Literature DB >> 19002909

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

B H Chun1, S I Chung.   

Abstract

The attachment kinetics of normal and virus-infected LuMA cells were studied to improve the production of live attenuated varicella viruses in human embryonic lung (LuMA) cells. Normal LuMA cells and LuMA cells infected by varicella virus at various cytopathic effects (CPE) were grown on microcarriers. Ninety-three percent of suspended LuMA cells attached to the solid surface microcarriers within fifteen minutes and cell viability was greater than 95% when the cell suspension was stirred. Low serum levels did not affect the attachment rate of virus-infected cells in the microcarrier culture system. Kinetic studies showed that varicella infected cells had a lower attachment rate than normal LuMA cells. Virus inoculum (= infected cells) at low CPE showed a relatively better attachment rate on cell-laden microcarriers than virus inoculum at a higher CPE. Maximum titers were obtained at 2 days post-infection. Based on cell densities, the use of viral inoculum showing a 40% CPE led to an approximately 2- and 1.2-fold increase in the cell associated and in cell free viruses, respectively, than a virus inoculum with a CPE of 10%.However, the ratio of cell-free to cell-associated virus in a microcarrier culture was very low, approximately0.04-0.06. These studies demonstrate that the virus inoculum resulting in a high CPE yielded a high production of cell-associated and cell-free virus in microcarrier cultures because of the high cellular affinity of the varicella virus.

Entities:  

Year:  2001        PMID: 19002909      PMCID: PMC3449971          DOI: 10.1023/A:1016196220750

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


  8 in total

1.  Low-serum medium development for human diploid fibroblast microcarrier cultures.

Authors:  S P Forestell; N Kalogerakis; L A Behie
Journal:  Appl Microbiol Biotechnol       Date:  1992-11       Impact factor: 4.813

2.  Spatial distribution of mammalian cells grown on macroporous microcarriers with improved attachment kinetics.

Authors:  H S Lim; B K Han; J H Kim; M V Peshwa; W S Hu
Journal:  Biotechnol Prog       Date:  1992 Nov-Dec

Review 3.  Microcarrier cell culture.

Authors:  K Nilsson
Journal:  Biotechnol Genet Eng Rev       Date:  1988

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Authors:  A L van Wezel
Journal:  Nature       Date:  1967-10-07       Impact factor: 49.962

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Authors:  J Clark; H Hirstenstein; C Gebb
Journal:  Dev Biol Stand       Date:  1980

6.  Optimizing culture conditions for the production of animal cells in microcarrier culture.

Authors:  J M Clark; M D Hirtenstein
Journal:  Ann N Y Acad Sci       Date:  1981       Impact factor: 5.691

7.  Serial propagation of mammalian cells on gelatin-coated microcarriers.

Authors:  T Y Tao; G Y Ji; W S Hu
Journal:  Biotechnol Bioeng       Date:  1988-10-05       Impact factor: 4.530

8.  Cultivation of mammalian cells on macroporous microcarriers.

Authors:  T J Nikolai; W S Hu
Journal:  Enzyme Microb Technol       Date:  1992-03       Impact factor: 3.493

  8 in total
  2 in total

1.  Comparative investigation of the use of various commercial microcarriers as a substrate for culturing mammalian cells.

Authors:  Duygu Ayyildiz-Tamis; Kamuran Avcı; S Ismet Deliloglu-Gurhan
Journal:  In Vitro Cell Dev Biol Anim       Date:  2013-12-20       Impact factor: 2.416

2.  Expansion and preservation of multipotentiality of rabbit bone-marrow derived mesenchymal stem cells in dextran-based microcarrier spin culture.

Authors:  Lily Boo; Lakshmi Selvaratnam; Cheh Chin Tai; Tunku Sara Ahmad; Tunku Kamarul
Journal:  J Mater Sci Mater Med       Date:  2011-04-02       Impact factor: 3.896

  2 in total

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