Three-dimensional culture of chicken primordial germ cells (cPGCs) in defined media containing the functional polymer FP003
2018
Chen, Yi-Chen | Chang, Wei-Che | Lin, Shau-Ping | Minami, Masataka | Jean, Christian | Hayashi, Hisato | Rival-Gervier, Sylvie | Kanaki, Tatsuro | Wu, Shinn-Chih | Pain, Bertrand | Institute of Biotechnology ; National Taiwan University | Institut cellule souche et cerveau / Stem Cell and Brain Research Institute (SBRI) ; Université Claude Bernard Lyon 1 (UCBL) ; Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE) | Institut National de la Santé et de la Recherche Médicale (INSERM) | Université Claude Bernard Lyon 1 (UCBL) ; Université de Lyon | Department of Animal Science and Technology ; National Taiwan University | Agricultural Biotechnology Research Center ; Academia Sinica | Nissan Chemical Corporation | Council of Agriculture, Executive Yuan, Taiwan [106AS-2.2.2-AD-U1(Z)], [107AS-2.2.2-AD-U1] ; ANR [CRB-ANIM-ANR-11-INBS-0003] | ANR-11-INBS-0003,CRB-Anim,Réseau de Centres de Ressources Biologiques pour les animaux domestiques(2011)
Scalable production of avian cell lines exhibits a valuable potential on therapeutic application by producing recombinant proteins and as the substrate for virus growth due to the special glycosylation occurs in avian species. Chicken primordial germ cells (cPGCs), a germinal pluripotent avian cell type, present the ability of self-renewal, an anchorage-independent cell growth and the ability to be genetically modified. This cell type could be an interesting bioreactor system for industrial purposes. This study sought to establish an expandable culture system with defined components for three-dimensional (3D) culture of cPGCs. cPGCs were cultured in medium supplemented with the functional polymer FP003. Viscoelasticity was low in this medium but cPGCs did not sediment in culture and efficiencies of space and nutrient utilization were thus enhanced and consequently their expansion was improved. The total number of cPGCs increased by 17-fold after 1 week of culture in 3D-FAot medium, an aseric defined medium containing FP003 polymer, FGF2 and Activin A as growth factors and Ovotransferrin as protein. Moreover, cPGC cell lines stably expressed the germline-specific reporter VASA:tdTOMATO, as well as other markers of cPGCs, for more than 1 month upon culture in 3D-FAot medium, indicating that the characteristics of these cells are maintained. In summary, this novel 3D culture system can be used to efficiently expand cPGCs in suspension without mechanical stirring, which is available for long-term culture and no loss of cellular properties was found. This system provides a platform for large-scale culture of cPGCs.
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