Part I. Bcl-2 and bcl-xL limit apoptosis upon infection with alphavirus vectors

• Published in: Biotechnology and bioengineering Vol. 67; no. 5; pp. 544 - 554
• Main Authors: Mastrangelo, Alison J., Hardwick, J. Marie, Bex, Françoise, Betenbaugh, Michael J.
• Format: Journal Article
• Language: English
• Published: New York John Wiley & Sons, Inc 05.03.2000; Wiley
• Subjects: Animal cells; apoptosis; Biological and medical sciences; Biotechnology; chloramphenicol acetyltransferase; Eukaryotic cell cultures; Fundamental and applied biological sciences. Psychology; Genetic engineering; Genetic technics; interleukin-12; mammalian cell culture; Methods. Procedures. Technologies; Miscellaneous; Modification of gene expression level; Semliki Forest virus; Sindbis virus; Semliki forest virus; Cell culture; Togaviridae; Gene overexpression; BHK cell line; Recombinant cell; Production; Chloramphenicol O-acetyltransferase; Recombinant protein; Vector; Acyltransferases; Enzyme; Transferases; Rodentia; Interleukin 12; Gene expression; CHO cell line; Sindbis virus; Virus; Infection; Vertebrata; Mammalia; Cell line; Cell death; Animal; Alphavirus; Viability; Hamster; Apoptosis
• ISSN: 0006-3592; 1097-0290
• DOI: 10.1002/(SICI)1097-0290(20000305)67:5<544::AID-BIT5>3.0.CO;2-#

Viral expression systems offer the ability to generate high levels of a particular protein within a relatively short period of time. In particular, alphavirus constructs based on Sindbis virus (SV) and Semliki Forest virus (SFV) are promising vehicles as they are cytoplasmic vectors with the potential for high expression levels. Two such alphavirus vectors were utilized during the current study to infect two commercially relevant cell lines, baby hamster kidney (BHK) and Chinese hamster ovary (CHO); the first was a fully competent SV derivative carrying the gene for chloramphenicol acetyltransferase (dsSV‐CAT), while the second was a replication deficient SFV construct containing the human interleukin‐12 (IL‐12) p35 and p40 genes (SFV‐IL‐12). Since infection with these vectors induced apoptosis in both cell lines, the present effort was dedicated to determining the ability of anti‐apoptosis genes to limit the cell death associated with these virus constructs. Infection with the dsSV‐CAT vector resulted in the rapid death of BHK and CHO cells within 4 days, a phenomenon which was considerably delayed by stably overexpressing bcl‐2 or bcl‐xL. In fact, cellular lifespans were doubled in both BHK‐bcl2 and CHO‐bclxL cells relative to the parental cell lines. Furthermore, the presence of these gene products provided increases of up to 2‐fold in recombinant CAT production. Overexpression of bcl‐2 and bcl‐xL also altered the response of these cells upon infection with SFV‐IL‐12. While the parental cell lines were completely nonviable within 1 week, the BHK‐bcl2, BHK‐bclxL, and CHO‐bclxL cells each recovered from the infection, resuming exponential growth and regaining viabilities of over 90% by 9 days post‐infection. Total IL‐12 productivities were nearly doubled by Bcl‐2 and Bcl‐xL in the CHO cells, although this effect was apparently cell‐line specific, as the native BHK cells were able to secrete more IL‐12 than either of its transfected derivatives. Regardless, the presence of the anti‐apoptosis genes allowed the production of IL‐12 to be maintained, albeit at low levels, from each of the cell lines for the duration of the culture process. Therefore, overexpression of bcl‐2 family members can have a significant impact on culture viabilities and recombinant protein production during alphavirus infections of mammalian cells. © 2000 John Wiley & Sons, Inc. Biotechnol Bioeng 67: 544–554, 2000.