mammalian cell cultivation
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Data ◽  
2021 ◽  
Vol 6 (3) ◽  
pp. 23
Author(s):  
Natalia Menshutina ◽  
Elena Guseva ◽  
Diana Batyrgazieva ◽  
Igor Mitrofanov

Over the past few decades, animal cell culture technology has advanced significantly. It is now considered a reliable, functional, and relatively well-developed technology. At present, biotherapeutic drugs are synthesized using cell culture techniques by large manufacturing enterprises that produce products for commercial use and clinical research. The reliable implementation of mammalian cell culture technology requires the optimization of a number of variables, including the culture environment and bioreactor conditions, suitable cell lines, operating costs, efficient process management and, most importantly, quality. Successful implementation also requires an appropriate process development strategy, industrial scale, and characteristics, as well as the certification of sustainable procedures that meet the requirements of current regulations. All of this has led to a trend of increasing research in the field of biotechnology and, as a result, to a great accumulation of scientific information which, however, remains fragmentary and non-systematic. The development of information and network technologies allow us to solve this problem. Information system creation allows for implementation of the modern concept of integrating various structured and unstructured data, as well as the collection of information from internal and external sources. We propose and develop an information system which contains the conditions and various parameters of cultivation processes. The associated ranking system is the result of the set of recommendations—both from technological and hardware solutions—which allow for choosing the optimal conditions for the cultivation of mammalian cells at the stage of scientific research, thereby significantly reducing the time and cost of work. The proposed information system allows for the accumulation of experience regarding existing technologies for the cultivation of mammalian cells, along with application to the development of new technologies. The main goal of the present work is to discuss information systems, the organizational support of scientific research in the field of mammalian cell cultivation, and to provide a detailed description of the developed system and its main modules, including the conceptual and logical scheme of the database.


2020 ◽  
Vol 36 (2) ◽  
Author(s):  
Yuta Okamoto ◽  
Yuji Haraguchi ◽  
Naoya Sawamura ◽  
Toru Asahi ◽  
Tatsuya Shimizu

Author(s):  
Ana Fernandes-Platzgummer ◽  
Sara M. Badenes ◽  
Cláudia L. da Silva ◽  
Joaquim M. S. Cabral

2015 ◽  
Vol 100 (1) ◽  
pp. 113-124 ◽  
Author(s):  
Fabian Stiefel ◽  
Albert Jesuran Paul ◽  
Troisi Jacopo ◽  
Angelo Sgueglia ◽  
Martina Stützle ◽  
...  

2014 ◽  
Vol 95 (1) ◽  
pp. 171-178 ◽  
Author(s):  
Jiyeon Si ◽  
Misoon Kim ◽  
Mi Young Lim ◽  
GwangPyo Ko

Enteric human adenoviruses (HAdVs; serotypes 40 and 41) have been identified as an emerging cause of drinking water contamination. Due to their fastidious characteristics, HAdVs are difficult to cultivate and therefore not detected easily by standard mammalian cell cultivation methods. Here we found that human embryonic kidney 293 cells, transformed transiently with Ras, enhanced HAdV replication by more than threefold. We also constructed a stable cell line overexpressing the Ras protein, 293-Ras, in which the replication of three HAdV strains of serotypes 40 and 41 was increased markedly. However, only HAdV replication was enhanced; infection of 293 and 293-Ras cells with human rhinivorus-6 showed no significant differences in replication rate. Infected 293-Ras cells exhibited an increased level and phosphorylation of extracellular regulated kinase (ERK). In addition, the Ras-mediated increase in HAdV replication was impaired by the mitogen-activated protein kinase/ERK kinase (MEK1) inhibitor U0126, suggesting direct involvement of the MEK1/ERK pathway in enhanced HAdV replication. Based on these results, we suggest that the 293-Ras cell line be used for the efficient detection and cultivation of HAdV strains in both clinical and environmental specimens.


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