An ex vivo approach to the differential parenchymal responses induced by cigarette whole smoke and its vapor phase

Toxicology ◽  
2012 ◽  
Vol 293 (1-3) ◽  
pp. 125-131 ◽  
Author(s):  
James Chi-Jen Lin ◽  
Jean-Philippe Roy ◽  
Jules Verreault ◽  
Sébastien Talbot ◽  
France Côté ◽  
...  
2021 ◽  
Vol 72 ◽  
pp. 105099
Author(s):  
Lorena Polloni ◽  
Fernanda Van Petten Vasconcelos Azevedo ◽  
Samuel Cota Teixeira ◽  
Eloá Moura ◽  
Tassia Rafaela Costa ◽  
...  

Author(s):  
Sébastien Baekelandt ◽  
Valérie Cornet ◽  
Syaghalirwa.N.M. Mandiki ◽  
Lambert Jérôme ◽  
Dubois Mickaël ◽  
...  

Cells ◽  
2021 ◽  
Vol 10 (1) ◽  
pp. 132
Author(s):  
Johanna Simon ◽  
Gabor Kuhn ◽  
Michael Fichter ◽  
Stephan Gehring ◽  
Katharina Landfester ◽  
...  

Understanding the behavior of nanoparticles upon contact with a physiological environment is of urgent need in order to improve their properties for a successful therapeutic application. Most commonly, the interaction of nanoparticles with plasma proteins are studied under in vitro conditions. However, this has been shown to not reflect the complex situation after in vivo administration. Therefore, here we focused on the investigation of magnetic nanoparticles with blood proteins under in vivo conditions. Importantly, we observed a radically different proteome in vivo in comparison to the in vitro situation underlining the significance of in vivo protein corona studies. Next to this, we found that the in vivo corona profile does not significantly change over time. To mimic the in vivo situation, we established an approach, which we termed “ex vivo” as it uses whole blood freshly prepared from an animal. Overall, we present a comprehensive analysis focusing on the interaction between nanoparticles and blood proteins under in vivo conditions and how to mimic this situation with our ex vivo approach. This knowledge is needed to characterize the true biological identity of nanoparticles.


2010 ◽  
Vol 196 ◽  
pp. S232-S233
Author(s):  
P. Pinton ◽  
D. Tsybulskyy ◽  
B. Joly ◽  
N. Bourges-Abella ◽  
I.P. Oswald ◽  
...  

Viruses ◽  
2018 ◽  
Vol 10 (8) ◽  
pp. 423 ◽  
Author(s):  
Eva Zusinaite ◽  
Aleksandr Ianevski ◽  
Diana Niukkanen ◽  
Minna Poranen ◽  
Magnar Bjørås ◽  
...  

There are dozens of approved, investigational and experimental antiviral agents. Many of these agents cause serious side effects, which can only be revealed after drug administration. Identification of the side effects prior to drug administration is challenging. Here we describe an ex vivo approach for studying immuno- and neuro-modulatory properties of antiviral agents, which may be associated with potential side effects of these therapeutics. The current approach combines drug toxicity/efficacy tests and transcriptomics, which is followed by mRNA, cytokine and metabolite profiling. We demonstrated the utility of this approach with several examples of antiviral agents. We also showed that the approach can utilize different immune stimuli and cell types. It can also include other omics techniques, such as genomics and epigenomics, to allow identification of individual markers associated with adverse reactions to antivirals with immuno- and neuro-modulatory properties.


2017 ◽  
Vol 18 (2) ◽  
pp. 356 ◽  
Author(s):  
Xuan-Bac Nguyen ◽  
Stanislav Kislyuk ◽  
Duc-Hung Pham ◽  
Angela Kecskés ◽  
Jan Maes ◽  
...  

2000 ◽  
Vol 9 (2) ◽  
pp. 169-178 ◽  
Author(s):  
Bas Blits ◽  
Paul A. Dijkhuizen ◽  
Wim T. J. M. C. Hermens ◽  
Lisette K. E. Van Esseveldt ◽  
Gerard J. Boer ◽  
...  

Regeneration of injured axons following injury depends on a delicate balance between growth-promoting and growth-inhibiting factors. Overexpression of neurotrophin genes seems a promising strategy to promote regeneration. Trophic genes can be overexpressed at the site of injury at the axonal stumps, or at the perikaryal level of the injured neuron. Transduction of the neural cells can be achieved by applying adenoviral vectors, either directly in vivo or—in the case of neurotransplantation—as an ex vivo approach. In both cases it would create a more permissive environment for axonal growth and therefore in functional regeneration. In this article, the feasibility of the use of adenoviral vectors in several neuroregeneration models–-in particularly in spinal cord lesion models and the biological clock transplantation model–-is illustrated. The results show that the adenoviral vectors can be a powerful tool to study the effects of overexpression of genes in an in vivo paradigm of nerve regeneration or nerve outgrowth. The potential use of adenoviral vectors and ex vivo transduced neurotransplants is discussed.


2011 ◽  
Vol 60 (1) ◽  
pp. 522-532 ◽  
Author(s):  
Hsin-Ling Yang ◽  
Ssu-Ching Chen ◽  
K. J. Senthil Kumar ◽  
Kang-Ni Yu ◽  
Pei-Dawn Lee Chao ◽  
...  

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