scholarly journals Large-scale production of lentiviral vector in a closed system hollow fiber bioreactor

2015 ◽  
Vol 2 ◽  
pp. 15020 ◽  
Author(s):  
Jonathan Sheu ◽  
Jim Beltzer ◽  
Brian Fury ◽  
Katarzyna Wilczek ◽  
Steve Tobin ◽  
...  
1994 ◽  
Vol 37 (2) ◽  
pp. 179-184 ◽  
Author(s):  
Sari Ala-Uotila ◽  
Anne Marjamäki ◽  
Marja-Terttu Matikainen ◽  
Markku Jalkanen

1999 ◽  
Vol 22 (4) ◽  
pp. 299-307 ◽  
Author(s):  
Cor H. J. Lamers ◽  
Jan W. Gratama ◽  
Barbara Luider-Vrieling ◽  
Reinder L. H. Bolhuis ◽  
Egbert J. E. G. Bast

Author(s):  
Natalie Rubio ◽  
Isha Datar ◽  
David Stachura ◽  
Kate Krueger

Cellular agriculture is defined as the production of agricultural products from cell cultures rather than from whole plants or animals. With growing interest in cellular agriculture as a means to address the public health, environmental, and animal welfare challenges of animal agriculture, the concept of producing seafood from fish cell- and tissue-cultures is emerging as a means to address similar challenges with industrial aquaculture systems and marine capture. Cell-based seafood - as opposed to animal-based seafood - can combine developments in biomedical engineering with modern aquaculture techniques. Biomedical engineering developments such as closed-system bioreactor production of land animal cells create a basis for large scale production of marine animal cells. Aquaculture techniques such as genetic modification and closed system aquaculture have achieved marked gains in production that can pave the way for innovations in cell-based seafood production. Here, we present the current state of innovation relevant to the development of cell-based seafood across multiple species as well as specific opportunities and challenges that exist for advancing this science. The authors find that the physiological properties of fish cell- and tissue- culture may be uniquely suited to cultivation in vitro. These physiological properties, including hypoxia tolerance, high buffering capacity, and low-temperature growth conditions, make marine cell culture an attractive opportunity for scale production of cell-based seafood; perhaps even more so than mammalian and avian cell cultures for cell-based meats. This, coupled with the unique capabilities of crustacean tissue-friendly scaffolding such as chitosan, a common seafood waste product and mushroom derivative, presents great promise for cell-based seafood production via bioreactor cultivation. To become fully realized, cell-based seafood research will require more understanding of fish muscle culture and cultivation; more investigation into serum-free media formulations optimized for fish cell culture; and bioreactor designs tuned to the needs of fish cells for large scale production.


1990 ◽  
Vol 21 (4) ◽  
pp. 299-309 ◽  
Author(s):  
Soumaya El Ouggouti ◽  
Alain Truskolaski ◽  
Annette Bussel ◽  
Dodier Dhermy ◽  
Olivier Bertrand

2005 ◽  
Vol 7 (6) ◽  
pp. 818-834 ◽  
Author(s):  
Yajin Ni ◽  
Susan Sun ◽  
Ibe Oparaocha ◽  
Laurent Humeau ◽  
Brian Davis ◽  
...  

2003 ◽  
Vol 12 (3) ◽  
pp. 221-228 ◽  
Author(s):  
Jason E. Coleman ◽  
Matthew J. Huentelman ◽  
Sergey Kasparov ◽  
Beverly L. Metcalfe ◽  
Julian F. R. Paton ◽  
...  

The aim of this study was to develop an efficient method for packaging and concentrating lentiviral vectors that consistently yields high-titer virus on a scale suitable for in vivo applications. Transient cotransfection of 293T packaging cells with DNA plasmids encoding lentiviral vector components was optimized using SuperFect, an activated dendrimer-based transfection reagent. The use of SuperFect allowed reproducible and efficient production of high-titer lentiviral vector at concentrations greater than 1 × 107transducing units per ml (TU/ml) and required less than one-third of the total amount of DNA used in traditional calcium phosphate transfection methods. Viral titers were further increased using a novel concentration protocol that yielded an average final titer of 1.4 × 1010TU/ml. Lentiviruses produced using these methods exhibited efficient transduction of central nervous system and peripheral tissues in vivo. The method is reproducible and can be scaled up to facilitate the use of these vectors in animal studies.


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