negative mouse cd8 tcell Search Results


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Miltenyi Biotec mouse cd8 tcell purification kit miltenyi biotech
Mouse Cd8 Tcell Purification Kit Miltenyi Biotech, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Easysep Mouse Naive Cd8 Tcell Isolation Kits, supplied by STEMCELL Technologies Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of <t>CD8þ</t> T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.
Themagcellect Human Cd8þ Tcell Isolation Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Miltenyi Biotec negative mouse cd8 tcell
Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of <t>CD8þ</t> T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.
Negative Mouse Cd8 Tcell, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of <t>CD8þ</t> T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.
Anti Mouse Cd8 Magnetic Particles Dm, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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NSJ Bioreagents cd4 antibody
Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of <t>CD8þ</t> T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.
Cd4 Antibody, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio X Cell anti cd8 mab
Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of <t>CD8þ</t> T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.
Anti Cd8 Mab, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Broad Institute Inc msigdb c2
Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of <t>CD8þ</t> T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.
Msigdb C2, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of <t>CD8þ</t> T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.
Magnetic Beads, supplied by STEMCELL Technologies Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson imag cell separation magnet
Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of <t>CD8þ</t> T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.
Imag Cell Separation Magnet, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of <t>CD8þ</t> T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.
Rat Anti Pig Apc, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of <t>CD8þ</t> T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.
Mouse Monoclonal Antibodies Conjugated With Fluorescein Isothiocyanate And Phycoerythrin Cd3/Cd4, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.

Journal: Cancer Research

Article Title: FGFR3 Destabilizes PD-L1 via NEDD4 to Control T-cell–Mediated Bladder Cancer Immune Surveillance

doi: 10.1158/0008-5472.can-21-2362

Figure Lengend Snippet: Figure 1. Erdafitinib and infigratinib inhibit bladder tumor growth and induce T-cell suppression accompanied with PD-L1 upregulation in mice. A and B, The overview of experimental plan in Luciþ MB49 tumor-bearing C57BL/6 (A) and nude (B) mice model. C and D, Bioluminescence images of Luciþ MB49 tumor-bearing mice model in different groups. E and F, Quantification of bioluminescence intensity (mean SD, n ¼ 5). G and H, Macroscopic images of excised bladder tumors. Scale bars, 1 cm. I and J, Tumor weight after erdafitinib and infigratinib treatment (mean SD, n ¼ 5). K and L, Ultrasound images of orthotopic bladder tumors (red dash lines), hematoxylin and eosin (H&E)–stained sections of tumors, and immunofluorescence images of the indicated markers for Ki67 (red), cytokine 7 (green), and DAPI (blue) in C57BL/6 and nude mice. Scale bars in ultrasound images, 2 mm, 500 mm for hematoxylin and eosin staining, and 20 mm for immunofluorescence images. M, PD-L1 t-SNE plots of gated flow cytometrydata generated bycells in tumor tissue from erdafitinib and infigratinib treatment. Numbers on the right edge represent the proportion of PD-L1 positive cells. N, Plot showing the proportion of PD-L1 positive cells (mean SD, n ¼ 3). O, Intratumoral CD3þCD8þ T-cell proportions were analyzed by flow cytometry. P, Plot showing the proportion of tumor-infiltrating CD3þCD8þ T cells in tumor-bearing mice with different treatment (mean SD, n ¼ 3). Q, Flow cytometry analysis showing the granzyme B–positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). R, Statistical diagram showing the granzyme B–positive ratio in CD8þ T cells (left) and granzyme Bþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). S, Flow cytometry analysis showing the TNFa-positive ratio of CD8þ T cells in tumor (mean SD, n ¼ 3). T, Statistical diagram showing the TNFa-positive ratio of CD3þCD8þ T cells (left) and TNFaþ CD8þ T cells (right) in tumor (mean SD, n ¼ 3). , P < 0.01; , P < 0.001; , P < 0.0001; one-way ANOVA.

Article Snippet: Enrichment of CD8þT cells was performed bymagnetic cell sorting (MACS) using theMagCellect Human CD8þ TCell Isolation Kit (R&D Systems) and MagCellect Mouse CD8þ T Cell Isolation Kit (R&D Systems) following the manufacturer’s instructions.

Techniques: Staining, Generated, Cytometry, Flow Cytometry