scholarly journals Bacterial Nanocellulose as a Scaffold for In Vitro Cell Migration Assay

Nanomaterials ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2322
Author(s):  
Milena Ugrin ◽  
Jelena Dinic ◽  
Sanja Jeremic ◽  
Sandra Dragicevic ◽  
Bojana Banovic Djeri ◽  
...  

Bacterial nanocellulose (BNC) stands out among polymers as a promising biomaterial due to its mechanical strength, hydrophilicity, biocompatibility, biodegradability, low toxicity and renewability. The use of scaffolds based on BNC for 3D cell culture has been previously demonstrated. The study exploited excellent properties of the BNC to develop an efficient and low-cost in vitro cell migration assay. The BNC scaffold was introduced into a cell culture 24 h after the SW480 cells were seeded, and cells were allowed to enter the scaffold within the next 24–48 h. The cells were stained with different fluorophores either before or after the introduction of the scaffold in the culture. Untreated cells were observed to enter the BNC scaffold in significant numbers, form clusters and retain a high viability after 48 h. To validate the assay’s usability for drug development, the treatments of SW480 cells were performed using aspirin, an agent known to reduce the migratory potential of this cell line in culture. This study demonstrates the application of BNC as a scaffold for cell migration testing as a low-cost alternative to commercial assays based on the Boyden chamber principle. The assay could be further developed for routine use in cancer research and anticancer drug development.

2018 ◽  
Vol 186 (3) ◽  
pp. 633-643 ◽  
Author(s):  
Xiaoqing Lv ◽  
Zhaoxin Geng ◽  
Zhiyuan Fan ◽  
Shicai Wang ◽  
WeiHua Pei ◽  
...  

2020 ◽  
Vol 334 ◽  
pp. 110-116
Author(s):  
Emma Bishop ◽  
Damien Breheny ◽  
Katherine Hewitt ◽  
Mark Taylor ◽  
Tomasz Jaunky ◽  
...  

2011 ◽  
Vol 25 (8) ◽  
pp. 2124-2134 ◽  
Author(s):  
B. Rees ◽  
S.W. Spiekstra ◽  
M. Carfi ◽  
K. Ouwehand ◽  
C.A. Williams ◽  
...  

2015 ◽  
Vol 29 (5) ◽  
pp. 997-1005 ◽  
Author(s):  
Götz A. Westphal ◽  
Isabell Schremmer ◽  
Alexander Rostek ◽  
Kateryna Loza ◽  
Nina Rosenkranz ◽  
...  

2013 ◽  
Vol 21 (6) ◽  
pp. 897-903 ◽  
Author(s):  
Min Zhang ◽  
Hongjing Li ◽  
Huipeng Ma ◽  
Jianhua Qin

2020 ◽  
Author(s):  
Giraso Kabandana ◽  
Adam Michael Ratajczak ◽  
Chengpeng Chen

Microfluidic technology has tremendously facilitated the development of in vitro cell cultures and studies. Conventionally, microfluidic devices are fabricated with extensive facilities by well-trained researchers, which hinders the widespread adoption of the technology for broader applications. Enlightened by the fact that low-cost microbore tubing is a natural microfluidic channel, we developed a series of adaptors in a toolkit that can twine, connect, organize, and configure the tubing to produce functional microfluidic units. Three subsets of the toolkit were thoroughly developed: the tubing and scoring tools, the flow adaptors, and the 3D cell culture suite. To demonstrate the usefulness and versatility of the toolkit, we assembled a microfluidic device and successfully applied it for 3D macrophage cultures, flow-based stimulation, and automated near real-time quantitation with new knowledge generated. Overall, we present a new technology that allows simple, fast, and robust assembly of customizable and scalable microfluidic devices with minimal facilities, which is broadly applicable to research that needs or could be enhanced by microfluidics.


1958 ◽  
Vol 41 (5) ◽  
pp. 1027-1034 ◽  
Author(s):  
T. D. C. Grace

1. The ovarian tissues from diapausing pupae of the promethea moth (Callosamia promethea) have survived and grown for 186 days under in vitro conditions. There was continual cell migration and multiplication for a period of 53 days, followed by a period of 47 days during which no cells migrated from the tissues. Between the 100th and 105th days after setting up the cultures, cell migration was resumed, and by the 111th day 250 cells were present in the medium. A few cell divisions were observed between the 126th and 136th days. After the tissues were subcultured on the 140th day, the explant culture continued to survive, but the cell culture died 3 days later. 2. The tissues were subcultured a total of 6 times during the 186 days. By the introduction of a piece of live tissue into the cell cultures, the growth and survival of the cells were increased from 8 days to about 20 days. 3. It is possible that the tissues had become adapted to the medium during their long survival, as the cells which migrated from them after 100 days showed considerably longer survival than those in earlier cultures.


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