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MedChemExpress hy b0490 mce pe cy7 anti human cd3 cat
Hy B0490 Mce Pe Cy7 Anti Human Cd3 Cat, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Multi Sciences (Lianke) Biotech Co Ltd hy b0490 mce pe cy7 anti human cd3 cat
Hy B0490 Mce Pe Cy7 Anti Human Cd3 Cat, supplied by Multi Sciences (Lianke) Biotech Co Ltd, 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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Thermo Fisher anti-human cd3-pe cy7
Anti Human Cd3 Pe Cy7, supplied by Thermo Fisher, 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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Thermo Fisher anti-human cd3 pe/cy7
Siglec-7 ligand O-glycans suppress NK cell cytotoxity via inhibitory signal activation of ITIM/ITSM (A) The gating information for picking up NK cells from PBMCs is in <xref ref-type=Figure S5 B. The expression of Siglec-7 on NK cells from donor 1 and donor 2 was analyzed. (B) Cytotoxicity assay using co-culture of DLD-1 or ST transfectants with PBMCs. Cytotoxicity was assessed by measuring lactate dehydrogenase (LDH) activity released into the medium from injured cells. They were measured using the LDH release detection kit. E:T refers to the ratio of effector cells (PBMCs) and target cells (DLD-1 and ST transfectants). Error bars indicate SEM. ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05, using one-way ANOVA. E:T = 100:1 p = 0.0003, E:T = 50:1 p = 0.0026, E:T = 25:1 p = 0.0166, E:T = 12.5:1 p = 0.0241. Tukey’s multiple comparison test, E:T = 100:1 DLD-1 vs. C3, p = 0.0129, DLD-1 vs. C4, p = 0.0059, DLD-1 vs. C8, p = 0.0002, E:T = 50:1 DLD-1 vs. C8, p = 0.0012, E:T = 25:1 DLD-1 vs. C8, p = 0.0346, E:T = 12.5:1 DLD-1 vs. C8, p = 0.0223, E:T = 6.25:1 DLD-1 vs. C8, p = 0.0314. Data are mean ± SD, n = 7 biological replicates. (C) PBMCs were co-cultured with DLD at E:T = 100:1 after prior treatment with 10 μg/mL anti-Siglec-7 antibody or isotype control antibody. The cytotoxic activity was then assessed with the LDH release detection kit. DLD-1 Control IgG vs. DLD-1 Anti-Sig-7, p = 0.2328, C3 Control IgG vs. C3 Anti-Sig-7, p = 0.0404, C4 Control IgG vs. C4 Anti-Sig-7, p = 0.0260, C8 Control IgG vs. C8 Anti-Sig-7, p = 0.0062, Data are mean ± SD, n = 4 biological replicates. (D and E) Co-culture of an NK cell line KHYG-1-Siglec-7 high ( Figure S3 B) and DLD-1 or ST8Sia6-transfectant C8. DLD-1 and C8 were transiently transfected with a red fluoresceine protein gene for labeling of the cells. The medium contained DAPI, which stains dead cells. The magnified image in the upper right of the panel shows dead cells stained with DAPI. Dead KHYG-1-Siglec-7 high stained using DAPI are indicated with blue arrows. Time-lapse imaging of co-cultured DLD-1 or C8 and KHYG-1-Siglec-7 high was acquired for 10 h . Scale bar indicates 50 μm. (F) Assessment of NK apoptosis in PBMCs co-cultured with DLD; PBMCs were stained with anti-CD3-FITC and anti-CD16/CD56-PE after co-culturing. Further staining with Annexin-V-APC and 7-AAD comparing Annexin-V and 7-AAD co-positive populations in Gate:A (Appendix Gating Information). (G) U937-Siglec-7 high were co-cultured with DLD-1 or ST transfectants for 10 min at 37°C. The U937 cells were collected and lysed. Immunoprecipitation was performed using an anti-Siglec-7 antibody and subsequent immunoblotting with an anti-phospho-tyrosine antibody (4G10), anti-Siglec-7 antibody, or anti-SHP-1. (H) Immunoprecipitation using anti-SHP-1 antibody and subsequent IB using anti-phosphotyrosine antibody (PY20) or anti-SHP-1 were performed. Phosphorylated Siglec-7 and SHP-1 were quantitated using ImageJ software (NIH) and the ratios of p-protein/total proteins in (G) and (H) are presented in (I) and (J), respectively. (I and J) Summary of phosphorylation ratios for Siglec-7 ((I) p-Siglec-7/Siglec-7) and SHP-1 ((J) p-SHP-1/SHP-1). DLD-1 and ST transfectants vs. (A and B) PBMCs, (C) KHYG-1-Siglec-7 high and (D–F) U937-Siglec-7 high . " width="250" height="auto" />
Anti Human Cd3 Pe/Cy7, supplied by Thermo Fisher, 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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Cytek Biosciences antihuman cd3 pe cy7
Siglec-7 ligand O-glycans suppress NK cell cytotoxity via inhibitory signal activation of ITIM/ITSM (A) The gating information for picking up NK cells from PBMCs is in <xref ref-type=Figure S5 B. The expression of Siglec-7 on NK cells from donor 1 and donor 2 was analyzed. (B) Cytotoxicity assay using co-culture of DLD-1 or ST transfectants with PBMCs. Cytotoxicity was assessed by measuring lactate dehydrogenase (LDH) activity released into the medium from injured cells. They were measured using the LDH release detection kit. E:T refers to the ratio of effector cells (PBMCs) and target cells (DLD-1 and ST transfectants). Error bars indicate SEM. ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05, using one-way ANOVA. E:T = 100:1 p = 0.0003, E:T = 50:1 p = 0.0026, E:T = 25:1 p = 0.0166, E:T = 12.5:1 p = 0.0241. Tukey’s multiple comparison test, E:T = 100:1 DLD-1 vs. C3, p = 0.0129, DLD-1 vs. C4, p = 0.0059, DLD-1 vs. C8, p = 0.0002, E:T = 50:1 DLD-1 vs. C8, p = 0.0012, E:T = 25:1 DLD-1 vs. C8, p = 0.0346, E:T = 12.5:1 DLD-1 vs. C8, p = 0.0223, E:T = 6.25:1 DLD-1 vs. C8, p = 0.0314. Data are mean ± SD, n = 7 biological replicates. (C) PBMCs were co-cultured with DLD at E:T = 100:1 after prior treatment with 10 μg/mL anti-Siglec-7 antibody or isotype control antibody. The cytotoxic activity was then assessed with the LDH release detection kit. DLD-1 Control IgG vs. DLD-1 Anti-Sig-7, p = 0.2328, C3 Control IgG vs. C3 Anti-Sig-7, p = 0.0404, C4 Control IgG vs. C4 Anti-Sig-7, p = 0.0260, C8 Control IgG vs. C8 Anti-Sig-7, p = 0.0062, Data are mean ± SD, n = 4 biological replicates. (D and E) Co-culture of an NK cell line KHYG-1-Siglec-7 high ( Figure S3 B) and DLD-1 or ST8Sia6-transfectant C8. DLD-1 and C8 were transiently transfected with a red fluoresceine protein gene for labeling of the cells. The medium contained DAPI, which stains dead cells. The magnified image in the upper right of the panel shows dead cells stained with DAPI. Dead KHYG-1-Siglec-7 high stained using DAPI are indicated with blue arrows. Time-lapse imaging of co-cultured DLD-1 or C8 and KHYG-1-Siglec-7 high was acquired for 10 h . Scale bar indicates 50 μm. (F) Assessment of NK apoptosis in PBMCs co-cultured with DLD; PBMCs were stained with anti-CD3-FITC and anti-CD16/CD56-PE after co-culturing. Further staining with Annexin-V-APC and 7-AAD comparing Annexin-V and 7-AAD co-positive populations in Gate:A (Appendix Gating Information). (G) U937-Siglec-7 high were co-cultured with DLD-1 or ST transfectants for 10 min at 37°C. The U937 cells were collected and lysed. Immunoprecipitation was performed using an anti-Siglec-7 antibody and subsequent immunoblotting with an anti-phospho-tyrosine antibody (4G10), anti-Siglec-7 antibody, or anti-SHP-1. (H) Immunoprecipitation using anti-SHP-1 antibody and subsequent IB using anti-phosphotyrosine antibody (PY20) or anti-SHP-1 were performed. Phosphorylated Siglec-7 and SHP-1 were quantitated using ImageJ software (NIH) and the ratios of p-protein/total proteins in (G) and (H) are presented in (I) and (J), respectively. (I and J) Summary of phosphorylation ratios for Siglec-7 ((I) p-Siglec-7/Siglec-7) and SHP-1 ((J) p-SHP-1/SHP-1). DLD-1 and ST transfectants vs. (A and B) PBMCs, (C) KHYG-1-Siglec-7 high and (D–F) U937-Siglec-7 high . " width="250" height="auto" />
Antihuman Cd3 Pe Cy7, supplied by Cytek Biosciences, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/antihuman cd3 pe cy7/product/Cytek Biosciences
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R&D Systems vendor bcma tnfrsf17 fc alexa fluor 488 afg193 r d systems cd2 bv421 562667 bd horizon cd3 pe cy7 340948 bd biosciences cd5 percp cy5
Siglec-7 ligand O-glycans suppress NK cell cytotoxity via inhibitory signal activation of ITIM/ITSM (A) The gating information for picking up NK cells from PBMCs is in <xref ref-type=Figure S5 B. The expression of Siglec-7 on NK cells from donor 1 and donor 2 was analyzed. (B) Cytotoxicity assay using co-culture of DLD-1 or ST transfectants with PBMCs. Cytotoxicity was assessed by measuring lactate dehydrogenase (LDH) activity released into the medium from injured cells. They were measured using the LDH release detection kit. E:T refers to the ratio of effector cells (PBMCs) and target cells (DLD-1 and ST transfectants). Error bars indicate SEM. ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05, using one-way ANOVA. E:T = 100:1 p = 0.0003, E:T = 50:1 p = 0.0026, E:T = 25:1 p = 0.0166, E:T = 12.5:1 p = 0.0241. Tukey’s multiple comparison test, E:T = 100:1 DLD-1 vs. C3, p = 0.0129, DLD-1 vs. C4, p = 0.0059, DLD-1 vs. C8, p = 0.0002, E:T = 50:1 DLD-1 vs. C8, p = 0.0012, E:T = 25:1 DLD-1 vs. C8, p = 0.0346, E:T = 12.5:1 DLD-1 vs. C8, p = 0.0223, E:T = 6.25:1 DLD-1 vs. C8, p = 0.0314. Data are mean ± SD, n = 7 biological replicates. (C) PBMCs were co-cultured with DLD at E:T = 100:1 after prior treatment with 10 μg/mL anti-Siglec-7 antibody or isotype control antibody. The cytotoxic activity was then assessed with the LDH release detection kit. DLD-1 Control IgG vs. DLD-1 Anti-Sig-7, p = 0.2328, C3 Control IgG vs. C3 Anti-Sig-7, p = 0.0404, C4 Control IgG vs. C4 Anti-Sig-7, p = 0.0260, C8 Control IgG vs. C8 Anti-Sig-7, p = 0.0062, Data are mean ± SD, n = 4 biological replicates. (D and E) Co-culture of an NK cell line KHYG-1-Siglec-7 high ( Figure S3 B) and DLD-1 or ST8Sia6-transfectant C8. DLD-1 and C8 were transiently transfected with a red fluoresceine protein gene for labeling of the cells. The medium contained DAPI, which stains dead cells. The magnified image in the upper right of the panel shows dead cells stained with DAPI. Dead KHYG-1-Siglec-7 high stained using DAPI are indicated with blue arrows. Time-lapse imaging of co-cultured DLD-1 or C8 and KHYG-1-Siglec-7 high was acquired for 10 h . Scale bar indicates 50 μm. (F) Assessment of NK apoptosis in PBMCs co-cultured with DLD; PBMCs were stained with anti-CD3-FITC and anti-CD16/CD56-PE after co-culturing. Further staining with Annexin-V-APC and 7-AAD comparing Annexin-V and 7-AAD co-positive populations in Gate:A (Appendix Gating Information). (G) U937-Siglec-7 high were co-cultured with DLD-1 or ST transfectants for 10 min at 37°C. The U937 cells were collected and lysed. Immunoprecipitation was performed using an anti-Siglec-7 antibody and subsequent immunoblotting with an anti-phospho-tyrosine antibody (4G10), anti-Siglec-7 antibody, or anti-SHP-1. (H) Immunoprecipitation using anti-SHP-1 antibody and subsequent IB using anti-phosphotyrosine antibody (PY20) or anti-SHP-1 were performed. Phosphorylated Siglec-7 and SHP-1 were quantitated using ImageJ software (NIH) and the ratios of p-protein/total proteins in (G) and (H) are presented in (I) and (J), respectively. (I and J) Summary of phosphorylation ratios for Siglec-7 ((I) p-Siglec-7/Siglec-7) and SHP-1 ((J) p-SHP-1/SHP-1). DLD-1 and ST transfectants vs. (A and B) PBMCs, (C) KHYG-1-Siglec-7 high and (D–F) U937-Siglec-7 high . " width="250" height="auto" />
Vendor Bcma Tnfrsf17 Fc Alexa Fluor 488 Afg193 R D Systems Cd2 Bv421 562667 Bd Horizon Cd3 Pe Cy7 340948 Bd Biosciences Cd5 Percp Cy5, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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vendor bcma tnfrsf17 fc alexa fluor 488 afg193 r d systems cd2 bv421 562667 bd horizon cd3 pe cy7 340948 bd biosciences cd5 percp cy5 - by Bioz Stars, 2026-06
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Thermo Fisher anti-human pe/cy7-cd3 okt3
Siglec-7 ligand O-glycans suppress NK cell cytotoxity via inhibitory signal activation of ITIM/ITSM (A) The gating information for picking up NK cells from PBMCs is in <xref ref-type=Figure S5 B. The expression of Siglec-7 on NK cells from donor 1 and donor 2 was analyzed. (B) Cytotoxicity assay using co-culture of DLD-1 or ST transfectants with PBMCs. Cytotoxicity was assessed by measuring lactate dehydrogenase (LDH) activity released into the medium from injured cells. They were measured using the LDH release detection kit. E:T refers to the ratio of effector cells (PBMCs) and target cells (DLD-1 and ST transfectants). Error bars indicate SEM. ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05, using one-way ANOVA. E:T = 100:1 p = 0.0003, E:T = 50:1 p = 0.0026, E:T = 25:1 p = 0.0166, E:T = 12.5:1 p = 0.0241. Tukey’s multiple comparison test, E:T = 100:1 DLD-1 vs. C3, p = 0.0129, DLD-1 vs. C4, p = 0.0059, DLD-1 vs. C8, p = 0.0002, E:T = 50:1 DLD-1 vs. C8, p = 0.0012, E:T = 25:1 DLD-1 vs. C8, p = 0.0346, E:T = 12.5:1 DLD-1 vs. C8, p = 0.0223, E:T = 6.25:1 DLD-1 vs. C8, p = 0.0314. Data are mean ± SD, n = 7 biological replicates. (C) PBMCs were co-cultured with DLD at E:T = 100:1 after prior treatment with 10 μg/mL anti-Siglec-7 antibody or isotype control antibody. The cytotoxic activity was then assessed with the LDH release detection kit. DLD-1 Control IgG vs. DLD-1 Anti-Sig-7, p = 0.2328, C3 Control IgG vs. C3 Anti-Sig-7, p = 0.0404, C4 Control IgG vs. C4 Anti-Sig-7, p = 0.0260, C8 Control IgG vs. C8 Anti-Sig-7, p = 0.0062, Data are mean ± SD, n = 4 biological replicates. (D and E) Co-culture of an NK cell line KHYG-1-Siglec-7 high ( Figure S3 B) and DLD-1 or ST8Sia6-transfectant C8. DLD-1 and C8 were transiently transfected with a red fluoresceine protein gene for labeling of the cells. The medium contained DAPI, which stains dead cells. The magnified image in the upper right of the panel shows dead cells stained with DAPI. Dead KHYG-1-Siglec-7 high stained using DAPI are indicated with blue arrows. Time-lapse imaging of co-cultured DLD-1 or C8 and KHYG-1-Siglec-7 high was acquired for 10 h . Scale bar indicates 50 μm. (F) Assessment of NK apoptosis in PBMCs co-cultured with DLD; PBMCs were stained with anti-CD3-FITC and anti-CD16/CD56-PE after co-culturing. Further staining with Annexin-V-APC and 7-AAD comparing Annexin-V and 7-AAD co-positive populations in Gate:A (Appendix Gating Information). (G) U937-Siglec-7 high were co-cultured with DLD-1 or ST transfectants for 10 min at 37°C. The U937 cells were collected and lysed. Immunoprecipitation was performed using an anti-Siglec-7 antibody and subsequent immunoblotting with an anti-phospho-tyrosine antibody (4G10), anti-Siglec-7 antibody, or anti-SHP-1. (H) Immunoprecipitation using anti-SHP-1 antibody and subsequent IB using anti-phosphotyrosine antibody (PY20) or anti-SHP-1 were performed. Phosphorylated Siglec-7 and SHP-1 were quantitated using ImageJ software (NIH) and the ratios of p-protein/total proteins in (G) and (H) are presented in (I) and (J), respectively. (I and J) Summary of phosphorylation ratios for Siglec-7 ((I) p-Siglec-7/Siglec-7) and SHP-1 ((J) p-SHP-1/SHP-1). DLD-1 and ST transfectants vs. (A and B) PBMCs, (C) KHYG-1-Siglec-7 high and (D–F) U937-Siglec-7 high . " width="250" height="auto" />
Anti Human Pe/Cy7 Cd3 Okt3, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti-human pe/cy7-cd3 okt3/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
anti-human pe/cy7-cd3 okt3 - by Bioz Stars, 2026-06
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Thermo Fisher anti-human cd3 pe cy7
Siglec-7 ligand O-glycans suppress NK cell cytotoxity via inhibitory signal activation of ITIM/ITSM (A) The gating information for picking up NK cells from PBMCs is in <xref ref-type=Figure S5 B. The expression of Siglec-7 on NK cells from donor 1 and donor 2 was analyzed. (B) Cytotoxicity assay using co-culture of DLD-1 or ST transfectants with PBMCs. Cytotoxicity was assessed by measuring lactate dehydrogenase (LDH) activity released into the medium from injured cells. They were measured using the LDH release detection kit. E:T refers to the ratio of effector cells (PBMCs) and target cells (DLD-1 and ST transfectants). Error bars indicate SEM. ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05, using one-way ANOVA. E:T = 100:1 p = 0.0003, E:T = 50:1 p = 0.0026, E:T = 25:1 p = 0.0166, E:T = 12.5:1 p = 0.0241. Tukey’s multiple comparison test, E:T = 100:1 DLD-1 vs. C3, p = 0.0129, DLD-1 vs. C4, p = 0.0059, DLD-1 vs. C8, p = 0.0002, E:T = 50:1 DLD-1 vs. C8, p = 0.0012, E:T = 25:1 DLD-1 vs. C8, p = 0.0346, E:T = 12.5:1 DLD-1 vs. C8, p = 0.0223, E:T = 6.25:1 DLD-1 vs. C8, p = 0.0314. Data are mean ± SD, n = 7 biological replicates. (C) PBMCs were co-cultured with DLD at E:T = 100:1 after prior treatment with 10 μg/mL anti-Siglec-7 antibody or isotype control antibody. The cytotoxic activity was then assessed with the LDH release detection kit. DLD-1 Control IgG vs. DLD-1 Anti-Sig-7, p = 0.2328, C3 Control IgG vs. C3 Anti-Sig-7, p = 0.0404, C4 Control IgG vs. C4 Anti-Sig-7, p = 0.0260, C8 Control IgG vs. C8 Anti-Sig-7, p = 0.0062, Data are mean ± SD, n = 4 biological replicates. (D and E) Co-culture of an NK cell line KHYG-1-Siglec-7 high ( Figure S3 B) and DLD-1 or ST8Sia6-transfectant C8. DLD-1 and C8 were transiently transfected with a red fluoresceine protein gene for labeling of the cells. The medium contained DAPI, which stains dead cells. The magnified image in the upper right of the panel shows dead cells stained with DAPI. Dead KHYG-1-Siglec-7 high stained using DAPI are indicated with blue arrows. Time-lapse imaging of co-cultured DLD-1 or C8 and KHYG-1-Siglec-7 high was acquired for 10 h . Scale bar indicates 50 μm. (F) Assessment of NK apoptosis in PBMCs co-cultured with DLD; PBMCs were stained with anti-CD3-FITC and anti-CD16/CD56-PE after co-culturing. Further staining with Annexin-V-APC and 7-AAD comparing Annexin-V and 7-AAD co-positive populations in Gate:A (Appendix Gating Information). (G) U937-Siglec-7 high were co-cultured with DLD-1 or ST transfectants for 10 min at 37°C. The U937 cells were collected and lysed. Immunoprecipitation was performed using an anti-Siglec-7 antibody and subsequent immunoblotting with an anti-phospho-tyrosine antibody (4G10), anti-Siglec-7 antibody, or anti-SHP-1. (H) Immunoprecipitation using anti-SHP-1 antibody and subsequent IB using anti-phosphotyrosine antibody (PY20) or anti-SHP-1 were performed. Phosphorylated Siglec-7 and SHP-1 were quantitated using ImageJ software (NIH) and the ratios of p-protein/total proteins in (G) and (H) are presented in (I) and (J), respectively. (I and J) Summary of phosphorylation ratios for Siglec-7 ((I) p-Siglec-7/Siglec-7) and SHP-1 ((J) p-SHP-1/SHP-1). DLD-1 and ST transfectants vs. (A and B) PBMCs, (C) KHYG-1-Siglec-7 high and (D–F) U937-Siglec-7 high . " width="250" height="auto" />
Anti Human Cd3 Pe Cy7, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti-human cd3 pe cy7/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
anti-human cd3 pe cy7 - by Bioz Stars, 2026-06
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90
Becton Dickinson pe-cy7 mouse anti-human cd3
Siglec-7 ligand O-glycans suppress NK cell cytotoxity via inhibitory signal activation of ITIM/ITSM (A) The gating information for picking up NK cells from PBMCs is in <xref ref-type=Figure S5 B. The expression of Siglec-7 on NK cells from donor 1 and donor 2 was analyzed. (B) Cytotoxicity assay using co-culture of DLD-1 or ST transfectants with PBMCs. Cytotoxicity was assessed by measuring lactate dehydrogenase (LDH) activity released into the medium from injured cells. They were measured using the LDH release detection kit. E:T refers to the ratio of effector cells (PBMCs) and target cells (DLD-1 and ST transfectants). Error bars indicate SEM. ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05, using one-way ANOVA. E:T = 100:1 p = 0.0003, E:T = 50:1 p = 0.0026, E:T = 25:1 p = 0.0166, E:T = 12.5:1 p = 0.0241. Tukey’s multiple comparison test, E:T = 100:1 DLD-1 vs. C3, p = 0.0129, DLD-1 vs. C4, p = 0.0059, DLD-1 vs. C8, p = 0.0002, E:T = 50:1 DLD-1 vs. C8, p = 0.0012, E:T = 25:1 DLD-1 vs. C8, p = 0.0346, E:T = 12.5:1 DLD-1 vs. C8, p = 0.0223, E:T = 6.25:1 DLD-1 vs. C8, p = 0.0314. Data are mean ± SD, n = 7 biological replicates. (C) PBMCs were co-cultured with DLD at E:T = 100:1 after prior treatment with 10 μg/mL anti-Siglec-7 antibody or isotype control antibody. The cytotoxic activity was then assessed with the LDH release detection kit. DLD-1 Control IgG vs. DLD-1 Anti-Sig-7, p = 0.2328, C3 Control IgG vs. C3 Anti-Sig-7, p = 0.0404, C4 Control IgG vs. C4 Anti-Sig-7, p = 0.0260, C8 Control IgG vs. C8 Anti-Sig-7, p = 0.0062, Data are mean ± SD, n = 4 biological replicates. (D and E) Co-culture of an NK cell line KHYG-1-Siglec-7 high ( Figure S3 B) and DLD-1 or ST8Sia6-transfectant C8. DLD-1 and C8 were transiently transfected with a red fluoresceine protein gene for labeling of the cells. The medium contained DAPI, which stains dead cells. The magnified image in the upper right of the panel shows dead cells stained with DAPI. Dead KHYG-1-Siglec-7 high stained using DAPI are indicated with blue arrows. Time-lapse imaging of co-cultured DLD-1 or C8 and KHYG-1-Siglec-7 high was acquired for 10 h . Scale bar indicates 50 μm. (F) Assessment of NK apoptosis in PBMCs co-cultured with DLD; PBMCs were stained with anti-CD3-FITC and anti-CD16/CD56-PE after co-culturing. Further staining with Annexin-V-APC and 7-AAD comparing Annexin-V and 7-AAD co-positive populations in Gate:A (Appendix Gating Information). (G) U937-Siglec-7 high were co-cultured with DLD-1 or ST transfectants for 10 min at 37°C. The U937 cells were collected and lysed. Immunoprecipitation was performed using an anti-Siglec-7 antibody and subsequent immunoblotting with an anti-phospho-tyrosine antibody (4G10), anti-Siglec-7 antibody, or anti-SHP-1. (H) Immunoprecipitation using anti-SHP-1 antibody and subsequent IB using anti-phosphotyrosine antibody (PY20) or anti-SHP-1 were performed. Phosphorylated Siglec-7 and SHP-1 were quantitated using ImageJ software (NIH) and the ratios of p-protein/total proteins in (G) and (H) are presented in (I) and (J), respectively. (I and J) Summary of phosphorylation ratios for Siglec-7 ((I) p-Siglec-7/Siglec-7) and SHP-1 ((J) p-SHP-1/SHP-1). DLD-1 and ST transfectants vs. (A and B) PBMCs, (C) KHYG-1-Siglec-7 high and (D–F) U937-Siglec-7 high . " width="250" height="auto" />
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Siglec-7 ligand O-glycans suppress NK cell cytotoxity via inhibitory signal activation of ITIM/ITSM (A) The gating information for picking up NK cells from PBMCs is in <xref ref-type=Figure S5 B. The expression of Siglec-7 on NK cells from donor 1 and donor 2 was analyzed. (B) Cytotoxicity assay using co-culture of DLD-1 or ST transfectants with PBMCs. Cytotoxicity was assessed by measuring lactate dehydrogenase (LDH) activity released into the medium from injured cells. They were measured using the LDH release detection kit. E:T refers to the ratio of effector cells (PBMCs) and target cells (DLD-1 and ST transfectants). Error bars indicate SEM. ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05, using one-way ANOVA. E:T = 100:1 p = 0.0003, E:T = 50:1 p = 0.0026, E:T = 25:1 p = 0.0166, E:T = 12.5:1 p = 0.0241. Tukey’s multiple comparison test, E:T = 100:1 DLD-1 vs. C3, p = 0.0129, DLD-1 vs. C4, p = 0.0059, DLD-1 vs. C8, p = 0.0002, E:T = 50:1 DLD-1 vs. C8, p = 0.0012, E:T = 25:1 DLD-1 vs. C8, p = 0.0346, E:T = 12.5:1 DLD-1 vs. C8, p = 0.0223, E:T = 6.25:1 DLD-1 vs. C8, p = 0.0314. Data are mean ± SD, n = 7 biological replicates. (C) PBMCs were co-cultured with DLD at E:T = 100:1 after prior treatment with 10 μg/mL anti-Siglec-7 antibody or isotype control antibody. The cytotoxic activity was then assessed with the LDH release detection kit. DLD-1 Control IgG vs. DLD-1 Anti-Sig-7, p = 0.2328, C3 Control IgG vs. C3 Anti-Sig-7, p = 0.0404, C4 Control IgG vs. C4 Anti-Sig-7, p = 0.0260, C8 Control IgG vs. C8 Anti-Sig-7, p = 0.0062, Data are mean ± SD, n = 4 biological replicates. (D and E) Co-culture of an NK cell line KHYG-1-Siglec-7 high ( Figure S3 B) and DLD-1 or ST8Sia6-transfectant C8. DLD-1 and C8 were transiently transfected with a red fluoresceine protein gene for labeling of the cells. The medium contained DAPI, which stains dead cells. The magnified image in the upper right of the panel shows dead cells stained with DAPI. Dead KHYG-1-Siglec-7 high stained using DAPI are indicated with blue arrows. Time-lapse imaging of co-cultured DLD-1 or C8 and KHYG-1-Siglec-7 high was acquired for 10 h . Scale bar indicates 50 μm. (F) Assessment of NK apoptosis in PBMCs co-cultured with DLD; PBMCs were stained with anti-CD3-FITC and anti-CD16/CD56-PE after co-culturing. Further staining with Annexin-V-APC and 7-AAD comparing Annexin-V and 7-AAD co-positive populations in Gate:A (Appendix Gating Information). (G) U937-Siglec-7 high were co-cultured with DLD-1 or ST transfectants for 10 min at 37°C. The U937 cells were collected and lysed. Immunoprecipitation was performed using an anti-Siglec-7 antibody and subsequent immunoblotting with an anti-phospho-tyrosine antibody (4G10), anti-Siglec-7 antibody, or anti-SHP-1. (H) Immunoprecipitation using anti-SHP-1 antibody and subsequent IB using anti-phosphotyrosine antibody (PY20) or anti-SHP-1 were performed. Phosphorylated Siglec-7 and SHP-1 were quantitated using ImageJ software (NIH) and the ratios of p-protein/total proteins in (G) and (H) are presented in (I) and (J), respectively. (I and J) Summary of phosphorylation ratios for Siglec-7 ((I) p-Siglec-7/Siglec-7) and SHP-1 ((J) p-SHP-1/SHP-1). DLD-1 and ST transfectants vs. (A and B) PBMCs, (C) KHYG-1-Siglec-7 high and (D–F) U937-Siglec-7 high . " width="100%" height="100%">

Journal: iScience

Article Title: Bidirectional signals generated by Siglec-7 and its crucial ligand tri-sialylated T to escape of cancer cells from immune surveillance

doi: 10.1016/j.isci.2024.111139

Figure Lengend Snippet: Siglec-7 ligand O-glycans suppress NK cell cytotoxity via inhibitory signal activation of ITIM/ITSM (A) The gating information for picking up NK cells from PBMCs is in Figure S5 B. The expression of Siglec-7 on NK cells from donor 1 and donor 2 was analyzed. (B) Cytotoxicity assay using co-culture of DLD-1 or ST transfectants with PBMCs. Cytotoxicity was assessed by measuring lactate dehydrogenase (LDH) activity released into the medium from injured cells. They were measured using the LDH release detection kit. E:T refers to the ratio of effector cells (PBMCs) and target cells (DLD-1 and ST transfectants). Error bars indicate SEM. ∗∗∗ p < 0.001, ∗∗ p < 0.01, ∗ p < 0.05, using one-way ANOVA. E:T = 100:1 p = 0.0003, E:T = 50:1 p = 0.0026, E:T = 25:1 p = 0.0166, E:T = 12.5:1 p = 0.0241. Tukey’s multiple comparison test, E:T = 100:1 DLD-1 vs. C3, p = 0.0129, DLD-1 vs. C4, p = 0.0059, DLD-1 vs. C8, p = 0.0002, E:T = 50:1 DLD-1 vs. C8, p = 0.0012, E:T = 25:1 DLD-1 vs. C8, p = 0.0346, E:T = 12.5:1 DLD-1 vs. C8, p = 0.0223, E:T = 6.25:1 DLD-1 vs. C8, p = 0.0314. Data are mean ± SD, n = 7 biological replicates. (C) PBMCs were co-cultured with DLD at E:T = 100:1 after prior treatment with 10 μg/mL anti-Siglec-7 antibody or isotype control antibody. The cytotoxic activity was then assessed with the LDH release detection kit. DLD-1 Control IgG vs. DLD-1 Anti-Sig-7, p = 0.2328, C3 Control IgG vs. C3 Anti-Sig-7, p = 0.0404, C4 Control IgG vs. C4 Anti-Sig-7, p = 0.0260, C8 Control IgG vs. C8 Anti-Sig-7, p = 0.0062, Data are mean ± SD, n = 4 biological replicates. (D and E) Co-culture of an NK cell line KHYG-1-Siglec-7 high ( Figure S3 B) and DLD-1 or ST8Sia6-transfectant C8. DLD-1 and C8 were transiently transfected with a red fluoresceine protein gene for labeling of the cells. The medium contained DAPI, which stains dead cells. The magnified image in the upper right of the panel shows dead cells stained with DAPI. Dead KHYG-1-Siglec-7 high stained using DAPI are indicated with blue arrows. Time-lapse imaging of co-cultured DLD-1 or C8 and KHYG-1-Siglec-7 high was acquired for 10 h . Scale bar indicates 50 μm. (F) Assessment of NK apoptosis in PBMCs co-cultured with DLD; PBMCs were stained with anti-CD3-FITC and anti-CD16/CD56-PE after co-culturing. Further staining with Annexin-V-APC and 7-AAD comparing Annexin-V and 7-AAD co-positive populations in Gate:A (Appendix Gating Information). (G) U937-Siglec-7 high were co-cultured with DLD-1 or ST transfectants for 10 min at 37°C. The U937 cells were collected and lysed. Immunoprecipitation was performed using an anti-Siglec-7 antibody and subsequent immunoblotting with an anti-phospho-tyrosine antibody (4G10), anti-Siglec-7 antibody, or anti-SHP-1. (H) Immunoprecipitation using anti-SHP-1 antibody and subsequent IB using anti-phosphotyrosine antibody (PY20) or anti-SHP-1 were performed. Phosphorylated Siglec-7 and SHP-1 were quantitated using ImageJ software (NIH) and the ratios of p-protein/total proteins in (G) and (H) are presented in (I) and (J), respectively. (I and J) Summary of phosphorylation ratios for Siglec-7 ((I) p-Siglec-7/Siglec-7) and SHP-1 ((J) p-SHP-1/SHP-1). DLD-1 and ST transfectants vs. (A and B) PBMCs, (C) KHYG-1-Siglec-7 high and (D–F) U937-Siglec-7 high .

Article Snippet: Anti-human CD3 PE/Cy7 , Thermo Fisher Scientific , Cat# 25-0037-42, RRID: AB_2573326.

Techniques: Activation Assay, Expressing, Cytotoxicity Assay, Co-Culture Assay, Activity Assay, Comparison, Cell Culture, Control, Transfection, Labeling, Staining, Imaging, Immunoprecipitation, Western Blot, Software, Phospho-proteomics

Journal: iScience

Article Title: Bidirectional signals generated by Siglec-7 and its crucial ligand tri-sialylated T to escape of cancer cells from immune surveillance

doi: 10.1016/j.isci.2024.111139

Figure Lengend Snippet:

Article Snippet: Anti-human CD3 PE/Cy7 , Thermo Fisher Scientific , Cat# 25-0037-42, RRID: AB_2573326.

Techniques: Blocking Assay, Plasmid Preparation, Purification, Control, Staining, Recombinant, Membrane, Mutagenesis, Cytotoxicity Assay, Cloning, Expressing, Sequencing, Software