In vitro,
endothelial cells plated on Matrigel align themselves forming cords, already evident a few hours after plating.
In vitro,
endothelial cells plated on Matrigel align themselves forming cords (Figure 5, C −, negative controls).
Endothelial cells plated onto two - chamber slides at a density of 2 × 105 cells / well in 10 % DMEM were incubated overnight.
Similar to cells growing at 33 °C,
endothelial cells plated in the 37 °C environment also engaged in cell division during the first 24 h. However, during the next 72 h, the growth of most endothelial cells in 37 °C conditions dropped to 50 % of that of their counterparts growing at 33 °C (data not shown).
Not exact matches
Endothelial cells (passage 5) from each line were
plated onto 96 - well
plates at a density of 1000
cells / well in 10 % DMEM.
Matrigel - containing
plates were allowed to incubate at 37 °C for 30 min and then seeded with
endothelial cells at a density of 4 × 104
cells / well in 10 % DMEM.
The onset of tube structure formation could be visualized as early as 4 h after
plating for most
endothelial cell lines, with extensive networks becoming visible within 12 h after
plating.
Briefly, single -
cell suspensions of C57BL / 6 KO and wild - type lymphocytes, which had undergone a 96 hr in vitro boost with γ - irradiated (3,000 rad) BALB / c stimulator lymphocytes, were added to 96 - well microtiter
plates (Corning Inc., Corning, NY) along with 2 × 104 51Cr - labeled BALB / c corneal epithelial or
endothelial cells in a total volume of 200 μl / well.
For induction of differentiation to mature
endothelial cells, EPCs were
plated at a high
cell density (8 × 104
cells / cm2) on tissue culture treated flasks.