Ag - NPs coated with galactose and mannose were considerably less toxic to neuronal - like cells and
hepatocytes compared to particles functionalized by glucose, ethylene glycol or citrate.
Not exact matches
They based their approach on a system they had previously developed for studying the hepatitis C virus, in which they were able to successfully infect human
hepatocytes with the virus and use it to
compare antiviral regimens.
Here, Kate presents her work on that show that culture of human ES cells on human recombinant laminin - 521 and laminin - 111 substrates significantly improve
hepatocyte differentiation, maturation, function and stabilization of phenotype
compared to Matrigel cultured cells.
The Liver - Chip showed improved viability and hepatic function
compared to conventional
hepatocyte culture systems over long - term culture.
To highlight the potentially important role of 3D culture conditions, the authors
compared 2D monolayers of
hepatocyte progenitors, fetal liver stromal cells, or adult bone marrow - derived stromal progenitor cells to their 3D counterparts cultured on liver extracellular matrix (3D - ECM) constructs.
Overall binding of both [3H] TRL preparations was significantly reduced in
hepatocytes isolated from Ldlr — / — Lrp1fl / fl Alb - Cre + mice
compared with
hepatocytes isolated from Ndst1fl / fl Alb - Cre + mice (Figure 10).
Binding and uptake of radiolabeled ApoC - III — depleted TRLs was significantly increased in
hepatocytes isolated from Ndst1fl / fl Alb - Cre + mice (i.e., in mice expressing both LDLR and LRP1) when
compared with ApoC - III — bearing TRLs (Figure 10).
Galactose and mannose - coated nanoparticles were considerably less toxic to both neuronal - like cells Neuro - 2A and
hepatocytes,
compared to particles functionalized with glucose, ethylene glycol or citrate.