Loss of Antibody Productivity During Long-Term Cultivation of a Hybridoma Cell Line in Low Serum and Serum-Free Media

Hybridoma ◽  
1990 ◽  
Vol 9 (2) ◽  
pp. 167-175 ◽  
Author(s):  
SADETTIN S. OZTURK ◽  
BERNHARD ØPALSSON
1991 ◽  
Vol 82 (8) ◽  
pp. 883-885 ◽  
Author(s):  
Masanori Terashima ◽  
Kenichiro Ikeda ◽  
Chihaya Maesawa ◽  
Hidenobu Kawamura ◽  
Yorikazu Niitsu ◽  
...  

1988 ◽  
Vol 44 (2) ◽  
pp. 111-121 ◽  
Author(s):  
Ernest H. Helinski ◽  
Kenneth L. Bielat ◽  
Geraldine M. Ovak ◽  
John L. Pauly

2016 ◽  
Vol 39 (4) ◽  
pp. 1421-1432 ◽  
Author(s):  
Jingting Cai ◽  
Tianfang Peng ◽  
Jing Wang ◽  
Jingli Zhang ◽  
Hui Hu ◽  
...  

Background/Aims: Cancer stem cells (CSCs) exhibit enhanced proliferative capacity and resistance to chemotherapy; however, choriocarcinoma CSCs have not yet been reported. In this study the human choriocarcinoma cell line JEG-3 was cultured in serum free media, and the characteristics of suspension and parental adherent JEG-3 cells were compared. Methods: Cell proliferation, colony-formation, soft agar clonogenicity, and transwell invasion assays were performed in vitro, and tumor xenografts in BALB/c nude mice were used to evaluate stem cell properties. Results: In serum-supplemented medium (SSM), JEG-3 cells were 4.51 ± 1.71% CD44+, 7.67 ± 2.67% CD133+, and 13.85 ± 2.95% ABCG2+. In serum-free medium (SFM), the expression of these markers increased to 53.08 ± 3.15%, 47.40 ± 2.67%, and 78.70 ± 7.16%, respectively. Moreover, suspension JEG-3 cells exhibited enhanced colony-formation capability as well as invasive and proliferative ability in vitro, alongside enhanced tumorigenic properties in vivo. Suspension JEG-3 cells also exhibited resistance to the chemotherapeutic drugs methotrexate, fluorouracil and etoposide. When seeded in serum supplemented medium, suspension JEG-3 cells readopted an adherent phenotype and continued to differentiate with no significant difference in the morphology between suspension and parent cells. Conclusion: In this study, choriocarcinoma stem-like cells (CSLCs) were isolated from the human choriocarcinoma JEG-3 cell line by SFM culture and characterized.


Author(s):  
Johann Mols ◽  
Caroline Burteau ◽  
F. Verhoeye ◽  
C. Peeters-Joris ◽  
G. Bastin ◽  
...  

Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 5187-5187
Author(s):  
Sergei Nekhai ◽  
Namita Kumari ◽  
Yuri Obuhkov ◽  
Marina Jerebtsova

Abstract Abstract 5187 Renal glomerular endothelial cells are specialized cells with an important role in physiological filtration and glomerular disease. However, maintenance of human primary endothelial cells requires stimulation with serum and growth factors that often results in modification of the cells properties. Previously, expression of early adenovirus region E4 was shown to help maintaining long-term survival of human endothelial cells in serum free media without addition of growth factors. In the current study, we showed that media conditioned with human epithelial cells stably transfected with Ad E4 region supported survival of human glomerulus-derived endothelial cells in serum-free media (Fig. 1 A and B). Mass-spectrometry analysis of the conditioned media identified pigmental epithelium derived factor (PEDF) as a major component of the conditioned media. PEDF expression in 293-E4 cells was validated by RT- PCR (Fig. 1C), Western Blot and ELISA analysis (Fig. 1D). PEDF expression was detected in mouse glomeruli. Supplementation with recombinant PEDF supported survival of primary endothelial cells and the cells transformed with SV40 large T antigen in serum-free media, and extended the life-span of both cell cultures. PEDF did not inhibit FGF-2 stimulated growth and tubulogenesis of endothelial cells. Thus we demonstrated that adenoviral E4 region stimulated expression and secretion of PEDF by human renal epithelial cells that acted as a survival factor for glomerulus-derived endothelial cells. Acknowledgments: This work was supported NIH Research Grants SC1GM082325, R25 HL003679, 2G12RR003048, 8G12MD007597, K25GM097501 and 1P30HL107253. This study was also supported in part by National Kidney Foundation grant. Disclosures: No relevant conflicts of interest to declare.


2014 ◽  
Vol 50 (9) ◽  
pp. 792-796 ◽  
Author(s):  
Masashi Iwanaga ◽  
Yuka Adachi ◽  
Koudai Uchiyama ◽  
Keita Tsukui ◽  
Susumu Katsuma ◽  
...  
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