Abstract
Typical in vitro barrier and co-culture models rely upon thick semi-permeable polymeric membranes that physically separate two compartments. Polymeric track-etched membranes, while permeable to small molecules, are far from physiological with respect to physical interactions with co-cultured cells and are not compatible with high-resolution imaging due to light scattering and autofluorescence. Here we report on an optically transparent ultrathin membrane with porosity exceeding 20%. We optimize deposition and annealing conditions to create a tensile and robust porous silicon dioxide membrane that is comparable in thickness to the vascular basement membrane (100–300 nm). We demonstrate that human umbilical vein endothelial cells (HUVECs) spread and proliferate on these membranes similarly to control substrates. Additionally, HUVECs are able to transfer cytoplasmic cargo to adipose-derived stem cells when they are co-cultured on opposite sides of the membrane, demonstrating its thickness supports physiologically relevant cellular interactions. Lastly, we confirm that these porous glass membranes are compatible with lift-off processes yielding membrane sheets with an active area of many square centimeters. We believe that these membranes will enable new in vitro barrier and co-culture models while offering dramatically improved visualization compared to conventional alternatives.
Highlights
Membranes are used in cell culture for a variety of applications including cell migration assays [1,2], tissue barrier models [3,4,5] and cellular co-culture systems [6,7,8,9,10,11,12]
human umbilical vein endothelial cells (HUVECs) were grown on three substrates: 0.5 μm low porosity SiO2 membranes, non-porous SiO2 membranes, and tissue culture plastic (TCP)
For monolayer formation studies, HUVEC were grown on 0.5 μm low porosity SiO2 membranes and TCP
Summary
Membranes are used in cell culture for a variety of applications including cell migration assays [1,2], tissue barrier models [3,4,5] and cellular co-culture systems [6,7,8,9,10,11,12]. All SiO2 membranes used in the cell culture studies are chip-supported. A 3.0 μm low porosity SiO2 membrane was used in a cell culture device fabricated as previously described [11]. HUVEC were grown on three substrates: 0.5 μm low porosity SiO2 membranes, non-porous SiO2 membranes, and TCP.
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