Table 3:
Cell Sources | Key Features and Findings | Media Composition | Shear Stress | Culture Support | Reference |
---|---|---|---|---|---|
• Rat primary BECs, astrocytes, and pericytes | • Gravity driven flow • Measured BECs response to TNF-α treatment |
EC growth medium with 20% FBS | 50 – 100 μL hr−1 | Collagen I gel 300 – 400 μm diameter vessel | [40] |
• Human immortalized BECs • Human primary astrocytes |
• Hollow PVDF fibers • Phalloidin stained actin filaments aligned with shear • VEGF, TNF-α, and verapamil increased permeability of tracer |
EC growth medium | 0, 0.77, 3, 17 dyne cm−2 | PDVF fibers 0.1 μm pore size | [37] |
• Human primary BECs, astrocytes, and pericytes | • Large 500 – 700 μm vessels • Incorporation of astrocytes and pericytes decreased tracer permeability • 3D culture increased ability to respond to excitatory stimuli |
EC growth medium | 1 dyne cm−2 | 5 mg mL−1 collagen I gel | [41] |
• Immortalized human BECs • Primary human astrocytes |
• Permeability and TEER measured in vessels • Measured the effect of mechanical deformation of gel on vascular integrity |
EC growth medium | 0.7 dyne cm−2 | 5 mg mL−1 collagen I, 1 mg mL−1 Matrigel, 2 mg mL−1 hyaluronan | [35] |
• hPSC derived BECs | • Determined the role of ECM composition and stiffness in the formation of vessels | EC growth medium | 1 dyne cm−2 | Crosslinked 7 mg mL−1 collagen I gels coated with collagen IV and fibronectin | [38] |
• hPSC derived BMECs | • Measured permeability and efflux activity • Recorded cell proliferation • Displayed transient disruption of BECs due to hyperosmolarity |
EC growth medium | 4 dyne cm−2 | Crosslinked 7 mg mL−1 collagen I gels coated with collagen IV and fibronectin | [36] |
• hPSC derived BMECs • HUVEC |
• Permeability was stable over 2 weeks • Permeability decreased with shear stress |
EC growth medium | 100 μL min−1 | Gelatin and microbial transglutaminase coated with collagen IV and fibronectin | [39] |