Optimization of the Amplification of Equine Muscle-Derived Mesenchymal Stromal Cells in a Hollow-Fiber Bioreactor.

Julien Duysens, Hélène Graide, Ariane Niesten, Ange Mouithys-Mickalad, Justine Ceusters, Didier Serteyn
Author Information
  1. Julien Duysens: Revatis SA, Rue de la Science 8, 6900 Marche-En-Famenne, Belgium. ORCID
  2. Hélène Graide: Revatis SA, Rue de la Science 8, 6900 Marche-En-Famenne, Belgium.
  3. Ariane Niesten: Centre of Oxygen Research and Development (CORD), University of Liege, 4000 Liege, Belgium.
  4. Ange Mouithys-Mickalad: Centre of Oxygen Research and Development (CORD), University of Liege, 4000 Liege, Belgium. ORCID
  5. Justine Ceusters: Revatis SA, Rue de la Science 8, 6900 Marche-En-Famenne, Belgium.
  6. Didier Serteyn: Revatis SA, Rue de la Science 8, 6900 Marche-En-Famenne, Belgium.

Abstract

The main causes of mortality in horses are the gastrointestinal pathologies associated with septic shock. Stem cells have shown, through systemic injection, a capacity to decrease inflammation and to regenerate injured tissue faster. Nevertheless, to achieve this rapid and total regeneration, systemic injections of 1 to 2 million cells per kilogram of body weight must be considered. Here, we demonstrate for the first time the feasibility and expansion capacity of equine muscle-derived mesenchymal stromal cells (mdMSCs) in a functionally closed, automated, perfusion-based, hollow-fiber bioreactor (HFBR) called the Quantum™ Cell Expansion System (Terumo Blood and Cell Technologies). This feature greatly increases the number of generated cells with a surface area of 1.7 m. The expansion of mdMSCs is very efficient in this bioreactor. The maximum expansion generated twenty times more cells than the initial seeding in nine days. The best returns were observed with an optimal seeding between 10 and 25 million mdMSCs, using the Bull's eye loading method and with a run duration between 7 and 10 days. Moreover, all the generated cells kept their stem properties: the ability to adhere to plastic and to differentiate into chondroblasts, osteoblasts and adipocytes. They also showed the expression of CD-44 and CD-90 markers, with a positive rate above 93%, while CD-45 and MHCII were non-expressed, with a positive rate below 0.5%. By capitalizing on the scalability, automation and 3D culture capabilities of the Quantum™, it is possible to generate large quantities of high-quality equine mdMSCs for gastrointestinal disorders and other clinical applications.

Keywords

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