B-HLA-A11.1 mice
| Strain Name | C57BL/6JNifdc-B2mtm1(B2M/HLA-A11.1/H2-D)Bcgen/Bcgen | Common Name | B-HLA-A11.1 mice |
| Background | C57BL/6JNifdc | Catalog number |
112803 |
|
Aliases |
B2M: IMD43 HLA-A: HLAA |
||
模型验证
Protein expression analysis
Analysis of leukocytes cell subpopulation in spleen
Analysis of T cell subpopulation in spleen
Analysis of leukocytes cell subpopulation in lymph node
Analysis of T cell subpopulation in lymph node
Analysis of leukocytes cell subpopulation in blood
Analysis of T cell subpopulation in blood
Identification of target peptide specific TCRs from B-HLA-A11.1 mice
Biochemistry analysis
Gross anatomy of female B-HLA-A11.1 mice
Gross anatomy of male B-HLA-A11.1 mice
Organ weight
Histopathological analysis
Strain specific B2M and HLA-A expression analysis in homozygous B-HLA-A11.1 mice by flow cytometry. Splenocytes were collected from wild-type C57BL/6 mice (+/+) and homozygous B-HLA-A11.1 mice (H/H) and analyzed by flow cytometry with species-specific anti-B2M and anti-HLA-A antibodies. Mouse B2M and H-2Db were detectable in wild-type C57BL/6 mice. Human B2M and HLA-A11.1 were exclusively detectable in homozygous B-HLA-A11.1 mice but not in wild-type mice.
Analysis of spleen leukocyte subpopulations by FACS. Splenocytes were isolated from female C57BL/6 and B-HLA-A11.1 mice (n=3, 8-week-old). Flow cytometry analysis of the splenocytes was performed to assess leukocyte subpopulations. A. Representative FACS plots. Single live cells were gated for the CD45+ population and used for further analysis as indicated here. B. Results of FACS analysis. Percent of total T cells, B cells, NK cells, dendritic cells, granulocytes, monocytes and macrophages in homozygous B-HLA-A11.1 mice were similar to those in the C57BL/6 mice. Percent of CD8+ T cells were significantly decreased, demonstrating that introduction of hB2M-HLA-A11.1-H-2D in place of mouse B2M may affected the development of CD8 + T cells, which in turn affected the proportion of T cell subtypes in the spleen. Values are expressed as mean ± SEM.
Analysis of spleen T cell subpopulations by FACS. Splenocytes were isolated from female C57BL/6 and B-HLA-A11.1 mice (n=3, 8-week-old). Flow cytometry analysis of the splenocytes was performed to assess leukocyte subpopulations. A. Representative FACS plots. Single live CD45+ cells were gated for TCRβ+ T cell population and used for further analysis as indicated here. B. Results of FACS analysis. The percent of Tregs in homozygous B-HLA-A11.1 mice were similar to those in the C57BL/6 mice. Percent of CD8+ T cells were significantly decreased while percent of CD4+ T cells were significantly increased, demonstrating that introduction of hB2M-HLA-A11.1-H-2D in place of mouse B2M may affected the development of CD8 + T cells, which in turn affected the proportion of T cell subtypes in the spleen. Values are expressed as mean ± SEM.
Analysis of lymph node leukocyte subpopulations by FACS. Lymph nodes were isolated from female C57BL/6 and B-HLA-A11.1 mice (n=3, 8-week-old). Flow cytometry analysis of the splenocytes was performed to assess leukocyte subpopulations. A. Representative FACS plots. Single live cells were gated for the CD45+ population and used for further analysis as indicated here. B. Results of FACS analysis. Percent of total T cells, B cells, NK cells, dendritic cells, granulocytes, monocytes and macrophages in homozygous B-HLA-A11.1 mice were similar to those in the C57BL/6 mice. Percent of CD8+ T cells were significantly decreased, demonstrating that introduction of hB2M-HLA-A11.1-H-2D in place of mouse B2M may affected the development of CD8 + T cells, which in turn affected the proportion of T cell subtypes in the lymph nodes. Values are expressed as mean ± SEM.
Analysis of lymph node T cell subpopulations by FACS. Lymph nodes were isolated from female C57BL/6 and B-HLA-A11.1 mice (n=3, 8-week-old). Flow cytometry analysis of the splenocytes was performed to assess leukocyte subpopulations. A. Representative FACS plots. Single live CD45+ cells were gated for TCRβ+ T cell population and used for further analysis as indicated here. B. Results of FACS analysis. The percent of Tregs in homozygous B-HLA-A11.1 mice were similar to those in the C57BL/6 mice. Percent of CD8+ T cells were significantly decreased while percent of CD4+ T cells were significantly increased, demonstrating that introduction of hB2M-HLA-A11.1-H-2D in place of mouse B2M may affected the development of CD8 + T cells, which in turn affected the proportion of T cell subtypes in the lymph nodes. Values are expressed as mean ± SEM.
Analysis of blood leukocyte subpopulations by FACS. Blood cells were isolated from female C57BL/6 and B-HLA-A11.1 mice (n=3, 8-week-old). Flow cytometry analysis of the splenocytes was performed to assess leukocyte subpopulations. A. Representative FACS plots. Single live cells were gated for the CD45+ population and used for further analysis as indicated here. B. Results of FACS analysis. Percent of total T cells, B cells, NK cells, dendritic cells, granulocytes, monocytes and macrophages in homozygous B-HLA-A11.1 mice were similar to those in the C57BL/6 mice. Percent of CD8+ T cells were significantly decreased, demonstrating that introduction of hB2M-HLA-A11.1-H-2D in place of mouse B2M may affected the development of CD8 + T cells, which in turn affected the proportion of T cell subtypes in the blood. Values are expressed as mean ± SEM.
Analysis of blood T cell subpopulations by FACS. Blood cells were isolated from female C57BL/6 and B-HLA-A11.1 mice (n=3, 8-week-old). Flow cytometry analysis of the splenocytes was performed to assess leukocyte subpopulations. A. Representative FACS plots. Single live CD45+ cells were gated for TCRβ+ T cell population and used for further analysis as indicated here. B. Results of FACS analysis. The percent of Tregs in homozygous B-HLA-A11.1 mice were similar to those in the C57BL/6 mice. Percent of CD8+ T cells were significantly decreased while percent of CD4+ T cells were significantly increased, demonstrating that introduction of hB2M-HLA-A11.1-H-2D in place of mouse B2M may affected the development of CD8 + T cells, which in turn affected the proportion of T cell subtypes in the blood. Values are expressed as mean ± SEM.
Peptide vaccines induced immune responses in B-HLA-A11.1 mice
Detection of vaccine-induced immune responses in B-HLA-A11.1 mice by IFN-γ ELISpot assay. Female C57BL/6 mice and B-HLA-A11.1 mice at the age of 7–8 weeks were divided into PBS group and KRAS peptide group (n=2), and then inoculated PBS or vaccines at the inside muscle of both legs. Three weeks after the last immunization, mice were sacrificed. The splenocytes were extracted, stimulated with individual peptide or target-unrelated polypeptide as negative control (NC) or anti-CD3 as positive control(PC), and then measured for IFN-γ secretion. No significant difference in body weight among groups (Data was not shown). (A) Representative results showing stimulation of splenocytes harvested from immunized mice with negative control, or peptide vaccines, or positive control in duplicates. (B) Summary of results. The results demonstrate that B-HLA-11.1 mice provide a powerful preclinical model for in vivo evaluation of vaccines. NC: negative control, PC: positive control.
Single-cell isolation of target peptide-specific T cells from B-HLA-A11.1 mice. B-HLA-A11.1 mice were subcutaneously immunized with the target peptide and the spleen cells from five mice displayed specific responses against the target peptide. Spleen cells from five mice (Mus-1, Mus-2, Mus-3, Mus-4 and Mus-5) that showed substantial target peptide specific responses were stained with target peptide/HLA-A*11:01 tetramer, and the tetramer positive CD8+ T cells were sorted by single-cell sorting with flow Cytometry. Mouse without target peptide immunization was enrolled as the negative control. These results demonstrated that the B-HLA-A11.1 mice could be used for identifying target peptide specific TCRs and investigating mechanisms of peptide presentation and TCR recognition of cancer targets epitopes in the context of HLA-A*11:01 (All results were provided by the client.)
Hematology analysis
Complete blood count (CBC) of B-HLA-A11.1 mice. Values are expressed as mean ± SD.
Biochemical test of B-HLA-A11.1 mice. Values are expressed as mean ± SD.
The organs of female B-HLA-A11.1 mice (8-week-old, n=10).
The organs of male B-HLA-A11.1 mice (8-week-old, n=10).
Average weight of the main organs of B-HLA-A11.1 mice. Values are expressed as mean ± SD.
Histopathological analysis of organs in B-HLA-A11.1 mice. The main organs of B-HLA-A11.1 mice were isolated at 8 weeks of age and analyzed with H&E staining (male, n=10; female, n=10). Results showed that no obvious abnormalities were found in all of the organs (brain, heart, lung, liver, spleen, stomach, small intestine, colon, kidney, ovary and testis). Scale bar: 100 μm.
010-56967680
info@bbctg.com.cn
Copyright © 2024 百奥赛图江苏基因生物技术有限公司. All Rights Reserved
备案号： 苏ICP备2021053911号-1
苏公网安备：32068402320845号
网站建设：北京分形科技
苏公网安备：32068402320845号
网站建设：北京分形科技