Implications of Controlled Glycosylation and Apoptosis in Novel Hollow Fiber Bioreactor

Author(s):  
Randal A. Goffe ◽  
Joseph Y. Shi ◽  
Anna K. C. Nguyen
Author(s):  
Aniel Moya-Torres ◽  
Monika Gupta ◽  
Fabian Heide ◽  
Natalie Krahn ◽  
Scott Legare ◽  
...  

Abstract The production of recombinant proteins for functional and biophysical studies, especially in the field of structural determination, still represents a challenge as high quality and quantities are needed to adequately perform experiments. This is in part solved by optimizing protein constructs and expression conditions to maximize the yields in regular flask expression systems. Still, work flow and effort can be substantial with no guarantee to obtain improvements. This study presents a combination of workflows that can be used to dramatically increase protein production and improve processing results, specifically for the extracellular matrix protein Netrin-1. This proteoglycan is an axon guidance cue which interacts with various receptors to initiate downstream signaling cascades affecting cell differentiation, proliferation, metabolism, and survival. We were able to produce large glycoprotein quantities in mammalian cells, which were engineered for protein overexpression and secretion into the media using the controlled environment provided by a hollow fiber bioreactor. Close monitoring of the internal bioreactor conditions allowed for stable production over an extended period of time. In addition to this, Netrin-1 concentrations were monitored in expression media through biolayer interferometry which allowed us to increase Netrin-1 media concentrations tenfold over our current flask systems while preserving excellent protein quality and in solution behavior. Our particular combination of genetic engineering, cell culture system, protein purification, and biophysical characterization permitted us to establish an efficient and continuous production of high-quality protein suitable for structural biology studies that can be translated to various biological systems. Key points • Hollow fiber bioreactor produces substantial yields of homogenous Netrin-1 • Biolayer interferometry allows target protein quantitation in expression media • High production yields in the bioreactor do not impair Netrin-1 proteoglycan quality Graphical abstract


1989 ◽  
Vol 3 (2) ◽  
pp. 139-144 ◽  
Author(s):  
Dong Jin Kim ◽  
Ho Nam Chang ◽  
Jang Ryol Liu

1998 ◽  
pp. 259-266 ◽  
Author(s):  
H. Maerz ◽  
R. Buchholz ◽  
F. Emmrich ◽  
L. Pfeiffer ◽  
U. Marx

Cytotherapy ◽  
2004 ◽  
Vol 6 (4) ◽  
pp. 380-384 ◽  
Author(s):  
A.M. de Kreuk ◽  
A. Zevenbergen ◽  
T. Jonuleit ◽  
G.J. Schuurhuis ◽  
P.C. Huijgens ◽  
...  

2018 ◽  
Vol 4 (1) ◽  
pp. 46-51 ◽  
Author(s):  
Brian Nankervis ◽  
Mark Jones ◽  
Boah Vang ◽  
R. Brent Rice ◽  
Claire Coeshott ◽  
...  

2001 ◽  
Vol 253 (1-2) ◽  
pp. 195-208 ◽  
Author(s):  
Paul J. Yazaki ◽  
Louise Shively ◽  
Cheryl Clark ◽  
Chia-Wei Cheung ◽  
William Le ◽  
...  

2019 ◽  
Vol 36 (2) ◽  
pp. 165-178 ◽  
Author(s):  
Litao Yan ◽  
Xing Wu

AbstractAnimal and clinical studies have shown that mesenchymal stem cells (MSCs) play an important role in cartilage repair. The therapeutic effect of mesenchymal stem cells based therapies has been increasingly demonstrated to exosome-mediated paracrine secretion. Here, we investigated the cellular processes and mechanism of exosomes produced by conventional 2D culture (2D-Exos) and exosomes produced from 3D culture (3D-Exos) of umbilical MSCs (U-MSCs) in a hollow-fiber bioreactor for the treatment of cartilage repair. We found that the yield of 3D-Exos was 7.5-fold higher than that of 2D-Exos. The in vitro experiments indicated that both 2D-Exos and 3D-Exos can stimulate chondrocyte proliferation, migration, and matrix synthesis, and inhibit apoptosis, with 3D-Exos exerting a stronger effect than 2D-Exos. This effect was partly attributed to the activation of transforming growth factor beta 1 and Smad2/3 signaling. The injection of 2D-Exos and 3D-Exos showed enhanced gross appearance and attenuated cartilage defect; however, 3D-Exos showed a superior therapeutic effect than 2D-Exos. In summary, our study provides novel insights into the chondroprotective effects of exosomes produced from 3D culture of U-MSCs in a hollow-fiber bioreactor. Because of its promising biological function and high yield, 3D-Exos may become a promising therapeutic method for the treatment of cartilage defects.


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