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C57bl 6 cd45.1 mice

Manufactured by Jackson ImmunoResearch
Sourced in United States, Montenegro

C57BL/6 CD45.1 mice are a strain of laboratory mice that express the CD45.1 allotype of the CD45 antigen. The CD45 antigen is a protein tyrosine phosphatase that plays a crucial role in the regulation of T and B cell antigen receptor signaling. The CD45.1 allotype is commonly used as a marker to distinguish cells from C57BL/6 mice, which express the CD45.2 allotype.

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33 protocols using c57bl 6 cd45.1 mice

1

Generation of Ezh2 conditional knockout mice

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Ezh2fl/fl mice were obtained from the laboratory of Dr. Tarakhovsky as described22 (link) and were bred with CD4-Cre transgenic mice. These mice were backcrossed with C57BL6 for at least seven generations. Resulting CD4-Cre;Ezh2fl/flmice were further bred to Foxp3-GFP reporter mice to generate Ezh2fl/fl;Foxp3-GFP mice and CD4-Cre;Ezh2fl/fl;Foxp3-GFP mice. CD45.1 C57BL6 mice were from Jackson and Rag2−/− mice were from NIAID mouse facility (Frederick, MD). All animal studies were performed according to the NIH guidelines for the use and care of live animals and were approved by the Institutional Animal Care and Use Committee of NIAMS. All cell cultures were performed in RPMI with 10% fetal calf serum, 2 mM glutamine, 100 IU/ml penicillin, 0.1 mg/ml streptomycin, Hepes buffer (all Invitrogen, CA) and 2 mM β-mercaptoethanol (Sigma, MO).
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2

Lineage Tracing for Hematopoiesis

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All mice were on a C57BL/6 background and were housed at the animal resource center at the University of Chicago. Animal protocols were carried out in accordance with guidelines set by The University of Chicago Institutional Animal Care and Use Committee. Ezh2fl/fl mice were from A. Tarakhovsky (Rockefeller University, New York) (29 (link)). Il7racre mice were from H.-R. Rodewald (Deutsches Krebsforschungszentrum, Heidelberg) (30 (link)). Cdkn2a−/− mice were obtained from the National Cancer Institute (31 (link)). Rosa26LSLYFP and CD45.1 C57BL/6 mice were purchased from Jackson Labs.
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3

Characterization of TRAF6-deficient T Cells

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Mice with a floxed Traf6 gene (Traf6fl/fl mice) on a C57BL/6 background were obtained from Dr. M. Pasparakis (Polykratis et al, 2012). Foxp3yfpCre transgenic mice (originally generated in the laboratory of Dr. Alexander Rudensky) and CD4Cre transgenic mice were obtained from the Jackson Laboratory. These mice were crossed to generate mice specifically lacking TRAF6 in their Tregs and T cells, respectively (Traf6fl/fl Foxp3/CD4Cre+ mice) as well as wild‐type littermate controls (Traf6fl/fl Foxp3/CD4Cre mice). Congenically distinct Thy1.1+ and Thy1.2+ mice on a BALB/c background and CD45.1+ C57BL/6 mice were purchased from the Jackson Laboratory. All mice were housed in a specific‐pathogen‐free facility in accordance with institutional guidelines.
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4

Murine Model of Rift Valley Fever Virus

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All work with infectious RVFV was completed in a biosafety level (BSL)-3 laboratory. Female 6–10-week-old WT C57BL/6 J and CD45.1 C57BL/6 mice were obtained from Jackson Laboratories and housed within ABSL-3 laboratories in microisolator pans in HEPA filtration racks, following standard barrier techniques. In all experiments, mice were evaluated for clinical signs of disease at least once daily and were euthanized according to a predetermined clinical illness scoring algorithm37 (link). At the time of euthanasia, mice were anesthetized with isoflurane and terminally bled. Collected specimens included liver, spleen, brain, popliteal lymph node, and/or whole blood. Splenocytes and other tissues were processed using manual disruption38 (link).
Stocks of recombinant WT RVFV (strain ZH501) and RVFV lacking NSs (DelNSsRVFV) were produced using reverse genetics and grown to passage 212 (link),39 (link). Titers of all viral stocks were determined as the 50% tissue culture infective dose (TCID50) on Vero E6 cells and visualized by indirect fluorescent-antibody assay (IFA) using a monoclonal mouse IgG1 anti-RVFV N primary antibody (custom, Genscript). Virus sequence identity was verified prior to use.
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5

Mouse Immune Cell Trafficking Protocol

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All experiments were approved by the Institutional Animal Care and Use Committee of Ajou University (IACUC No. 2014-0038). WT C57BL/6 mice were purchased from Charles River Laboratories (Orient Bio Inc., Sungnam, Korea). CX3CR1(GFP/+) mice, MyD88 knockout (KO) mice, CD45.1+ C57BL/6 mice and CCR7 KO mice (C57BL/6 background) were purchased from Jackson Laboratories (Bar Harbor, ME). CX3CR1-DTR mice (C57BL/6 background) were kindly provided by Dan R. Littman (New York University Medical Center) and Charles Surh (Pohang University of Science and Technology) (20 (link)). All mice used in the study were at 6 weeks of age. The mice were kept in the Laboratory Animal Research Center of Ajou University Medical Center.
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6

Tracking Antigen-Specific T Cell Responses

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CD45.1+ C57BL/6 mice (six-week-old, female, The Jackson Laboratory, USA) were intravenously transferred with 3 × 105 naïve CD4+ T cells isolated from CD45.2+ OT-II mice. One day later, recipient mice were immunized with PBS, the soluble mixture of OVA and MPLA, or OVA/MPLA MVPs at 10 μg of OVA and 2 μg of MPLA/mouse. One week later, splenocytes from recipients were collected and stained with CD4 (BD 560569) and CD45.2 (BD 561874) for quantification of the percent of transferred CD45.2+ cells among total CD4+ splenocytes using flow cytometry.
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7

Transgenic Mouse Models for Immunological Study

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Zbtb46gfp mice [027618], Cx3cr1CreERT2 mice [020940], Rosa26-stop-TdTomato mice [007914], Cx3cr1GFP/+ mice [005582] and CD45.1+ C57BL/6 mice [002014] were from The Jackson Laboratory. All the mice are in C57BL/6 background. Normal C57BL/6 mice (CD45.2+) were purchased from Shanghai Research Center for Model Organisms. All mice used in this study without specific explanation were 8- to 12-week-old males. Mice were housed in a standard animal facility, with a 12-hr light/dark cycle, in specific-pathogen-free environment. All animal experiments were approved by the Institutional Animal Care and Use Committee at Zhejiang University (protocol ZJU20190135).
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8

Knockout Mouse Models in Immunology

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All experiments with animals in this study were approved by the Purdue Animal Care and Use Committee (PACUC). Rag1(−/−) (B6.129s7-Rag1 tm1Mom/J) mice and IL-10 (−/−) mice were originally from the Jackson laboratory. C57BL/6 mice were originally from Harlan (Indianapolis, IN) and CD45.1 C57BL/6 mice were originally from the Jackson Laboratory. GPR43 (−/−) mice were originally from Deltagen (San Mateo, CA), and GPR41(−/−) mice were obtained from Dr. M. Yanagisawa (UT Southwestern Medical Center at Dallas). All mice were produced at the Purdue Life Science Animal Facility and fed with a regular rodent diet (Purina 5053).
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9

Conditional Ets1 Knockout Mice

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Ets1f/f mice were generated in the University of Chicago Transgenic Core Facility using 129/SvJ embryonic stem cells. The offspring were backcrossed onto the C57BL/6 background for >12 generations. In brief, a targeting vector containing the floxed sites along with exons 8 and 9 containing the Ets1 binding domain was generated and introduced to germline DNA through homologous recombination. After backcrossing, the Ets1f/f mice were crossed to Il7racre mice, which had also been crossed onto the C57BL/6 background for >12 generations (Schlenner et al., 2010 (link)). C57BL/6 Rag1−/− mice and CD45.1+ C57BL/6 mice were purchased through The Jackson Laboratory. All mouse lines were housed at the University of Chicago Animal Resource Center in accordance with the guidelines of the Institutional Animal Care and Use Committee.
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10

Generation of STAT5 Mutant Mice

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STAT5 mutants were generated as described (Yamaji et al., 2013 (link)). Briefly, mice lacking the entire Stat5 locus (Stat5a/b+/-) were crossed with mice lacking one-allele of Stat5a (Stat5a+/- Stat5b+/+) or Stat5b (Stat5a+/+ Stat5b+/-) to produce 8 combinations of Stat5 alleles (Figure 1A). We refer to each genotype according to the total number of Stat5 alleles that are retained. For example, two-allele Stat5a-deficient mice lack both Stat5a alleles but retain two Stat5b alleles (Stat5a-/- Stat5b+/+), while one-allele Stat5a-deficient mice lack both Stat5a alleles but retain one Stat5b allele (Stat5a-/- Stat5b+/-). CD45.1+ C57BL/6 mice were purchased from Jackson Labs (Bar Harbor, ME). Animals were handled in accordance with NIH guidelines and all experiments approved by the NIAMS Animal Care and Use Committee.
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