Packed Bed Bioreactor for the Isolation and Expansion of Placental-Derived Mesenchymal Stromal Cells

PLoS One. 2015 Dec 14;10(12):e0144941. doi: 10.1371/journal.pone.0144941. eCollection 2015.

Abstract

Large numbers of Mesenchymal stem/stromal cells (MSCs) are required for clinical relevant doses to treat a number of diseases. To economically manufacture these MSCs, an automated bioreactor system will be required. Herein we describe the development of a scalable closed-system, packed bed bioreactor suitable for large-scale MSCs expansion. The packed bed was formed from fused polystyrene pellets that were air plasma treated to endow them with a surface chemistry similar to traditional tissue culture plastic. The packed bed was encased within a gas permeable shell to decouple the medium nutrient supply and gas exchange. This enabled a significant reduction in medium flow rates, thus reducing shear and even facilitating single pass medium exchange. The system was optimised in a small-scale bioreactor format (160 cm2) with murine-derived green fluorescent protein-expressing MSCs, and then scaled-up to a 2800 cm2 format. We demonstrated that placental derived MSCs could be isolated directly within the bioreactor and subsequently expanded. Our results demonstrate that the closed system large-scale packed bed bioreactor is an effective and scalable tool for large-scale isolation and expansion of MSCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipogenesis
  • Animals
  • Bioreactors*
  • Bone Marrow Cells / cytology
  • Cell Culture Techniques / instrumentation*
  • Cell Differentiation
  • Chondrogenesis
  • Female
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Humans
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • Osteogenesis
  • Oxygen / chemistry
  • Oxygen / metabolism
  • Placenta / cytology*
  • Polystyrenes / chemistry
  • Pregnancy

Substances

  • Polystyrenes
  • Green Fluorescent Proteins
  • Oxygen

Grants and funding

This study was funded by Inner Wheel Australia (http://www.innerwheelaustralia.org.au/) and Wound Management Innovation CRC (project 1.06, http://www.woundcrc.com/) awarded to MRD. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.