And primary cultures of hepatocytes for infection, we utilized human endothelial

And primary cultures of hepatocytes for infection, we utilized human endothelial cells that are highly proliferative. Human umbilical vein endothelial cells were purchased from Lonza (Walkersville, MD), and cultured according to the manufacturer’s instructions. We created a pLNCX (Clontech, Palo Alto, CA)-based vector expressing a dominant-negative form of AKT1 (AKTDN). Retroviral stocks were generated by transient transfection of a packaging cell line (293T, Clontech) and were LED-209 site stored at 280uC until use. Human endothelial cells (passages 4?) were plated at 56105 cells in 10457188 100 mm diameter dishes at 24 hours before infection. Then the culture medium was replaced by retroviral stock supplemented with 8 mg/ml polybrene (Sigma, Tokyo, Japan) for infection. After 48 hours, infected cell populations were selected by 16574785 culture in 500 mg/ml G418 for 7 days. On the 8th day post-infection, 1?36105 infected cells were seeded onto 100 mm diameter dishes. Oxygen consumption rates of cell cultures were determined with a 96-well BD Oxygen Biosensor System plate (BD Biosciences, San Jose, CA).Materials and Methods Animal ModelsAll experiments using live mice were performed in strict accordance with the guidelines of the American Association for Accreditation of Laboratory Animal Care, and the study protocol was approved by Chiba University Institutional Animal Care and Use Committee. Akt1-deficient mice (Akt1+/? were a kind gift from Dr. Morris J. Birnbaum (University of Pennsylvania School of Medicine, Philadelphia, PA). Generation and genotyping of Akt1deficient mice have been described previously [26]. Heterozygous mice were backcrossed with wild-type C57BL/6 mice (SLC, Japan) for 6 generations. All mice were maintained under specificpathogen-free conditions, and their lifespan was monitored by experienced technicians at Sankyo Laboratory Service (n = 101 for wild-type male mice, n = 103 for Akt1+/?male mice, n = 79 for wild-type female mice, n = 80 for Akt1+/?female mice). Survival curves were plotted by the Kaplan eier method, and differences ML 264 web between groups were evaluated by the log-rank test. The maximum lifespan was calculated as the average for the oldest 20 of the mice within each group [27]. For evaluation of the incidence of malignancy, 2-year-old mice were subjected to histopathologic examination by an experienced pathologist (Narabyouri Research Co., Ltd., Japan).Physiological AnalysisWe housed mice individually to monitor their body weight and food intake. Adiposity was examined by CT scanning (LaTheta, Aloka) according to the manufacturer’s protocol. We obtained CT scans at 2 mm intervals from the diaphragm to the floor of the pelvic cavity. Oxygen consumption was measured in 8-week-old and 40-week-old mice with an O2/CO2 metabolic measurement system (Model MK-5000, Muromachikikai), as described previ-Role of Akt1 in LongevityRole of Akt1 in LongevityFigure 2. Pathophysiological features of young and middle-aged female Akt1+/?mice. (A) Body weight of wild-type and Akt1+/?female mice at 14 weeks and 40 weeks old (n = 58). Body weight was lower in Akt1+/?mice. (B) Visceral fat weight per unit body weight of wild-type and Akt1+/?female mice at 8 weeks and 40 weeks old (n = 7). Visceral fat was reduced in Akt1+/?mice. (C) Glucose tolerance of wild-type and Akt1+/?female mice at 8 weeks and 40 weeks old (n = 8). Glucose tolerance did not differ between the two strains. (D) Insulin tolerance of wild-type and Akt1+/?female mice at 40 weeks old (n.And primary cultures of hepatocytes for infection, we utilized human endothelial cells that are highly proliferative. Human umbilical vein endothelial cells were purchased from Lonza (Walkersville, MD), and cultured according to the manufacturer’s instructions. We created a pLNCX (Clontech, Palo Alto, CA)-based vector expressing a dominant-negative form of AKT1 (AKTDN). Retroviral stocks were generated by transient transfection of a packaging cell line (293T, Clontech) and were stored at 280uC until use. Human endothelial cells (passages 4?) were plated at 56105 cells in 10457188 100 mm diameter dishes at 24 hours before infection. Then the culture medium was replaced by retroviral stock supplemented with 8 mg/ml polybrene (Sigma, Tokyo, Japan) for infection. After 48 hours, infected cell populations were selected by 16574785 culture in 500 mg/ml G418 for 7 days. On the 8th day post-infection, 1?36105 infected cells were seeded onto 100 mm diameter dishes. Oxygen consumption rates of cell cultures were determined with a 96-well BD Oxygen Biosensor System plate (BD Biosciences, San Jose, CA).Materials and Methods Animal ModelsAll experiments using live mice were performed in strict accordance with the guidelines of the American Association for Accreditation of Laboratory Animal Care, and the study protocol was approved by Chiba University Institutional Animal Care and Use Committee. Akt1-deficient mice (Akt1+/? were a kind gift from Dr. Morris J. Birnbaum (University of Pennsylvania School of Medicine, Philadelphia, PA). Generation and genotyping of Akt1deficient mice have been described previously [26]. Heterozygous mice were backcrossed with wild-type C57BL/6 mice (SLC, Japan) for 6 generations. All mice were maintained under specificpathogen-free conditions, and their lifespan was monitored by experienced technicians at Sankyo Laboratory Service (n = 101 for wild-type male mice, n = 103 for Akt1+/?male mice, n = 79 for wild-type female mice, n = 80 for Akt1+/?female mice). Survival curves were plotted by the Kaplan eier method, and differences between groups were evaluated by the log-rank test. The maximum lifespan was calculated as the average for the oldest 20 of the mice within each group [27]. For evaluation of the incidence of malignancy, 2-year-old mice were subjected to histopathologic examination by an experienced pathologist (Narabyouri Research Co., Ltd., Japan).Physiological AnalysisWe housed mice individually to monitor their body weight and food intake. Adiposity was examined by CT scanning (LaTheta, Aloka) according to the manufacturer’s protocol. We obtained CT scans at 2 mm intervals from the diaphragm to the floor of the pelvic cavity. Oxygen consumption was measured in 8-week-old and 40-week-old mice with an O2/CO2 metabolic measurement system (Model MK-5000, Muromachikikai), as described previ-Role of Akt1 in LongevityRole of Akt1 in LongevityFigure 2. Pathophysiological features of young and middle-aged female Akt1+/?mice. (A) Body weight of wild-type and Akt1+/?female mice at 14 weeks and 40 weeks old (n = 58). Body weight was lower in Akt1+/?mice. (B) Visceral fat weight per unit body weight of wild-type and Akt1+/?female mice at 8 weeks and 40 weeks old (n = 7). Visceral fat was reduced in Akt1+/?mice. (C) Glucose tolerance of wild-type and Akt1+/?female mice at 8 weeks and 40 weeks old (n = 8). Glucose tolerance did not differ between the two strains. (D) Insulin tolerance of wild-type and Akt1+/?female mice at 40 weeks old (n.