Development of PCL-PEG nanofibrous mats as alternative carriers for recombinant Chinese hamster ovary cells

2012 ◽  
Vol 32 (6-7) ◽  
pp. 453-461
Author(s):  
Mehdi Shakibaie ◽  
Marieh Ghafari Rahbar ◽  
Fatemeh Tabandeh ◽  
Hossein Tavanai ◽  
Alireza Zomorodipour ◽  
...  

Abstract In this study, six polyblended nanofiber mats, composed of poly ε-caprolactone (PCL)-polyethylene glycol (PEG) mixed at different proportions in an electrospinning solution were fabricated, and then utilized alongside commercial polyester microcarriers for the mass cultivation of recombinant Chinese hamster ovary (rCHO) cells. The SEM micrographs showed that the rCHO cells were attached to the nanofiber mats with significant differences in their affinities, which can be related to the chemical structure and hydrophilicity of the nanofiber mats. The cell densities of the rCHO cells grown on the polyblended PCL-PEG nanofiber mat (80:20)14% were much higher when compared with the commercial polyester microcarrier. Moreover, recombinant protein production increased by approximately 20% when cells were grown on the PCL-PEG nanofiber mat (80:20)14%. The results of this research indicated a potential for the replacement of the commercial polyester microcarrier with the PCL-PEG polyblended nanofiber mats, in order to achieve mass cultivation of recombinant animal cells in industrial bioreactors.




2017 ◽  
Vol 33 (6) ◽  
pp. 1449-1455 ◽  
Author(s):  
Zhilan Hu ◽  
Wendy Hsu ◽  
Abby Pynn ◽  
Domingos Ng ◽  
Donna Quicho ◽  
...  


1986 ◽  
Vol 103 (4) ◽  
pp. 1159-1166 ◽  
Author(s):  
L D Teeter ◽  
S Atsumi ◽  
S Sen ◽  
T Kuo

Vincristine-resistant (VCR) Chinese hamster ovary (CHO) cells have been established by stepwise selection in increasing concentrations of vincristine. These cells exhibit multidrug cross-resistance to a number of drugs that have no structural or functional similarities. Cytogenetic analyses of resistant cells revealed the presence of double minutes and expanded chromosomal segments, thus implicating gene amplification as a possible mechanism of resistance. An amplified DNA segment isolated from other multidrug cross-resistant CHO cell lines (Roninson, I. B., H. T. Abelson, D. E. Housman, N. Howell, and A. Varshavsky, 1984, Nature (Lond.), 309:626-628) is also amplified in our VCR lines. This DNA segment was used as a probe to screen a cosmid library of VCR genomic DNA, and overlapping clones were retrieved. All of these segments, totaling approximately 45 kilobases (kb), were amplified in VCR cells. Using in situ hybridization, we localized the amplification domain to the long arm of CHO chromosome 1 or Z1. Northern hybridization analysis revealed that a 4.3-kb mRNA was encoded by this amplified DNA domain and was over-produced in the VCR cells. Suggestions for the involvement of these amplified DNA segments in the acquisition of multidrug cross-resistance in animal cells are also presented.



2017 ◽  
Vol 6 (8) ◽  
pp. 1509-1519 ◽  
Author(s):  
Chih-Che Shen ◽  
Li-Yu Sung ◽  
Shih-Yeh Lin ◽  
Mei-Wei Lin ◽  
Yu-Chen Hu


2006 ◽  
Vol 122 (4) ◽  
pp. 463-472 ◽  
Author(s):  
Sung Kwan Yoon ◽  
Jong Kwang Hong ◽  
Seung Ho Choo ◽  
Ji Yong Song ◽  
Hong Woo Park ◽  
...  




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