| Literature DB >> 7764575 |
K Watanabe1, Y Eto, S Takano, S Nakamori, H Shibai, S Yamanaka.
Abstract
A new substrate for mammalian cell culture was developed using a cellulose membrane produced by Acetobacter aceti. Modification of the ionic charge of the membrane and adsorption of collagen to it promoted cellular adhesion to the membrane surface. The growth of eight kinds of cells on the membrane, was comparable to that achieved in plastic Petri dishes. The membrane was tested for use in the production of recombinant Erythroid Differentiation Factor (EDF)/activin A using genetically engineered Chinese hamster ovary cells. Both the viability of the cells and production of EDF/activin A were maintained for about 1 month, while cultures on plastic dishes lasted only 12 days. It was considered that the mechanism of improved cell viability was related to the ultrastructure of the cellulose membrane.Entities:
Mesh:
Substances:
Year: 1993 PMID: 7764575 DOI: 10.1007/BF00749937
Source DB: PubMed Journal: Cytotechnology ISSN: 0920-9069 Impact factor: 2.058