Literature DB >> 18587821

Serial propagation of mammalian cells on gelatin-coated microcarriers.

T Y Tao1, G Y Ji, W S Hu.   

Abstract

The ability to serially propagate mammalian cells in microcarrier cultures is essential for large-scale operation. The success of such serial propagation depends on viable dissociation of cells from microcarriers and the normal growth and product formation after subsequent reinoculation. The high pH treatment developed for dissociating cells from DEAE-derivatized microcarriers was not as effective for a number of cell strains cultivated on gelatin-coated microcarriers. By prewashing the cell-laden microcarriers with buffer containing a chelating agent, bovine kidney cells, BK, human embryonic foreskin fibroblasts, FS-4, and continuous human kidney cells, TCL-598 which produces prourokinase, were viably dissociated from commercially available gelatin-coated microcarriers, Cytodex-3. Cells dissociated from microcarriers reattached and grew on micro-carriers subsequent to inoculation into subcultures. However, after subculturing, cells may attach at different rates to newly added beads and to conditioned microcarriers which cells had previously grown. It resulted in an uneven cell distribution on microcarriers and inferior growth kinetics. This effect was more profound for BK and FS-4 cells which are propagated with a low multiplication ratio. Specifically, BK cells attach to conditioned beads at a faster rate than to new beads, while FS-4 cells attach to new beads faster than to conditioned beads. Thus, for these two cell strains, a separator was used to separate the microcarriers from the suspension of dissociated cells before subsequent inoculation. For TCL-598 cells, which are propagated at a high multiplication ratio, this dissociation technique can be applied directly without the separation of dissociated cells and conditioned microcarriers. All the three cell lines tested exhibit normal growth kinetics in serial propagation on microcarriers. Furthermore, the production of prourokinase by TCL598 cells serially propagated on microcarriers was comparable to that inoculated from roller bottles.

Entities:  

Year:  1988        PMID: 18587821     DOI: 10.1002/bit.260320811

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  4 in total

1.  Expansion and differentiation of human embryonic stem cells to endoderm progeny in a microcarrier stirred-suspension culture.

Authors:  Lye T Lock; Emmanuel S Tzanakakis
Journal:  Tissue Eng Part A       Date:  2009-08       Impact factor: 3.845

2.  Attachment characteristics of normal human cells and virus-infected cells on microcarriers.

Authors:  B H Chun; S I Chung
Journal:  Cytotechnology       Date:  2001-09       Impact factor: 2.058

Review 3.  Scalable stirred-suspension bioreactor culture of human pluripotent stem cells.

Authors:  Daniel E Kehoe; Donghui Jing; Lye T Lock; Emmanuel S Tzanakakis
Journal:  Tissue Eng Part A       Date:  2010-02       Impact factor: 3.845

4.  High-level expression of recombinant human soluble thrombomodulin in serum-free medium by CHO-K1 cells.

Authors:  M Ogata; K Wakita; K Kimura; Y Marumoto; K Oh-i; S Shimizu
Journal:  Appl Microbiol Biotechnol       Date:  1993-01       Impact factor: 4.813

  4 in total

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