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. Author manuscript; available in PMC: 2015 Apr 22.
Published in final edited form as: J Neurochem. 2008 Sep 16;107(2):466–477. doi: 10.1111/j.1471-4159.2008.05618.x

Fig. 2.

Fig. 2

Dose-dependent effect of Aβ1-40 aggregation mixtures on endothelial permeability and TEER in HBMVECs. (a) HBMVEC monolayers grown to confluence on 6.5 mm diameter polycarbonate membrane inserts (0.4 μm pore size) were stimulated via 24 h incubation. Confluent HBMVEC monolayers were incubated with 0, 0.1, 0.3, 1.0, 3.0, 5.0, or 10.0 μmol/L unpurified Aβ1-40 reaction mixture (RH = 65 nm). Values of Pe were calculated as in Fig. 1, and Relative Pe was determined as the ratio of the Pe observed following Aβ1-40 activation to the Pe observed for untreated monolayers. Dependence of Relative Pe upon Aβ1-40 concentration was significant (P < 0.005). Results are representative of at least three independent experiments, performed with three repetitions. Error bars represent SEM. (b) HBMVEC monolayers were grown on 6.5 mm diameter polycarbonate membrane inserts (0.4 μm pore size) in the presence of 550 nmol/L hydrocortisone, and TEER was measured following 0, 1, 2, 3, 4, 5, 6 and 7 days of growth as confluence was reached. At day 7 (arrow), confluent monolayers were incubated alone (○), with 10 Units TNF-α (●), or with 2.5 μmol/L ( Inline graphic), 5.0 μmol/L ( Inline graphic), or 10 μmol/L ( Inline graphic) unpurified Aβ1-40 reaction mixture. TEER was measured following 1, 2, 3, 4, 5, 6, and 7 days of incubation. Results are representative of at least three independent experiments in which TEER measurements were performed with three repetitions. Error bars represent SEM. Some error bars lie within symbols.