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Proteome Analysis of Ground State Pluripotency.
Taleahmad, Sara; Mirzaei, Mehdi; Parker, Lindsay M; Hassani, Seyedeh-Nafiseh; Mollamohammadi, Sepideh; Sharifi-Zarchi, Ali; Haynes, Paul A; Baharvand, Hossein; Salekdeh, Ghasem Hosseini.
Afiliação
  • Taleahmad S; Department of Molecular Systems Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
  • Mirzaei M; Department of Chemistry and Biomolecular sciences, Macquarie University, Sydney, NSW, 2109, Australia.
  • Parker LM; Department of Chemistry and Biomolecular sciences, Macquarie University, Sydney, NSW, 2109, Australia.
  • Hassani SN; ARC Centre of Excellence for Nanoscale BioPhotonics (CNBP), Macquarie University, NSW, 2109, Sydney, Australia.
  • Mollamohammadi S; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
  • Sharifi-Zarchi A; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
  • Haynes PA; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
  • Baharvand H; Department of Chemistry and Biomolecular sciences, Macquarie University, Sydney, NSW, 2109, Australia.
  • Salekdeh GH; ARC Centre of Excellence for Nanoscale BioPhotonics (CNBP), Macquarie University, NSW, 2109, Sydney, Australia.
Sci Rep ; 5: 17985, 2015 Dec 16.
Article em En | MEDLINE | ID: mdl-26671762
ABSTRACT
The differentiation potential of pluripotent embryonic stem cells (ESCs) can be manipulated via serum and medium conditions for direct cellular development or to maintain a naïve ground state. The self-renewal state of ESCs can thus be induced by adding inhibitors of mitogen activated protein kinase (MAPK) and glycogen synthase kinase-3 (Gsk3), known as 2 inhibitors (2i) treatment. We have used a shotgun proteomics approach to investigate differences in protein expressions between 2i- and serum-grown mESCs. The results indicated that 164 proteins were significantly upregulated and 107 proteins downregulated in 2i-grown cells compared to serum. Protein pathways in 2i-grown cells with the highest enrichment were associated with glycolysis and gluconeogenesis. Protein pathways related to organ development were downregulated in 2i-grown cells. In serum-grown ESCs, protein pathways involved in integrin and focal adhesion, and signaling proteins involved in the actin cytoskeleton regulation were enriched. We observed a number of nuclear proteins which were mostly involved in self-renewal maintenance and were expressed at higher levels in 2i compared to serum - Dnmt1, Map2k1, Parp1, Xpo4, Eif3g, Smarca4/Brg1 and Smarcc1/Baf155. Collectively, the results provided an insight into the key protein pathways used by ESCs in the ground state or metastable conditions through 2i or serum culture medium, respectively.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteoma / Células-Tronco Pluripotentes / Proteômica / Células-Tronco Embrionárias Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteoma / Células-Tronco Pluripotentes / Proteômica / Células-Tronco Embrionárias Idioma: En Ano de publicação: 2015 Tipo de documento: Article