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Mechanical stimulation of cyclic tensile strain induces reduction of pluripotent related gene expressions via activation of Rho/ROCK and subsequent decreasing of AKT phosphorylation in human induced pluripotent stem cells
- Source :
- Biochemical and Biophysical Research Communications. 417:836-841
- Publication Year :
- 2012
- Publisher :
- Elsevier BV, 2012.
-
Abstract
- Mechanical stimulation has been shown to regulate the proliferation and differentiation of stem cells. However, the effects of the mechanical stress on the stemness or related molecular mechanisms have not been well determined. Pluripotent stem cells such as embryonic stem (ES) cells and induced pluripotent stem (iPS) cells are used as good materials for cell transplantation therapy and research of mammalian development, since they can self-renew infinitely and differentiate into various cell lineages. Here we demonstrated that the mechanical stimulation to human iPS cells altered alignment of actin fibers and expressions of the pluripotent related genes Nanog, POU5f1 and Sox2. In the mechanically stimulated iPS cells, small GTPase Rho was activated and interestingly, AKT phosphorylation was decreased. Inhibition of Rho-associated kinase ROCK recovered the AKT phosphorylation and the gene expressions. These results clearly suggested that the Rho/ROCK is a potent primary effector of mechanical stress in the pluripotent stem cells and it participates to pluripotency-related signaling cascades as an upper stream regulator.
- Subjects :
- Homeobox protein NANOG
Cellular differentiation
Induced Pluripotent Stem Cells
Biophysics
Biology
Mechanotransduction, Cellular
Biochemistry
SOX2
Tensile Strength
Humans
Phosphorylation
Induced pluripotent stem cell
Molecular Biology
Cells, Cultured
Homeodomain Proteins
rho-Associated Kinases
Induced stem cells
SOXB1 Transcription Factors
Nanog Homeobox Protein
Cell Biology
Embryonic stem cell
Cell biology
Endothelial stem cell
Gene Expression Regulation
Stem cell
Octamer Transcription Factor-3
Proto-Oncogene Proteins c-akt
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 417
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....f1acf916943addae86834d1b92098959
- Full Text :
- https://doi.org/10.1016/j.bbrc.2011.12.052