Fiche publication
Date publication
novembre 2021
Journal
Biotechnology and bioengineering
Auteurs
Membres identifiés du Cancéropôle Est :
Dr DE ISLA Natalia
,
Pr OLMOS Eric
Tous les auteurs :
Sion C, Ghannoum D, Ebel B, Gallo F, de Isla N, Guedon E, Chevalot I, Olmos E
Lien Pubmed
Résumé
As a clinical dose requires a minimum of 10 cells per kilogram of patients, it is, therefore, crucial to develop a scalable method of production of Wharton Jelly mesenchymal stem cells (WJ-MSCs) with maintained inner characteristics. Scalable expansion of WJ-MSCs on microcarriers usually found in cell culture, involves specific cell detachment using trypsin and could have harmful effects on cells. In this study, the performance of batch, fed-batch, and perfused-continuous mode of culture were compared. The batch and fed-batch modes resulted in expansion factors of 5 and 43, respectively. The perfused-continuous mode strategy consisted of the implementation of a settling tube inside the bioreactor. The diameter of the tube was calculated to maintain microcarriers colonized by cells in the bioreactor whereas empty microcarriers (responsible for potentially damaging collisions) were removed, using a continuous flow rate based on MSCs physiological requirements. Thanks to this strategy, a maximal number of 800 million cells was obtained in a 1.5 L bioreactor in 10 days. Lastly, online dielectric spectroscopy was implemented in the bioreactor and indicated that cell growth could be monitored during the culture.
Mots clés
dielectric spectroscopy, perfused-continuous mode/marker expression, umbilical cord mesenchymal stem cells
Référence
Biotechnol Bioeng. 2021 11;118(11):4453-4464