TY - JOUR
T1 - Impact on monoclonal antibody production in murine hybridoma cell cultures of adenosine receptor antagonists and phosphodiesterase inhibitors
AU - Kelso, Geoffrey F
AU - Kazi, Shahid
AU - Harris, Simon J
AU - Boysen, Reinhard I
AU - Chowdhury, Mohammad
AU - Hearn, Milton T W
PY - 2016/1/15
Y1 - 2016/1/15
N2 - The effects of different adenosine receptor antagonists and cyclic nucleotide phosphodiesterase (PDE) inhibitors on monoclonal antibody (mAb) titer and cell viability of murine hybridoma cells in culture were measured as part of our investigations to discover additives that enhance mAb production. Specific adenosine receptor antagonists and PDE inhibitors were found to enhance or decrease the titer of immunoglobulin G1 (IgG1) mAbs relative to negative controls, depending on the specific compound and cell line employed. The observed enhancements or decreases in IgG1 mAb titer appeared to be mainly due to an increase or decrease in specific productivity rates (ng mAb/cell), respectively. The different effects of the selective adenosine antagonists suggest that antagonism at the level of the adenosine A2A and A1 or the adenosine A3 receptors result in either enhancement or suppression of IgG1 mAb production by hybridoma cells. Overall, these studies have identified hitherto unknown activities of specific adenosine antagonists and PDE inhibitors which indicate they may have valuable roles as cell culture additives in industrial biomanufacturing processes designed to enhance the yields of mAbs or other recombinant proteins produced by mammalian cell culture procedures.
AB - The effects of different adenosine receptor antagonists and cyclic nucleotide phosphodiesterase (PDE) inhibitors on monoclonal antibody (mAb) titer and cell viability of murine hybridoma cells in culture were measured as part of our investigations to discover additives that enhance mAb production. Specific adenosine receptor antagonists and PDE inhibitors were found to enhance or decrease the titer of immunoglobulin G1 (IgG1) mAbs relative to negative controls, depending on the specific compound and cell line employed. The observed enhancements or decreases in IgG1 mAb titer appeared to be mainly due to an increase or decrease in specific productivity rates (ng mAb/cell), respectively. The different effects of the selective adenosine antagonists suggest that antagonism at the level of the adenosine A2A and A1 or the adenosine A3 receptors result in either enhancement or suppression of IgG1 mAb production by hybridoma cells. Overall, these studies have identified hitherto unknown activities of specific adenosine antagonists and PDE inhibitors which indicate they may have valuable roles as cell culture additives in industrial biomanufacturing processes designed to enhance the yields of mAbs or other recombinant proteins produced by mammalian cell culture procedures.
KW - Adenosine antagonist
KW - Hybridoma
KW - Monoclonal antibody
KW - Phosphodiesterase inhibitor
UR - http://www.scopus.com/inward/record.url?scp=84952898646&partnerID=8YFLogxK
UR - http://ac.els-cdn.com.ezproxy.lib.monash.edu.au/S0960894X15302833/1-s2.0-S0960894X15302833-main.pdf?_tid=d587673c-797f-11e6-abaa-00000aacb35d&acdnat=1473750243_577c3dc64a79b2b60aa85c5f03b6e4c5
U2 - 10.1016/j.bmcl.2015.11.075
DO - 10.1016/j.bmcl.2015.11.075
M3 - Article
AN - SCOPUS:84952898646
SN - 0960-894X
VL - 26
SP - 540
EP - 544
JO - Bioorganic and Medicinal Chemistry Letters
JF - Bioorganic and Medicinal Chemistry Letters
IS - 2
ER -