouse embryos.

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Journal:  Stem Cells Dev       Date:  2014-10-29       Impact factor: 3.272

Review 5.  Protein kinases and associated pathways in pluripotent state and lineage differentiation.

Authors:  Melina Shoni; Kathy O Lui; Demetrios G Vavvas; Michael G Muto; Ross S Berkowitz; Nikolaos Vlahos; Shu-Wing Ng
Journal:  Curr Stem Cell Res Ther       Date:  2014       Impact factor: 3.828

6.  Application Of Small Molecules Favoring Naïve Pluripotency during Human Embryonic Stem Cell Derivation.

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Journal:  Cell Reprogram       Date:  2015-06       Impact factor: 1.987

Review 7.  TGF-β and the TGF-β Family: Context-Dependent Roles in Cell and Tissue Physiology.

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8.  Inhibition of TGFβ signaling promotes ground state pluripotency.

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Journal:  Stem Cell Rev Rep       Date:  2014-02       Impact factor: 5.739

9.  Transient Activation of Reprogramming Transcription Factors Using Protein Transduction Facilitates Conversion of Human Fibroblasts Toward Cardiomyocyte-Like Cells.

Authors:  Zaniar Ghazizadeh; Hassan Rassouli; Hananeh Fonoudi; Mehdi Alikhani; Mahmood Talkhabi; Amir Darbandi-Azar; Shuibing Chen; Hossein Baharvand; Nasser Aghdami; Ghasem Hosseini Salekdeh
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10.  Generation of Rat Embryonic Germ Cells via Inhibition of TGFß and MEK Pathways.

Authors:  Alireza Mohammadi; Farnoosh Attari; Vahab Babapour; Seyedeh-Na Seh Hassani; Najmehsadat Masoudi; Abdolhossein Shahverdi; Hossein Baharvand
Journal:  Cell J       Date:  2015-07-11       Impact factor: 2.479

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