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Tnf mice

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Tnf−/− mice are genetically modified mice that lack the tumor necrosis factor (TNF) gene. These mice are commonly used in research to study the role of TNF in various biological processes and disease models.

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7 protocols using tnf mice

1

Transgenic Mouse Models for Dendritic Spine Imaging

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Thy1-YFP-H mice (stock 003782)57 (link), which express yellow fluorescent protein (YFP) in L5 pyramidal neurons, Rosa26-stop-DTR mice (stock 007900)58 (link), which express a conditional DTR-encoding allele in the ROSA locus, Rag1−/− mice (stock 002216)59 (link), Tnf−/− mice (stock 005540)60 (link), Il6−/− mice (stock 002650) and B6 CD45.1 mice (stock 002014) were purchased from the Jackson Laboratory. Cx3cr1CreER mice35 (link) were obtained from the laboratory of Wen-Biao Gan (New York University). Cx3cr1GFP mice34 (link) were obtained from the laboratory of Dan Littman (New York University). To image dendritic spine plasticity in Cx3cr1CreER/+;R26iDTR/+ and Tnf−/− mice, these mice were crossed to Thy1-YFP-H mice. For systemic immune challenge, mice were administered poly(I:C) (Sigma P1530; by i.p. injection) that was dissolved in DPBS. Mice were group-housed in temperature-controlled rooms on a 12-h light–dark cycle and were randomly assigned to different treatment groups. The group size was determined based on previous studies using the same methodologies28 (link),29 (link),30 (link),31 (link),32 (link). Both male and female mice were used. All mice were maintained at the NYU Skirball Institute specific-pathogen-free animal facility and handled in accordance with the institutional guidelines for animal care and use.
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2

Murine Bone Marrow Macrophage Isolation

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All protocols were approved by the Ethical Review Board of Imperial College London, carried out under the authority of the UK Home Office in accordance with the Animals (Scientific Procedures) Act 1986, and reported in compliance with the Animal Research: Reporting ofIn VivoExperiments guidelines (National Centre for the Replacement Refinement & Reduction of Animals in Research, London, United Kingdom). Seventy-six male C57BL/6 mice (Charles River, Wilmington, MA, USA) and 6 TNF−/− mice (The Jackson Laboratory, Bar Harbor, ME, USA) aged between 7 and 8 wk [for bone marrow–derived macrophage (BMDM) harvesting] or 10–14 wk (for in vivo experimentation) were used. Mice were housed in individual ventilated cages (maximum number of 5/cage) and exposed to 12-h light/dark cycles. All experiments were initiated and completed during the light cycle, and no unexpected adverse effects were observed in any of the treatment groups.
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3

Transgenic Mouse Models for Dendritic Spine Imaging

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Thy1-YFP-H mice (stock 003782)57 (link), which express yellow fluorescent protein (YFP) in L5 pyramidal neurons, Rosa26-stop-DTR mice (stock 007900)58 (link), which express a conditional DTR-encoding allele in the ROSA locus, Rag1−/− mice (stock 002216)59 (link), Tnf−/− mice (stock 005540)60 (link), Il6−/− mice (stock 002650) and B6 CD45.1 mice (stock 002014) were purchased from the Jackson Laboratory. Cx3cr1CreER mice35 (link) were obtained from the laboratory of Wen-Biao Gan (New York University). Cx3cr1GFP mice34 (link) were obtained from the laboratory of Dan Littman (New York University). To image dendritic spine plasticity in Cx3cr1CreER/+;R26iDTR/+ and Tnf−/− mice, these mice were crossed to Thy1-YFP-H mice. For systemic immune challenge, mice were administered poly(I:C) (Sigma P1530; by i.p. injection) that was dissolved in DPBS. Mice were group-housed in temperature-controlled rooms on a 12-h light–dark cycle and were randomly assigned to different treatment groups. The group size was determined based on previous studies using the same methodologies28 (link),29 (link),30 (link),31 (link),32 (link). Both male and female mice were used. All mice were maintained at the NYU Skirball Institute specific-pathogen-free animal facility and handled in accordance with the institutional guidelines for animal care and use.
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4

Genetically Modified Mice in Animal Research

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All studies were conducted in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals and the Institutional Animal Care and Use Committee guidelines of the University of Washington and Seattle Biomedical Research Institute where all the work involving animals was conducted. C57BL/6 mice were purchased from Charles River, Wilmington, MA. Il1r1−/− and Tnf−/− mice were purchased from Jackson Laboratory. Casp1−/−11−/− mice were kindly provided by Dr. R. Flavell (Yale University) and described in (Kuida et al., 1995 (link)); Il1a−/−, Il1ab−/− mice were described in (Horai et al., 1998 (link)). Il1b−/− mice were described in (Shornick et al., 1996 (link)). All mice were on C57BL/6 genetic background, matched by age and housed in specific-pathogen-free facilities.
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5

Colitis Experiments in Tnf-/- Mice

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All colitis experiments with animals in this study were approved by the Purdue Animal Care and Use Committee. Six to eight week old, female B6.129S mice with a homozygous deletion of the Tnf gene (Tnf-/- mice) [40 (link)] and control female B6.129S wildtype (WT) mice were obtained from The Jackson Laboratory (Bar Harbor, ME) and subsequently bred and housed at Purdue University. Mice were maintained under specific pathogen free conditions with controlled temperature (21–23°C) and 12/12-hour light/dark cycles. All mice were fed standard mouse chow. Mice were caged separately in 4 groups based on genotype (WT vs Tnf-/-) and treatment (TNBS vs SHAM).
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6

Immunization of WT, TNF−/−, and IL-17R−/− Mice

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Wild type C57Bl/6 and TNF-/- mice on the C57Bl/6 background were purchased from Jackson Laboratories (Bar Harbor, ME). IL-17R-/- mice on the C57Bl/6 background were a gift from Amgen, Seattle [14 (link)]. Mice were immunized with ID93 (0.5 μg) adjuvanted with GLA-SE or GLA-AF (5 μg) via intramuscular injection or intranasal delivery to both nostrils (25 μL total volume). Adjuvants were prepared as described previously [6 (link)]. Mice were anesthetized with ketamine and xylazine prior to intranasal immunization. Mice were immunized 3 times at 3 week intervals. All mice were maintained in specific pathogen-free conditions. After infection animals were maintained in BL3 containment. All procedures were approved by the IDRI institutional animal care and use committee.
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7

Murine Arthritis Model Protocols

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Male and female wild type (WT) C57BL/6 mice were purchased from Harlan (Indianapolis, IN), and were given at least 48 hours to acclimate to the vivarium before use. Other mice were obtained as breeder pairs and were bred/maintained under standard conditions in a University of California, San Diego Animal Facility that is accredited by the American Association for Accreditation of Laboratory Animal Care. KRN T cell receptor transgenic mice were a gift from Drs. D. Mathis and C. Benoist (Harvard Medical School, Boston, MA and Institut de Génétique et de Biologie Moléculaire et Cellulaire, Strasbourg, France). These mice were maintained on a C57BL/6 background (K/B). Arthritic mice were obtained by crossing K/B with NOD/Lt (N) animals (K/BxN). Tnf−/− mice were originally purchased from The Jackson Laboratory (Bar Harbor, Maine, USA).
All animal experiments were conducted according to protocols approved by the Institutional Animal Care and Use Committee of the University of California, San Diego. Mice were housed up to 4 per standard cage at room temperature and maintained on a 12:12 hour light:dark cycle. All behavioral testing was performed during the light cycle. Both food and water were available ad libitum.
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