Single-cell mechanical phenotype is an intrinsic marker of reprogramming and differentiation along the mouse neural lineage

Marta Urbanska*, Maria Winzi, Katrin Neumann, Shada Abuhattum, Philipp Rosendahl, Paul Müller, Anna Taubenberger, Konstantinos Anastassiadis, Jochen Guck

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

30 Citations (Scopus)

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 stemcells are less stiff than any cells more advanced developmentally. Finally, our study indicates that the cellmechanical phenotypemight be utilized as an inherent biophysical marker of pluripotent stem cells.

Original languageEnglish
Pages (from-to)4313-4321
Number of pages9
JournalDevelopment (Cambridge)
Volume144
Issue number23
DOIs
Publication statusPublished - 1 Dec 2017
Externally publishedYes

Keywords

  • AFM
  • Cell mechanics
  • IPSC
  • NPC
  • Pluripotency
  • Real-time deformability cytometry

Fingerprint

Dive into the research topics of 'Single-cell mechanical phenotype is an intrinsic marker of reprogramming and differentiation along the mouse neural lineage'. Together they form a unique fingerprint.

Cite this