Mechanical phenotyping of primary human skeletal stem cells in heterogeneous populations by real-time deformability cytometry

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Miguel Xavier - , University of Southampton, University Hospital Southampton NHS Foundation Trust (Author)
  • Philipp Rosendahl - , Chair of Cellular Machines (Author)
  • Maik Herbig - , Chair of Cellular Machines (Author)
  • Martin Kräter - , University Hospital Carl Gustav Carus Dresden (Author)
  • Daniel Spencer - , University of Southampton (Author)
  • Martin Bornhäuser - , Department of Internal Medicine I, University Hospital Carl Gustav Carus Dresden (Author)
  • Richard O.C. Oreffo - , University Hospital Southampton NHS Foundation Trust (Author)
  • Hywel Morgan - , University of Southampton (Author)
  • Jochen Guck - , Chair of Cellular Machines (Author)
  • Oliver Otto - , Chair of Cellular Machines (Author)

Abstract

Skeletal stem cells (SSCs) are a sub-population of mesenchymal stromal cells (MSCs) present in bone marrow with multipotent differentiation potential. A current unmet challenge hampering their clinical translation remains the isolation of homogeneous populations of SSCs, in vitro, with consistent regeneration and differentiation capacities. Cell stiffness has been shown to play an important role in cell separation using microfluidic techniques such as inertial focusing or deterministic lateral displacement. Here we report that the mechanical properties of SSCs, and of a surrogate human osteosarcoma cell line (MG-63), differ significantly from other cell populations found in the bone marrow. Using real-time deformability cytometry, a recently introduced method for cell mechanical characterization, we demonstrate that both MG-63 and SSCs are stiffer than the three primary leukocyte lineages (lymphocytes, monocytes and granulocytes) and also stiffer than HL-60, a human leukemic progenitor cell line. In addition, we show that SSCs form a mechanically distinct sub-population of MSCs. These results represent an important step towards finding the bio-physical fingerprint of human SSCs that will allow their label-free separation from bone marrow with significant physiological and therapeutic implications.

Details

Original languageEnglish
Pages (from-to)616-623
Number of pages8
JournalIntegrative Biology (United Kingdom)
Volume8
Issue number5
Publication statusPublished - May 2016
Peer-reviewedYes

External IDs

PubMed 26980074

Keywords

ASJC Scopus subject areas