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5 protocols using il 17a mice

1

Genetic Modulation of Th17 Immunity

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Rag2−/− mice (008449), Tcrδ−/− mice (002120), muMT−/− mice (002288), Tcrα−/− mice (002116), Il17a−/− mice (016879) were from Jackson Lab. Il17f−/− mice were from Dr. Sarah L. Gaffen and Dr.Yoichiro Iwakura’s lab, Il17rc−/− and Il17ra−/− were from Amgen, Il17RCflox/flox mice were from Dr. Jay K. Kolls’ lab31 . Vγ6Vδ1 Tg mice were from Dr. Diane Mathis’ lab. Adiponectin Cre mice (028020) and UCP1 Cre mice (024670) were from Jackson lab32 . VGLUT3-ires-Cre mice were from Dr. Bradford Lowell’s lab33 . TGFβ antibody (Bioxcell # BE0057 Clone 1D11.16.8) and Isotype control antibody (Bioxcell # BE0083) were i.p. injected to WT B6 mice for 3 weeks at 10mg/kg 3 times a week. sb431542 was i.p. injected to WT B6 mice at 4.2mg/kg/day for 3 weeks. All animal studies were approved by the Institutional Animal Care and Use Committee of Beth Israel Deaconess Medical Center.
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2

Repeated Aspiration Model of Fungal Infection

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All animal procedures were approved by the Animal Care and Use Committee of Indiana State University, the host campus of IUSM-Terre Haute. BALB/c or C57BL6/J mice were obtained from Envigo or Jackson Laboratory, IL-17A−/− mice were obtained from Dr. David Wilkes, TCRδ−/− mice aged 5 weeks were obtained from Jackson Laboratory. Mice were allowed to rest 1–4 weeks prior to experiments. A subset of mice were bred at the IUSM-Terre Haute animal facility with offspring used in subsequent experiments at 7–10 weeks of age. For repeated aspiration, suspensions of 2 × 106 conidia were delivered involuntarily as previously described [25 (link)]. After two weeks of twice weekly aspiration, mice were rested for two weeks, when a final aspiration was administered. Mice were euthanized 72 hrs after the final challenge with sodium pentobarbitol, and lungs were perfused with 10 ml phosphate buffered saline (PBS). Bronchoalveolar lavage fluid (BALF) was collected from the perfused lungs as previously described [26 (link)].
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3

Genetic Modulation of Th17 Immunity

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Rag2−/− mice (008449), Tcrδ−/− mice (002120), muMT−/− mice (002288), Tcrα−/− mice (002116), Il17a−/− mice (016879) were from Jackson Lab. Il17f−/− mice were from Dr. Sarah L. Gaffen and Dr.Yoichiro Iwakura’s lab, Il17rc−/− and Il17ra−/− were from Amgen, Il17RCflox/flox mice were from Dr. Jay K. Kolls’ lab31 . Vγ6Vδ1 Tg mice were from Dr. Diane Mathis’ lab. Adiponectin Cre mice (028020) and UCP1 Cre mice (024670) were from Jackson lab32 . VGLUT3-ires-Cre mice were from Dr. Bradford Lowell’s lab33 . TGFβ antibody (Bioxcell # BE0057 Clone 1D11.16.8) and Isotype control antibody (Bioxcell # BE0083) were i.p. injected to WT B6 mice for 3 weeks at 10mg/kg 3 times a week. sb431542 was i.p. injected to WT B6 mice at 4.2mg/kg/day for 3 weeks. All animal studies were approved by the Institutional Animal Care and Use Committee of Beth Israel Deaconess Medical Center.
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4

Streptozotocin-Induced Diabetes in Mice

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CWRU IACUC and LSVAMC ACORP approved the animal protocols employed in this study. C57BL/6J, IL-17A-GFP, and IL-17A−/− mice were obtained from Jackson Laboratories. Diabetes was induced in 8–10 week old male mice by intraperitoneal injections of streptozotocin (60 mg/kg) on 5 consecutive days, as previously described4 (link). Development of diabetes was defined by non-fasted blood glucose concentrations greater than 250 mg/dl and hyperglycemic hemoglobin A1c levels. Insulin (0–0.2 U) was administered as needed to maintain proper body weight.
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5

Influenza A and E. coli Co-infection in Mice

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Male C57BL/6 mice were purchased from the Shanghai Laboratory Animal Center, Chinese Academy of Sciences. IFN-γ−/−, Tcrd−/−, and IL-17A−/− mice were purchased from The Jackson Laboratory. All mice were housed under specific pathogen-free conditions at the School of Life Sciences, University of Science and Technology of China (USTC), and were used at 6–10 wk of age. Animal care and experimental procedures were followed in accordance with the experimental animal guidelines at USTC. Mouse-adapted influenza A/PR/8/34 strain (H1N1) was a gift from H. Meng (Institute of Basic Medicine, Shandong Academy of Medical Sciences, Shandong, China). For influenza infection studies, mice were anesthetized and infected i.n. with 0.1 HA of PR8 in 50 µl sterile saline. E. coli strain was isolated from stool of PR8-infected mice by the 3M Petrifilm E. coli/Coliform Count Plate and was cultured in broth medium for amplification. For E. coli infection, mice were anesthetized and infected i.g. with 5 × 108E.coli in 500 µl sterile saline.
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