Literature DB >> 1367253

Development of a serum-free and heat-sterilizable medium and continuous high-density cell culture.

Y Minamoto1, K Ogawa, H Abe, Y Iochi, K Mitsugi.   

Abstract

We tried to establish a new serum-free and heat-sterilizable medium, based on our serum-free medium in which many lymphoblastoid cells and hybridoma could grow as well as in a conventional serum-containing medium. As is well-known, L-glutamine (L-Gln) is one of the most heat-labile but essential components for cell growth. As a substitute for L-Gln, dipeptide such as Gly-L-Gln or L-Ala-L-Gln, which was quite stable even after autoclaving, was found to be utilizable for mammalian cell growth. The L-Gln dipeptide-containing serum-free medium was quite stable in a solution even after storing at 37 degrees C for 4 months. In the serum-free medium containing L-Ala-L-Gln, mouse hybridola could grow and produce more antibody than in RPMI 1640 + 10% FBS. It has been proved that BSA and transferrin, which are also heat-labile but essential for the growth of various cell lines, can be substituted by heat-stable alpha-cyclodextrin and cholesterol, and Fe-gluconate, respectively. Insulin has also proved to be heat stable in a solution of Fe-gluconate. We thus established a new serum-free medium, all the components of which could be heat-sterilizable. Moreover, by adding EGF and BSA but without the adhesion factor included in FBS, the serum-free medium was found to support a long-term serial culture of a human diploid fibroblast. Finally, with this auotoclavable serum-free medium in a perfusion culture apparatus, we were able to continuously cultivate a human lymphoblastoid cell line. The production rate of IgM was found to be markedly increased by feeding the serum-free medium enriched by glucose, bicarbonate, L-Cys, and approtinin. The cell density reached as high as 2 x 10(8)/ml in the serum-free medium. Although the working volume in the reactor was only 1 1, the rate of IgM production reached 480 mg/day. The new heat-sterilizable serum-free medium has several advantages, because L-Gln peptide is a heat-stable and available precursor of L-Gln.

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Year:  1991        PMID: 1367253

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  6 in total

1.  Modification of glucose and glutamine metabolism in hybridoma cells through metabolic engineering.

Authors:  C Paredes; E Prats; J J Cairó; F Azorín; L Cornudella; F Gòdia
Journal:  Cytotechnology       Date:  1999-07       Impact factor: 2.058

2.  Promoting effect of rapeseed proteins and peptides on Sf9 insect cell growth.

Authors:  V Deparis; C Durrieu; M Schweizer; I Marc; J L Goergen; I Chevalot; A Marc
Journal:  Cytotechnology       Date:  2003-07       Impact factor: 2.058

3.  Clostridium difficile toxin A induces intestinal epithelial cell apoptosis and damage: role of Gln and Ala-Gln in toxin A effects.

Authors:  Gerly A C Brito; Benedito Carneiro-Filho; Reinaldo B Oriá; Raul V Destura; Aldo A M Lima; Richard L Guerrant
Journal:  Dig Dis Sci       Date:  2005-07       Impact factor: 3.199

4.  Advantages of AlaGln as an additive to cell culture medium: use with anti-CD20 chimeric antibody-producing POTELLIGENT™ CHO cell lines.

Authors:  Yasufumi Imamoto; Hisaya Tanaka; Ken Takahashi; Yoshinobu Konno; Toshiyuki Suzawa
Journal:  Cytotechnology       Date:  2012-06-14       Impact factor: 2.058

5.  CHO cell growth and recombinant interferon-γ production: Effects of BSA, Pluronic and lipids.

Authors:  P M Castro; A P Ison; P M Hayter; A T Bull
Journal:  Cytotechnology       Date:  1995-01       Impact factor: 2.058

6.  Complement susceptibility in glutamine deprived breast cancer cells.

Authors:  Bradley S Ellison; Mary Kb Zanin; Robert J Boackle
Journal:  Cell Div       Date:  2007-07-11       Impact factor: 5.130

  6 in total

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