In this study, a static magnetic field (SMF) in moderate intensity (10 mT) was employed to investigate its effect on osteoblast and 3T3 fibroblast cell behaviors cultured respectively with magnetic polymer nanofiber mats.
To differentiate between these possibilities, we plated the liquid culture-passaged cells for single colonies and found that telomeres from these clonal isolates were subsets of the heterogeneous liquid-cultured population, a behavior of telomeres that has been reported previously (Shampay and Blackburn, 1988; Levy and Blackburn, 2004).
The biological behavior of cultured human umbilical vein endothelial cells (HUVECs) on Ti O film surfaces was evaluated by an in vitro cultured HUVEC experiment.
The biological behavior of cultured human umbilical vein endothelial cells (HUVECs) onto Ti O film surfaces was evaluated by the in vitro HUVECs cultured experiment.
Multiple culture techniques now exist for the long-term maintenance of neonatal primary murine intestinal organoids in vitro; however, the achievement of contractile behavior within cultured organoids has thus far been infrequent and unpredictable.
In this paper, we synthesized Ti O films using plasma immersion ion implantation and deposition (PIII-D) and investigated the characteristics and the biological behavior of cultured human umbilical vein endothelial cells (HUVEC) onto film surface.
In the present study, poly (ethylene-co-vinyl alcohol) (EVAL) membranes were modified by the covalent bonding of lysine via isocyanation of surface hydroxyl groups to improve cell behavior in cultured cerebellar granule neurons from 7-day-old Wistar rats.
To gain more insight into the effect that the encapsulation of CMPCs in a biomaterial has on their behavior, we cultured CMPCs in unidirectional constrained and stress-free collagen/Matrigel hydrogels.
As there are significant differences in cell behavior when cultured in 1D, 2D, or 3D environments, we hypothesize that migrating cells are also able to sense the dimension of the environment as a guidance cue.
These results, demonstrating differences in cell behavior when cultured on the three different substrates (BM- and AD-ECM and TCP) with differences in chemical and physical properties, provide evidence that the two ECMs may recapitulate specific elements of the native stem cell niche for bone marrow and adipose tissues.
L-MSCs isolated from human fetal lungs demonstrate profound alterations in their phenotype and secretory behavior once cultured in normoxic (21%% O2) and hyperoxic (60%% O2) atmospheres, including rapid differentiation into pro-fibrotic myofibroblasts and reduced production of elastin and certain other ECM components [5].
