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Plakoglobin is a mechanoresponsive regulator of naive pluripotency
被引:0
|作者:
Timo N. Kohler
Joachim De Jonghe
Anna L. Ellermann
Ayaka Yanagida
Michael Herger
Erin M. Slatery
Antonia Weberling
Clara Munger
Katrin Fischer
Carla Mulas
Alex Winkel
Connor Ross
Sophie Bergmann
Kristian Franze
Kevin Chalut
Jennifer Nichols
Thorsten E. Boroviak
Florian Hollfelder
机构:
[1] University of Cambridge,Department of Biochemistry
[2] University of Cambridge,Wellcome Trust – Medical Research Council Stem Cell Institute
[3] Jeffrey Cheah Biomedical Centre,Department of Veterinary Anatomy, Graduate School of Agriculture and Life Sciences
[4] The University of Tokyo,Stem Cell Therapy Laboratory, Advanced Research Institute
[5] Tokyo Medical and Dental University,Department of Physiology, Development and Neuroscience
[6] University of Cambridge,Centre for Trophoblast Research
[7] University of Cambridge,Randall Centre for Cell and Molecular Biophysics
[8] King’s College London,MRC Human Genetics Unit, Institute of Genetics and Cancer
[9] The University of Edinburgh,Institute of Medical Physics
[10] Friedrich-Alexander-Universität Erlangen-Nürnberg,Altos Labs
[11] Max-Planck-Zentrum für Physik und Medizin,undefined
[12] Cambridge Institute of Science,undefined
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摘要:
Biomechanical cues are instrumental in guiding embryonic development and cell differentiation. Understanding how these physical stimuli translate into transcriptional programs will provide insight into mechanisms underlying mammalian pre-implantation development. Here, we explore this type of regulation by exerting microenvironmental control over mouse embryonic stem cells. Microfluidic encapsulation of mouse embryonic stem cells in agarose microgels stabilizes the naive pluripotency network and specifically induces expression of Plakoglobin (Jup), a vertebrate homolog of β-catenin. Overexpression of Plakoglobin is sufficient to fully re-establish the naive pluripotency gene regulatory network under metastable pluripotency conditions, as confirmed by single-cell transcriptome profiling. Finally, we find that, in the epiblast, Plakoglobin was exclusively expressed at the blastocyst stage in human and mouse embryos – further strengthening the link between Plakoglobin and naive pluripotency in vivo. Our work reveals Plakoglobin as a mechanosensitive regulator of naive pluripotency and provides a paradigm to interrogate the effects of volumetric confinement on cell-fate transitions.
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