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Trypsinization-dependent cell labeling with fluorescent nanoparticles

Trypsin is often used to detach adhered cell subculture from a substrate. However, the proteolytic activity of trypsin may harm cells by cleaving the cell membrane proteins. The present study shows that cellular uptake of fluorescent nanoparticles is remarkably increased within 24 h after trypsiniza...

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Detalles Bibliográficos
Autores principales: Serdiuk, Tetiana, Alekseev, Sergei, Lysenko, Vladimir, Skryshevsky, Valeriy, Géloën, Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199777/
https://www.ncbi.nlm.nih.gov/pubmed/25328505
http://dx.doi.org/10.1186/1556-276X-9-568
Descripción
Sumario:Trypsin is often used to detach adhered cell subculture from a substrate. However, the proteolytic activity of trypsin may harm cells by cleaving the cell membrane proteins. The present study shows that cellular uptake of fluorescent nanoparticles is remarkably increased within 24 h after trypsinization. These results highlight the trypsin-induced protein digestion, provoking leaky cell plasma membrane which leads to the strongly enhanced cellular uptake of the nanoparticles. To prevent this effect, one should expose cells to the nanoparticle (NP)-based fluorescent labels at least 48 h after trypsinization.