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Rag1 mice

Manufactured by Jackson ImmunoResearch
Sourced in Montenegro, United States, Italy

Rag1−/− mice are genetically engineered mice with a mutation in the Rag1 gene, which is essential for the development of mature T and B lymphocytes. These mice lack functional T and B cells, making them a useful model for studying immune system function and development.

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182 protocols using rag1 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

Mouse Models for Tumor Immunology Research

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C57BL/6J WT and Rag1−/− mice were purchased from the Jackson Laboratory and bred in-house. All mice used in experiments were between 2–6 months old. Mice were used according to the protocols approved by the Institutional Animal Use Committee at Northwestern University. B16F10 melanoma and EL4 thymoma cells were obtained from Dr. Hans Schreiber (University of Chicago). B16 cell clones designed to express IL-33 (B16-Vec and B16-IL33) were generated and kindly provided by Dr. Binfeng Lu (University of Pittsburgh) (6 (link)). A tumor cell line was derived from a spontaneous tumor in Jackson lab’s BrafCA, Tyr::CreER and Ptenlox4−5 mouse model, which we have named BPS1 (23 (link)). All cell lines were maintained in complete medium composed of RPMI 1640 containing 5% FBS.
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3

Genetically Engineered Mouse Models

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C57BL6J and Rag1−/− mice were obtained from The Jackson Laboratory, and housed in Umeå University UCCB facility. Ethical approval was acquired from Swedish Board of Agriculture (A39–2017), and animals were housed according to Swedish rules on research and conducted in accordance with the Institutional Animal Care and Use Committee (IACUC) at CSHL. KrasLSL.G12D/+; p53R172H/+; PdxCretg/+ (KPC) mice were bred in-house by pairing heterozygous KrasLSL.G12D/+; p53R172H/+ (KP) mouse with homozygous transgenic Pdx1-Cre (C) mouse. KP mouse were, in turn, bred by pairing KrasLSL.G12D/+ mouse with p53R172H/+ mouse. KP and C mice strains were obtained from The Jackson laboratory.
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4

Mouse Strain Characterization for Research

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Mice between 6–12 weeks old were used. C57Bl/6 mice were from The Jackson Laboratory (Bar Harbor, ME), Taconic Farms (Hudson, NY), or National Cancer Institute (Frederick, MD) or our own breeding colony. RAG1−/− mice and CCR2−/− mice were from Jackson Laboratory. CCR7−/− mice were as described (26 (link)). CCR2−/− mice were bred with CCR7−/− to generate CCR2−/−CCR7−/− mice. IL-1β−/− mice were as described (27 (link)). VEGF-lacZ mice were as described (11 (link), 12 (link), 28 (link)). All animal procedures were performed in accordance with the regulations of the Institutional Animal Use and Care Committee at the Hospital for Special Surgery (New York, NY).
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5

Generating Genetically Modified Mice

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Mice were bred and maintained under specific pathogen-free conditions in accordance with animal facilities at the Seattle Children’s Research Institute (SCRI). Experiments were conducted in accordance with the guidelines of the SCRI Animal Care and Use Committee. IL-23R−/− and DOCK8-deficient (DOCK8pri/pri) mice were generated as previously described 24 (link), 45 (link). WT (C57BL/6) and Rag1−/− mice were purchased from Jackson Laboratories (Bar Harbor, ME) while Rag2−/−IL-2Rγ−/− mice were purchased from Taconic. Most of the animal used in the study were 6 to 8 weeks old male and female mice.
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6

Intracranial Injection of JHMV in Mice

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For intracranial (i.c.) injections, age-matched (5–7 weeks) C57BL/6 miR-155+/+ mice (wildtype (WT)) or miR-155−/− mice were anesthetized with an intraperitoneal (i.p.) injection of 200 μl of a mixture of ketamine (Hospira, Lake Forest, IL, USA) and xylazine (Phoenix Pharmaceutical, Saint Joseph, MO, USA) in Hank’s balanced salt solution (HBSS). Mice were injected intracranially (i.c.) with 200 plaque-forming units (PFU) of JHMV (strain V34) suspended in 30 μl HBSS [39 (link)]. Clinical severity was assessed using a previously described four-point scoring scale [40 (link)]. For analysis of viral titers, mice were sacrificed at indicated time points. One half of each brain was homogenized and used in a plaque assay performed using the DBT mouse astrocytoma cell line [41 (link)]. The DM-JHMV (2.5 × 105 PFU) strain [31 (link), 42 (link)] was used to immunize experimental mice via i.p. injection to generate virus-specific T cells. This is an established and reliable method to accurately measure T cell responses following JHMV infection [42 (link), 43 (link)]. RAG1−/− mice were purchased from Jackson Laboratories. All animal studies were reviewed and approved by the University of Utah Animal Care and Use Committee.
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7

Microbiome Modulation by T Cell Immunity

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C57Bl/6 Myd88LoxP/LoxP mice (Jackson Laboratories) were crossed to C57Bl/6 CD4-Cre animals (Taconic) to produce Myd88+/+; CD4-Cre+ mice (WT) and Myd88LoxP/LoxP; CD4-Cre+ (T-MyD88−/−) animals. Age-matched male mice were used to compare the spontaneous weight phenotype, including immune and microbiota responses, on a standard diet. Age-matched male and female mice were used to compare the weight phenotype, including immune and microbiota responses, on a high-fat diet (HFD). To measure T cell-dependent shaping of the microbiota, 4-week old Tcrb−/− mice (Jackson Laboratories) were used. To investigate Desulfovibrio desulfuricans-dependent shaping of the microbiota, 6-week-old WT C57Bl/6 mice (Jackson Laboratories) were used or age-matched CD4-Cre+ (WT) mice from our facility were used. To measure microbiota effects on weight gain in immunodeficient mice, 4-week old Rag1−/− mice (Jackson Laboratories) were used. GF mice were maintained in sterile isolators and verified monthly for GF status by plating and PCR of feces. GF C57Bl/6 animals were used in this study. The use of animals in all experiments was in strict adherence to federal regulations as well as the guidelines for animal use set forth by the University of Utah Institutional Animal Care and Use Committee.
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8

Murine Models for Immunological Studies

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C57BL/6 (CD45.2+), B6SJL-PTPRC (CD45.1+), OT-I, and Rag1−/− mice were purchased from The Jackson Laboratory. All mice were kept in the animal facility at Fundación Ciencia y Vida and maintained according to the “Guide to Care and Use of Experimental Animals, Canadian Council on Animal Care.” Animal work was carried out under institutional regulations of Fundacion Ciencia & Vida and Facultad de Ciencias, Universidad de Chile and was approved by the local ethics review committees.
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9

Generation of C57BL/6 Rosa-Cas9/Foxp3 Mice

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C57BL/6 Rosa-Cas9/Foxp3Thy1.1 mice were generated by crossing Rosa26-LSL-Cas9 mice (Platt et al., 2014 (link)) (The Jackson Laboratory #024857) with Foxp3Thy1.1 reporter mice (Liston et al., 2008 (link)). Male Cas9/Foxp3Thy1.1 mice at 8-12 weeks age were used to isolate Treg cells for the CRISPR screen, and no gender preference was given for other experiments. C57BL.6 Ly5.1+ congenic mice and Rag1−/− mice purchased from the Jackson Laboratory were used for Treg suppression assay and adoptive T cell transfer in colitis and tumor models. All mice were bred and housed in the specific pathogen-free facilities at the Salk Institute for Biological Studies and were conducted under the regulation of the Institutional Animal Care and Use Committee (IACUC) and institutional guidelines.
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10

Transgenic Mouse Models in Neuroscience

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C57BL/6 mice, Tcra−/− mice, and Rag1−/− mice were obtained from Jackson Laboratories. Aqp4−/− mice were kindly provided by A. Verkman (University of California, San Francisco UCSF) and have been described before [24 (link)]. All mice were housed in a pathogen-free facility at the Technical University of Munich. All experimental protocols were approved by the standing committee for experimentation with laboratory animals of the Bavarian or Rhine Palatinate state authorities and carried out in accordance with the corresponding guidelines (AZ 55.2-1-54-2532-29-13 and 55.2-1-54-2532-95-2014).
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