Single-cell mechanical phenotype is an intrinsic marker of reprogramming and differentiation along the mouse neural lineage
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
Cellular reprogramming is a dedifferentiation process during which cells continuously undergo phenotypical remodeling. Although the genetic and biochemical details of this remodeling are fairly well understood, little is known about the change in cell mechanical properties during the process. In this study, we investigated changes in the mechanical phenotype of murine fetal neural progenitor cells (fNPCs) during reprogramming to induced pluripotent stem cells (iPSCs). We find that fNPCs become progressively stiffer en route to pluripotency, and that this stiffening is mirrored by iPSCs becoming more compliant during differentiation towards the neural lineage. Furthermore, we show that the mechanical phenotype of iPSCs is comparable with that of embryonic stem cells. These results suggest that mechanical properties of cells are inherent to their developmental stage. They also reveal that pluripotent cells can differentiate towards a more compliant phenotype, which challenges the view that pluripotent stem cells are less stiff than any cells more advanced developmentally. Finally, our study indicates that the cell mechanical phenotype might be utilized as an inherent biophysical marker of pluripotent stem cells.
Details
Original language | English |
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Pages (from-to) | 4313-4321 |
Number of pages | 9 |
Journal | Development (Cambridge) |
Volume | 144 |
Issue number | 23 |
Publication status | Published - 1 Dec 2017 |
Peer-reviewed | Yes |
External IDs
Scopus | 85035806053 |
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Keywords
Keywords
- Animals, Biomarkers/metabolism, Biomechanical Phenomena, CD24 Antigen/metabolism, Cell Differentiation/genetics, Cell Lineage/genetics, Cellular Reprogramming/genetics, Induced Pluripotent Stem Cells/classification, Lewis X Antigen/metabolism, Mice, Mice, Inbred C57BL, Neural Stem Cells/classification, Phenotype, Single-Cell Analysis