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. 2017 Feb 2;12(2):e0168328. doi: 10.1371/journal.pone.0168328

Fig 4. SOCE is required for HBV replication.

Fig 4

(A and B) Primary rat hepatocytes were loaded with 5 μM Fura-4F and treated with 2 μM TG in Ca2+-free buffer, followed by treatment with DMSO or the SOCE inhibitor 50 μM APB (A) or 100 nM La3+ (B) before the addition of 1 mM CaCl2 (Ca2+). Calculations were performed as described for Fig 3. The data represent the means ± SE and are taken from at least three experiments from different hepatocyte preparations. (C-E) Primary rat hepatocytes were infected with a recombinant adenovirus expressing HBV (AdHBV) and treated with the SOCE inhibitors for 48 hrs or infected with a recombinant adenovirus expressing an HBx-deficient HBV (AdHBV*7). Levels of HBV replication (Southern blot) (C), HBV core protein expression (western blot) (D), and HBV mRNAs (northern blot) (E) were assessed.