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Proteintech ras related c3 botulinum toxin substrate 2 rac2
Ras Related C3 Botulinum Toxin Substrate 2 Rac2, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 29 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+rac2+antibody/RAC2+Antibody/pm41912523-227-22-36
Average 94 stars, based on 29 article reviews

ras related c3 botulinum toxin substrate 2 rac2 - by Bioz Stars, 2026-10

94/100 stars

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Centrifugation:

Article Title: SIRT5–RAC2 Axis Drives Monocyte‐to‐Macrophage Differentiation to Promote Inflammatory Injury in Premature Ovarian Insufficiency
Article Snippet: .. Lysates were clarified by centrifugation at 8000 × g for 10 min at 4°C, and the supernatants were incubated overnight at 4°C with 10 μg of anti‐RAC2 antibody (Proteintech, China) or normal mouse IgG (Proteintech, China) as a negative control. .. Immune complexes were captured using Protein A/G magnetic beads (Vazyme, China) for 2 h at 4°C, followed by three washes with RIPA buffer.

Article Title: SIRT5-RAC2 Axis Drives Monocyte-to-Macrophage Differentiation to Promote Inflammatory Injury in Premature Ovarian Insufficiency.
Article Snippet: .. Lysates were clarified by centrifugation at 8000 × g for 10 min at 4◦C, and the supernatants were incubated overnight at 4◦C with 10 μg of anti-RAC2 antibody (Proteintech, China) or normal mouse IgG (Proteintech, China) as a negative control. .. Immune complexes were captured using Protein A/G magnetic beads (Vazyme, China) for 2 h at 4◦C, followed by three washes with RIPA buffer.

Incubation:

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Efferocytosis and polarization of macrophages were analyzed in vitro (A) Western blotting verifies the differences in TP63 and RAC2 protein expression levels in the shTP63 and shTP63+RAC2 groups compared with the control group. (B) Differences in the fluorescence signal intensity of CMFDA green among groups of human primary macrophages with EC9706. ∗ p < 0.05. (C) Differences in the fluorescence signal intensity of CMFDA green among groups in THP-1-induced macrophages with EC9706. ∗∗ p < 0.01. (D) The fluorescence signal intensity of CMFDA green in human primary macrophages treated with EC9706 was determined by flow cytometry. ∗∗∗ p < 0.001. (E) The fluorescence signal intensity of CMFDA green in THP-1-induced macrophages treated with EC9706 was determined by flow cytometry. ∗∗∗ p < 0.001. (F) The CD163 + cell level of each group in human primary macrophages with EC9706. ∗∗ p < 0.01, ∗∗∗ p < 0.001. (G) The CD163 + cell level of each group in THP-1-induced macrophages with EC9706. ∗∗∗ p < 0.001. (H) The CD86 + cells in each group of human primary macrophages treated with EC9706. ∗∗ p < 0.01, ∗∗∗ p < 0.001. (I) The CD86 + cells in each group of THP-1-induced macrophages treated with EC9706. ∗∗∗ p < 0.001. (J) Differences in IL-10, TGF-β, and TNF-α levels among the groups in human primary macrophages with EC9706. ∗∗∗ p < 0.001. (K) Differences in IL-10, TGF-β, and TNF-α levels among the groups in THP-1-induced macrophages with EC9706. Data are presented as the mean ± SD of five independent experiments. ∗∗∗ p < 0.001.

Journal: Cell Reports Medicine

Article Title: Macrophage efferocytosis mediated by the TP63-RAC2 pathway promotes immunosuppressive remodeling in esophageal cancer

doi: 10.1016/j.xcrm.2025.102529

Figure Lengend Snippet: Efferocytosis and polarization of macrophages were analyzed in vitro (A) Western blotting verifies the differences in TP63 and RAC2 protein expression levels in the shTP63 and shTP63+RAC2 groups compared with the control group. (B) Differences in the fluorescence signal intensity of CMFDA green among groups of human primary macrophages with EC9706. ∗ p < 0.05. (C) Differences in the fluorescence signal intensity of CMFDA green among groups in THP-1-induced macrophages with EC9706. ∗∗ p < 0.01. (D) The fluorescence signal intensity of CMFDA green in human primary macrophages treated with EC9706 was determined by flow cytometry. ∗∗∗ p < 0.001. (E) The fluorescence signal intensity of CMFDA green in THP-1-induced macrophages treated with EC9706 was determined by flow cytometry. ∗∗∗ p < 0.001. (F) The CD163 + cell level of each group in human primary macrophages with EC9706. ∗∗ p < 0.01, ∗∗∗ p < 0.001. (G) The CD163 + cell level of each group in THP-1-induced macrophages with EC9706. ∗∗∗ p < 0.001. (H) The CD86 + cells in each group of human primary macrophages treated with EC9706. ∗∗ p < 0.01, ∗∗∗ p < 0.001. (I) The CD86 + cells in each group of THP-1-induced macrophages treated with EC9706. ∗∗∗ p < 0.001. (J) Differences in IL-10, TGF-β, and TNF-α levels among the groups in human primary macrophages with EC9706. ∗∗∗ p < 0.001. (K) Differences in IL-10, TGF-β, and TNF-α levels among the groups in THP-1-induced macrophages with EC9706. Data are presented as the mean ± SD of five independent experiments. ∗∗∗ p < 0.001.

Article Snippet: Then, slides were treated by microwave to induce antigen retrieval using citric acid solution for 15 min. For mIHC analysis of human samples, a panel of primary antibodies were used, including CD68 (1:100, ab283654, Abcam), Annexin A1 (1:1000, ab214486, Abcam), TP63(1:200, ab124762, Abcam), RAC2(1:2000,60077-1-Ig, Proteintech).

Techniques: In Vitro, Western Blot, Expressing, Control, Fluorescence, Flow Cytometry

Experimental study of shTP63 and shTP63+RAC2 in apoptotic AKR (apoptotic esophageal carcinoma) cells-C57BL/6 efferocytosis mouse model (A) Western blot verifies the difference in TP63 and RAC2 protein expression levels in shTP63 and shTP63+RAC2 groups compared with the control group. (B) The efferocytosis index level of each group was detected ( n = 5 per group). ∗∗ p < 0.01, ∗∗∗ p < 0.001. (C) The CD163 + cells in each group were detected ( n = 5 per group). ∗ p < 0.05, ∗∗ p < 0.01. (D) The CD86 + cells in each group ( n = 5 per group). ∗∗ p < 0.01, ∗∗∗ p < 0.001.

Journal: Cell Reports Medicine

Article Title: Macrophage efferocytosis mediated by the TP63-RAC2 pathway promotes immunosuppressive remodeling in esophageal cancer

doi: 10.1016/j.xcrm.2025.102529

Figure Lengend Snippet: Experimental study of shTP63 and shTP63+RAC2 in apoptotic AKR (apoptotic esophageal carcinoma) cells-C57BL/6 efferocytosis mouse model (A) Western blot verifies the difference in TP63 and RAC2 protein expression levels in shTP63 and shTP63+RAC2 groups compared with the control group. (B) The efferocytosis index level of each group was detected ( n = 5 per group). ∗∗ p < 0.01, ∗∗∗ p < 0.001. (C) The CD163 + cells in each group were detected ( n = 5 per group). ∗ p < 0.05, ∗∗ p < 0.01. (D) The CD86 + cells in each group ( n = 5 per group). ∗∗ p < 0.01, ∗∗∗ p < 0.001.

Techniques: Western Blot, Expressing, Control

Figure 1 NK killing stress induces high expression of RAC2 in tumor cells. (A) Pathway enrichment analysis on RNA sequencing result from NK killing resistance genes. (B) A schematic diagram illustrating the flow cytometry sorting procedure employed for the identification of NK cell resistance genes within the Rho GTPase family. (C) A schematic diagram illustrating 16 genes from five subfamilies of the Rho GTPase family. (D–E) q-PCR was used to detect the expression levels of CDC42 (D) and RAC2 (E) in HeLa cells following co-culture with NK-92MI cells. The P-sup group refers to the supernatant from PBMCs that were stimulated with anti-human CD3/CD28 monoclonal antibodies for 2 days. HeLa cells cultured with this supernatant served as a positive control. The HeLa-ctrl group was used as a control to account for any stress induced by the flow cytometry sorting process; this group consisted of HeLa cells individually cultured under the same flow cytometry sorting conditions as the experimental group. (F–G) HeLa cells treated with RAC1, RAC2, RAC3, RHOG, and CDC42 gene-specific siRNAs were used to detect cell death rate by FACS following co-culture with NK-92MI cells at 6 hours. The results are representative of at least three independent experiments. Vertical bars indicate mean±SEM. Statistical significance between groups was assessed using the one-way analysis of variance with Bonferroni’s post-test, *p<0.05; **p<0.01; ***p<0.001. ctrl, control; E:T, effector-to-target; CFSE, Carboxyfluorescein succinimidyl ester; FACS, fluorescence-activated cell sorting; h, hours; NK, natural killer; PBMCs, peripheral blood mononuclear cells; q-PCR, quantitative PCR; Rho, Ras homology; RFU, relative fluorescence units; siRNA, small interfering RNA.

Journal: Journal for immunotherapy of cancer

Article Title: RAC2 inhibition enhances tumor sensitivity to NK cell-mediated cytotoxicity.

doi: 10.1136/jitc-2024-010931

Figure Lengend Snippet: Figure 1 NK killing stress induces high expression of RAC2 in tumor cells. (A) Pathway enrichment analysis on RNA sequencing result from NK killing resistance genes. (B) A schematic diagram illustrating the flow cytometry sorting procedure employed for the identification of NK cell resistance genes within the Rho GTPase family. (C) A schematic diagram illustrating 16 genes from five subfamilies of the Rho GTPase family. (D–E) q-PCR was used to detect the expression levels of CDC42 (D) and RAC2 (E) in HeLa cells following co-culture with NK-92MI cells. The P-sup group refers to the supernatant from PBMCs that were stimulated with anti-human CD3/CD28 monoclonal antibodies for 2 days. HeLa cells cultured with this supernatant served as a positive control. The HeLa-ctrl group was used as a control to account for any stress induced by the flow cytometry sorting process; this group consisted of HeLa cells individually cultured under the same flow cytometry sorting conditions as the experimental group. (F–G) HeLa cells treated with RAC1, RAC2, RAC3, RHOG, and CDC42 gene-specific siRNAs were used to detect cell death rate by FACS following co-culture with NK-92MI cells at 6 hours. The results are representative of at least three independent experiments. Vertical bars indicate mean±SEM. Statistical significance between groups was assessed using the one-way analysis of variance with Bonferroni’s post-test, *p<0.05; **p<0.01; ***p<0.001. ctrl, control; E:T, effector-to-target; CFSE, Carboxyfluorescein succinimidyl ester; FACS, fluorescence-activated cell sorting; h, hours; NK, natural killer; PBMCs, peripheral blood mononuclear cells; q-PCR, quantitative PCR; Rho, Ras homology; RFU, relative fluorescence units; siRNA, small interfering RNA.

Article Snippet: The antibodies used for Western blot analysis included Anti- RAC2 (Santa Cruz Biotechnology, sc- 517424), AntiFlag- HRP (Sigma- Aldrich, sc- F1804), and anti-β-ACTIN (Santa Cruz Biotechnology, sc- 47778).

Techniques: Expressing, RNA Sequencing, Flow Cytometry, Co-Culture Assay, Bioprocessing, Cell Culture, Positive Control, Control, Fluorescence, FACS, Real-time Polymerase Chain Reaction, Small Interfering RNA

Figure 2 RAC2 expression in tumor cells promotes tumor resistance to NK cytotoxicity. (A) Western blot and q-PCR were used to assess the efficiency of RAC2 knockout or knockdown in HeLa-sgRAC2 and HeLa-shRAC2 cell lines. (B) NK-92MI cells were co-cultured with Hela, Hela-sgRAC2, and Hela-shRAC2 cells, while the K562 co-culture group served as the positive control. The rate of tumor cell death following co-culture was assessed by FACS. (C) HeLa WT and HeLa-sgRAC2 cells, were co- cultured with primary human NK cells, and the rate of tumor cell death following co-culture was assessed by FACS. (D) Western blot and q-PCR were used to verify the knockout or knockdown efficiency of Rac2 in EL4-sgRac2 and EL4-shRac2 cell lines. (E) EL4, EL4-sgRac2, EL4-shRac2 cells were co-cultured with primary mouse NK cells, and the rate of tumor cell death after co-culture was assessed using FACS, with the EL4-shβ2m co-culture group serving as the positive control. (F) Western blot was used to verify the inhibition efficiency of RAC2 in EL4 cells following treatment with EHT-1864. Additionally, the cell death rate in tumor cells was evaluated using FACS after co-culture with primary mouse NK cells. The results are representative of at least three independent experiments. Vertical bars indicate mean±SEM. Statistical significance between groups was assessed using the one-way analysis of variance with Bonferroni’s post-test, *p<0.05; **p<0.01; ***p<0.001. CFSE, Carboxyfluorescein succinimidyl ester; E:T, effector-to-target; FACS, fluorescence-activated cell sorting; h, hours; NK, natural killer; q-PCR, quantitative PCR; WT, wild type.

Journal: Journal for immunotherapy of cancer

Article Title: RAC2 inhibition enhances tumor sensitivity to NK cell-mediated cytotoxicity.

doi: 10.1136/jitc-2024-010931

Figure Lengend Snippet: Figure 2 RAC2 expression in tumor cells promotes tumor resistance to NK cytotoxicity. (A) Western blot and q-PCR were used to assess the efficiency of RAC2 knockout or knockdown in HeLa-sgRAC2 and HeLa-shRAC2 cell lines. (B) NK-92MI cells were co-cultured with Hela, Hela-sgRAC2, and Hela-shRAC2 cells, while the K562 co-culture group served as the positive control. The rate of tumor cell death following co-culture was assessed by FACS. (C) HeLa WT and HeLa-sgRAC2 cells, were co- cultured with primary human NK cells, and the rate of tumor cell death following co-culture was assessed by FACS. (D) Western blot and q-PCR were used to verify the knockout or knockdown efficiency of Rac2 in EL4-sgRac2 and EL4-shRac2 cell lines. (E) EL4, EL4-sgRac2, EL4-shRac2 cells were co-cultured with primary mouse NK cells, and the rate of tumor cell death after co-culture was assessed using FACS, with the EL4-shβ2m co-culture group serving as the positive control. (F) Western blot was used to verify the inhibition efficiency of RAC2 in EL4 cells following treatment with EHT-1864. Additionally, the cell death rate in tumor cells was evaluated using FACS after co-culture with primary mouse NK cells. The results are representative of at least three independent experiments. Vertical bars indicate mean±SEM. Statistical significance between groups was assessed using the one-way analysis of variance with Bonferroni’s post-test, *p<0.05; **p<0.01; ***p<0.001. CFSE, Carboxyfluorescein succinimidyl ester; E:T, effector-to-target; FACS, fluorescence-activated cell sorting; h, hours; NK, natural killer; q-PCR, quantitative PCR; WT, wild type.

Techniques: Expressing, Western Blot, Knock-Out, Knockdown, Cell Culture, Co-Culture Assay, Positive Control, Inhibition, Fluorescence, FACS, Real-time Polymerase Chain Reaction

Figure 3 NK cells mediate the growth inhibition of RAC2-deficient tumors. (A–B) C57BL/6 (A) mice and BALB/c-nude (B) mice were injected subcutaneously with EL4 and EL4-sgRac2 cells, n=5 per group, and tumor growth of the mice was monitored every other day. (C) EL4, EL4-sgRac2 cells were subcutaneously inoculated on C57BL/6 mice with or without anti-NK1.1 mAb treatment (n=5 per group), and tumor growth of the mice was monitored every other day. Tumor growth curves were analyzed by two-way analysis of variance with Bonferroni’s post-test, ns, not significant; *p<0.05; **p<0.01; ***p<0.001. i.p., intraperitoneal injection; mAb, monoclonal antibody; ko, knockout; NK, natural killer; PBS, phosphate-buffered saline; wt, wild type.

Journal: Journal for immunotherapy of cancer

Article Title: RAC2 inhibition enhances tumor sensitivity to NK cell-mediated cytotoxicity.

doi: 10.1136/jitc-2024-010931

Figure Lengend Snippet: Figure 3 NK cells mediate the growth inhibition of RAC2-deficient tumors. (A–B) C57BL/6 (A) mice and BALB/c-nude (B) mice were injected subcutaneously with EL4 and EL4-sgRac2 cells, n=5 per group, and tumor growth of the mice was monitored every other day. (C) EL4, EL4-sgRac2 cells were subcutaneously inoculated on C57BL/6 mice with or without anti-NK1.1 mAb treatment (n=5 per group), and tumor growth of the mice was monitored every other day. Tumor growth curves were analyzed by two-way analysis of variance with Bonferroni’s post-test, ns, not significant; *p<0.05; **p<0.01; ***p<0.001. i.p., intraperitoneal injection; mAb, monoclonal antibody; ko, knockout; NK, natural killer; PBS, phosphate-buffered saline; wt, wild type.

Techniques: Inhibition, Injection, Knock-Out, Saline

Figure 4 RAC2 knockout in human colon cancer cells enhanced the efficacy of adoptive NK therapy. (A–C) Western blot was used to verify the RAC2 knockout efficiency. While the rate of tumor cell death after co-culture with NK-92MI cells was determined by FACS in SW620 (A), HCT116 (B) and SW480 cells (C). (D) A schematic illustration depicting the in vivo xenograft mouse model of human HCT116 colon cancer cells used for the NK cell therapy with NK-92MI cells infusion. (E) HCT116- sgScr and sgRAC2 cells were s.c. inoculated into NOD/SCID mouse (n=12). When the tumor volume reached 100 mm3, six mice from each group received an adoptive transfer of NK-92MI cells or PBS via the tail vein. Tumor growth of the mice was monitored every other day. (F) Tumors were isolated, and tumor-infiltrating NK-92MI (human-CD45+ CD56+) cells were analyzed by flow cytometry (n=3). (G) Cell death within the tumor tissues from RAC2-WT/KO tumor-bearing mice was analyzed using the TUNEL assay following treatment with NK-92MI cells (n=3). Scale bars, 50 µm. The results are representative of at least three independent experiments. Vertical bars indicate mean±SEM. Tumor growth curves were analyzed by two-way analysis of variance with Bonferroni’s post-test. Statistical significance between groups was assessed using the one-way analysis of variance with Bonferroni’s post-test, or two-tailed unpaired t-test, ns, not significant; *p<0.05; **p<0.01; ***p<0.001. CFSE, carboxyfluorescein succinimidyl ester; DAPI, 4′,6-diamidino-2-phenylindole; FACS, fluorescence-activated cell sorting; i.v., intravenous; NK, natural killer; PBS, phosphate-buffered saline; s.c., subcutaneous; TUNEL, terminal deoxynucleotidyl transferase dUTP nick end labeling.

Journal: Journal for immunotherapy of cancer

Article Title: RAC2 inhibition enhances tumor sensitivity to NK cell-mediated cytotoxicity.

doi: 10.1136/jitc-2024-010931

Figure Lengend Snippet: Figure 4 RAC2 knockout in human colon cancer cells enhanced the efficacy of adoptive NK therapy. (A–C) Western blot was used to verify the RAC2 knockout efficiency. While the rate of tumor cell death after co-culture with NK-92MI cells was determined by FACS in SW620 (A), HCT116 (B) and SW480 cells (C). (D) A schematic illustration depicting the in vivo xenograft mouse model of human HCT116 colon cancer cells used for the NK cell therapy with NK-92MI cells infusion. (E) HCT116- sgScr and sgRAC2 cells were s.c. inoculated into NOD/SCID mouse (n=12). When the tumor volume reached 100 mm3, six mice from each group received an adoptive transfer of NK-92MI cells or PBS via the tail vein. Tumor growth of the mice was monitored every other day. (F) Tumors were isolated, and tumor-infiltrating NK-92MI (human-CD45+ CD56+) cells were analyzed by flow cytometry (n=3). (G) Cell death within the tumor tissues from RAC2-WT/KO tumor-bearing mice was analyzed using the TUNEL assay following treatment with NK-92MI cells (n=3). Scale bars, 50 µm. The results are representative of at least three independent experiments. Vertical bars indicate mean±SEM. Tumor growth curves were analyzed by two-way analysis of variance with Bonferroni’s post-test. Statistical significance between groups was assessed using the one-way analysis of variance with Bonferroni’s post-test, or two-tailed unpaired t-test, ns, not significant; *p<0.05; **p<0.01; ***p<0.001. CFSE, carboxyfluorescein succinimidyl ester; DAPI, 4′,6-diamidino-2-phenylindole; FACS, fluorescence-activated cell sorting; i.v., intravenous; NK, natural killer; PBS, phosphate-buffered saline; s.c., subcutaneous; TUNEL, terminal deoxynucleotidyl transferase dUTP nick end labeling.

Techniques: Knock-Out, Western Blot, Co-Culture Assay, In Vivo, Adoptive Transfer Assay, Isolation, Flow Cytometry, TUNEL Assay, Two Tailed Test, Fluorescence, FACS, Saline

Figure 5 RAC2 ablation increases tumor sensitivity to NK cytotoxicity depending on cell-cell contact. (A–B) EL4 and EL4- sgRac2 cells were co-cultured with primary mouse NK cells, HeLa and HeLa-sgRAC2 cells were co-cultured with NK-92MI cells, with (A) or without (B) transwell chamber method, and tumor cell death rate was determined by FACS. (C–D) Confocal microscopy was used to observe the cytoskeletal morphology and F-actin fluorescence intensity of EL4, EL4-sgRac2 and EL4-shRac2 cells (n=8) (C) and SW620-sgScr, SW620-sgRAC2-1 and SW620-sgRAC2-2 cells (n=10) (D). Scale bars, 5 µm. (E–F) Confocal microscopy was used to observe the Hela and Hela-sgRAC2 cells (spindle cells) co-cultured with NK-92MI cells (round cells), representative immunofluorescent images (E) and quantitative analysis (F) for F-actin fluorescence intensity in HeLa, HeLa-sgRAC2 cells (n=11). Scale bars, 5 µm. (G) The ratio of the F-actin fluorescence intensity at the effector–target conjugate interface to the total fluorescence intensity of the unconjugated membranes. The results are representative of at least three independent experiments. Vertical bars indicate mean±SEM. Statistical significance between groups was assessed using the two-tailed t-test, or one-way analysis of variance with Bonferroni’s post-test, ns, not significant; *p<0.05; **p<0.01; ***p<0.001. DAPI, 4′,6-diamidino-2-phenylindole; FACS, fluorescence-activated cell sorting; MFI, mean fluorescence intensity; NK, natural killer; WT, wild type.

Journal: Journal for immunotherapy of cancer

Article Title: RAC2 inhibition enhances tumor sensitivity to NK cell-mediated cytotoxicity.

doi: 10.1136/jitc-2024-010931

Figure Lengend Snippet: Figure 5 RAC2 ablation increases tumor sensitivity to NK cytotoxicity depending on cell-cell contact. (A–B) EL4 and EL4- sgRac2 cells were co-cultured with primary mouse NK cells, HeLa and HeLa-sgRAC2 cells were co-cultured with NK-92MI cells, with (A) or without (B) transwell chamber method, and tumor cell death rate was determined by FACS. (C–D) Confocal microscopy was used to observe the cytoskeletal morphology and F-actin fluorescence intensity of EL4, EL4-sgRac2 and EL4-shRac2 cells (n=8) (C) and SW620-sgScr, SW620-sgRAC2-1 and SW620-sgRAC2-2 cells (n=10) (D). Scale bars, 5 µm. (E–F) Confocal microscopy was used to observe the Hela and Hela-sgRAC2 cells (spindle cells) co-cultured with NK-92MI cells (round cells), representative immunofluorescent images (E) and quantitative analysis (F) for F-actin fluorescence intensity in HeLa, HeLa-sgRAC2 cells (n=11). Scale bars, 5 µm. (G) The ratio of the F-actin fluorescence intensity at the effector–target conjugate interface to the total fluorescence intensity of the unconjugated membranes. The results are representative of at least three independent experiments. Vertical bars indicate mean±SEM. Statistical significance between groups was assessed using the two-tailed t-test, or one-way analysis of variance with Bonferroni’s post-test, ns, not significant; *p<0.05; **p<0.01; ***p<0.001. DAPI, 4′,6-diamidino-2-phenylindole; FACS, fluorescence-activated cell sorting; MFI, mean fluorescence intensity; NK, natural killer; WT, wild type.

Techniques: Cell Culture, Confocal Microscopy, Fluorescence, Two Tailed Test, FACS

Figure 6 Aspartic acid 148 residue of RAC2 is critical for IS formation and NK killing sensitivity of tumor cells. (A) Schematic re-presentation of the Rac2 truncation and mutation construction, with the truncated or mutated sites in red. (B–D) Western blot showed the construct expression in EL4 cells, EL4-sgRac2 and EL4-sgRac2+RAC2 WT/CAAX-/D148E/D150G cells (B), and tumor cells were co-cultured with primary mouse NK cells, and the tumor cell death rate was determined by FACS (C). Confocal microscopy was used to observe the cytoskeletal morphology and F-actin fluorescence intensity in EL4, EL4- sgRac2, EL4-sgRac2+RAC2 WT and EL4-sgRac2+RAC2-D148G (n=5) (D). Scale bars, 10 µm. (E–F) Kaplan-Meier analysis of RAC2 expression in relation to clinical prognosis in patients with solid tumors, specifically COAD (E), and hematological malignancies, such as AML (F), as derived from TCGA dataset. The p value was calculated using the log-rank test. The results are representative of at least three independent experiments. Vertical bars indicate mean±SEM. Statistical significance between groups was assessed using the one-way analysis of variance with Bonferroni’s post-test, ns, not significant; *p<0.05; **p<0.01; ***p<0.001. AML, acute myeloid leukemia; COAD, colon adenocarcinoma; CFSE, carboxyfluorescein succinimidyl ester; DAPI, 4′,6-diamidino-2-phenylindole; FACS, fluorescence-activated cell sorting; IS, immunological synapse; MFI, mean fluorescence intensity; NK, natural killer; TCGA, The Cancer Genome Atlas; WT, wild type.

Journal: Journal for immunotherapy of cancer

Article Title: RAC2 inhibition enhances tumor sensitivity to NK cell-mediated cytotoxicity.

doi: 10.1136/jitc-2024-010931

Figure Lengend Snippet: Figure 6 Aspartic acid 148 residue of RAC2 is critical for IS formation and NK killing sensitivity of tumor cells. (A) Schematic re-presentation of the Rac2 truncation and mutation construction, with the truncated or mutated sites in red. (B–D) Western blot showed the construct expression in EL4 cells, EL4-sgRac2 and EL4-sgRac2+RAC2 WT/CAAX-/D148E/D150G cells (B), and tumor cells were co-cultured with primary mouse NK cells, and the tumor cell death rate was determined by FACS (C). Confocal microscopy was used to observe the cytoskeletal morphology and F-actin fluorescence intensity in EL4, EL4- sgRac2, EL4-sgRac2+RAC2 WT and EL4-sgRac2+RAC2-D148G (n=5) (D). Scale bars, 10 µm. (E–F) Kaplan-Meier analysis of RAC2 expression in relation to clinical prognosis in patients with solid tumors, specifically COAD (E), and hematological malignancies, such as AML (F), as derived from TCGA dataset. The p value was calculated using the log-rank test. The results are representative of at least three independent experiments. Vertical bars indicate mean±SEM. Statistical significance between groups was assessed using the one-way analysis of variance with Bonferroni’s post-test, ns, not significant; *p<0.05; **p<0.01; ***p<0.001. AML, acute myeloid leukemia; COAD, colon adenocarcinoma; CFSE, carboxyfluorescein succinimidyl ester; DAPI, 4′,6-diamidino-2-phenylindole; FACS, fluorescence-activated cell sorting; IS, immunological synapse; MFI, mean fluorescence intensity; NK, natural killer; TCGA, The Cancer Genome Atlas; WT, wild type.

Techniques: Residue, Mutagenesis, Western Blot, Construct, Expressing, Cell Culture, Confocal Microscopy, Fluorescence, Derivative Assay, FACS

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ras related c3 botulinum toxin substrate 2 rac2 (Proteintech)

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