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. 2016 Feb 11;36(5):862–890. doi: 10.1177/0271678X16630991

Table 8.

Porcine in-vitro models of the blood–brain barrier. Morphology, tightness and astrocyte/pericyte induction.

Model type Endothelial morphology Junction Claudins ∼TEER (Ohm · cm2) (mean values) Permeability 10−6 (cm/s) Occludin/ ZO proteins Astrocyte induction Pericyte induction Selected key references
Primary porcine BCEC (isolation with enzymes) Cobblestone 5 (ICC,mRNA) 250–790 6 (sucrose) Occludin (ICC,mRNA) Increased TEER and changed morphology by astrocyte co-culture 54,106,215
Primary porcine BCEC (isolation including density centrifugation step) Intermediate 5 (ICC,WB) 400–1500 0.6–1 (sucrose) 1.8 (mannitol) ZO1 and Occludin, (ICC,WB) Increased TEER and claudin-5 expression, decrease in Psucrose and changed morphology by astrocyte co-culture Decrease in TEER by pericyte co-culture. However increase in TEER by co-culture with bFGF-treated pericytes. Increase in TEER by porcine pericytes in contact-co-culture 92,104, 213,218–221
Primary porcine BCEC in co-culture with rat astrocytes or astrocyte cell line Cobblestone in mono-culture, change to spindle in co-culture. Intermediate in both mono and co-culture 5 (ICC,WB) 800–1800 0.6 (Lucifer yellow) ZO1 and Occludin (ICC, WB) Increased TEER and claudin-5 expression, decrease in Psucrose and PLY and changed morphology by astrocyte co-culture 54,92,215

: not investigated; ICC: immunocytochemistry; WB: Western blotting.

Note: The permeability value of the smallest tested compound in the study is given.