Baseline images were taken before 1 μM TG was added. Images were digitally acquired Pexidartinib in vitro every 0.5 to 2 minutes for 20 to 30 minutes with a Nikon TE-200 or Olympus IX-81 epifluorescent microscope. Data were collected from 6 to 14 cells per field and at

least three different fields in different culture wells. All experiments were replicated at least three times. The fluorescence intensity in multiple randomly selected ER locations (for D1ER) or cytosol locations (for YC2.3) at 535 and 485 nm was then determined with Nikon’s Element or MetaMorph 6.3 software. The 535/485 nm or YFP (FRET)/CFP ratio was calculated as the change in the calcium concentration at these locations. In the case of D1ER analysis, we also converted this ratio to the actual calcium Small molecule library manufacturer concentration as previously described.17 Subcellular fractionation of the liver was conducted as described previously.20 Briefly, the postnuclear supernatants of the liver homogenates were centrifuged at 10,000g for 15 minutes. The mitochondria-enriched pellet (P10) was separated from the supernatant (S10), which was further centrifuged at 100,000g for 60 minutes to yield the ER-enriched pellet (P100) and the S100 supernatant. Hepatocytes that were cultured in a 10% serum–containing medium for 24 hours were harvested and incubated in a hypotonic buffer [10 mM 4-(2-hydroxyethyl)-1-piperazine

ethanesulfonic acid (HEPES), pH 7.9, 1.5 mM magnesium dichloride, 10 mM Nitroxoline potassium chloride, and 10 mM phenylmethylsulfonyl fluoride] on ice for 10 minutes before being disrupted with a douncer. The P100 and S100 fractions were obtained as described previously. These fractions were analyzed by an immunoblot assay with the enhanced chemiluminescence method. Images were acquired

with a Kodak MM4000 image station. Multiple-group comparisons were conducted with one-way analysis of variance, whereas paired comparisons were conducted with the Student t test, with P values less than 0.05 being significant. To investigate the mechanism by which Bid regulated hepatocyte proliferation, we stimulated the resting wild-type (WT) and bid-deficient hepatocytes with 10% serum for 24 to 96 hours. The serum contained HGF (released from platelets) as well as low levels of circulating EGF.21 These are the two direct mitogens for hepatocytes. In this system, BrdU incorporation began at 24 hours, peaked at 48 hours, and lasted for 96 hours (Fig. 1A,B) in the WT hepatocytes as previously reported.19 We found that BrdU incorporation in the Bid-deficient hepatocytes did not reach the peak until 72 hours after serum stimulation, and the peak was also at a lower level (Fig. 1A,B). Consistently, we found delayed expression of cyclin D1 and reduced expression of cyclin E in Bid-deficient hepatocytes (Fig. 1C).