Strain Name |
C57BL/6N-Pdcd1tm1(EGFP)Bcgen/Bcgen
|
Stock No. | 110166 |
Common name |
B-PD-1-EGFP KI mice |
Background | C57BL/6N |
Aliases | CD279, PD-1, PD1, SLEB2, hPD-1, hPD1, Hsle1, EGFP | ||
NCBI Gene ID |
18566 |
Application
• Validation of the function of PD-1 in the development of tumor and autoimmune disease
• Trace the functional cells in the development of tumor and autoimmune disease by the expression of EGFP
Targeting Stategy
Gene targeting strategy for B-PD-1-EGFP
KI mice. The EGFP gene encoding green
fluorescent protein was inserted after the 5 'UTR sequences of mouse PD-1 gene
to replace it in B-PD-1-EGFP mice.
Strain specific PD-1 and EGFP expression
analysis in heterozygous and homozygous B-PD-1-EGFP KI mice by flow cytometry. Splenocytes were collected from WT (+/+), heterozygous (H/+) and
homozygous (H/H) B-PD-1-EGFP KI mice and analyzed by flow cytometry with
species-specific anti-PD1 and anti-EGFP antibodies. Mouse PD-1 was detectable
in WT and heterozygous B-PD-1-EGFP KI mice. EGFP was detectable in heterozygous
and homozygous B-PD-1-EGFP KI mice but not in WT mice.
Analysis of Spleen Leukocytes Cell Subpopulations in B-PD-1-EGFP KI Mice
Analysis of spleen leukocyte
subpopulations by FACS. Splenocytes were isolated from female C57BL/6
and B-PD-1-EGFP KI mice (n=3, 7-week-old). Flow cytometry analysis of the splenocytes
was performed to assess leukocyte subpopulations. A. Representative FACS plots.
Single live cells were gated for CD45 population and used for further analysis
as indicated here. B. Results of FACS analysis. Percent of T cells, B cells in
B-PD-1-EGFP KI mice were higher than those in the C57BL/6 mice. While NK cells,
DCs, granulocytes, monocytes and macrophages in B-PD-1-EGFP KI mice were
similar to those in the C57BL/6 mice, demonstrating that Knock out of Mpd-1 may
change the development, differentiation or distribution of some cell types in
spleen. Values are expressed as mean ± SEM.
Analysis of Spleen T Cell Subpopulations in B-PD-1-EGFP KI Mice
Analysis of spleen T cell subpopulations by FACS. Splenocytes were isolated from female C57BL/6 and B-PD-1-EGFP KI mice (n=3, 7-week-old). Flow cytometry analysis of the splenocytes was performed to assess leukocyte subpopulations. A. Representative FACS plots. Single live CD45+ T cells were gated for CD3+ T cell population and used for further analysis as indicated here. B. Results of FACS analysis. Percent of CD8+ T cells, CD4+ T cells in B-PD-1-EGFP KI mice were similar to those in the C57BL/6 mice, while percent of Tregs in homozygous B-PD-1-EGFP KI mice were higher than those in the C57BL/6 mice, demonstrating that knock out of PD-1 may changed the development, differentiation or distribution of these Tregs in spleen. Values are expressed as mean ± SEM.