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fpr1 inhibitor  (MedChemExpress)


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    Structured Review

    MedChemExpress fpr1 inhibitor
    Fpr1 Inhibitor, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/fpr1 inhibitor/product/MedChemExpress
    Average 93 stars, based on 6 article reviews
    fpr1 inhibitor - by Bioz Stars, 2026-03
    93/100 stars

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    Macrophages promoted the proliferation of myxoma cells. a The number of significant ligand-receptor interactions between T cells and myxoma cells. b The number of significant ligand-receptor interactions between macrophage and myxoma cells. The direction of the arrow indicates the cell type expressing the ligand, while the direction the arrow points to represents the cell type expressing the receptor. c Barplot depicting the number of significant ligand-receptor interaction pairs (y-axis) between myxoma cells and macrophages (filled by different colors) in different pathways (x-axis). d Representative ligand-receptor pairs between myxoma cells and macrophages. The color indicates the strength of the ligand-receptor interactions, and the dot size represents the statistical significance of interactive molecular pairs. e The expression of genes is projected on the UMAP plot of macrophages. f The infographic (created with BioRender.com) summarizes predicted cell-cell interaction circuits in myxoma. g Incucyte proliferation assay of the co-culture system between myxoma cells and macrophages. h Immunofluorescence images show the proliferation of myxoma cells at different time points in the single culture and co-culture system. i Comparison of the number of myxoma cells in proliferative state at different time points in single culture and co-culture systems. j The secretion levels of some factors in a single culture and co-culture system are based on Elisa. The error bar indicates the standard error of the mean. k Comparison of myxoma cell proliferation status in the co-culture system after the addition of different inhibitors. <t>HCH6-1,</t> <t>FPR1</t> antagonist. Crenolanib, PDGFR inhibitor. *P < 0.05; **P < 0.01; ***P < 0.001
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    Macrophages promoted the proliferation of myxoma cells. a The number of significant ligand-receptor interactions between T cells and myxoma cells. b The number of significant ligand-receptor interactions between macrophage and myxoma cells. The direction of the arrow indicates the cell type expressing the ligand, while the direction the arrow points to represents the cell type expressing the receptor. c Barplot depicting the number of significant ligand-receptor interaction pairs (y-axis) between myxoma cells and macrophages (filled by different colors) in different pathways (x-axis). d Representative ligand-receptor pairs between myxoma cells and macrophages. The color indicates the strength of the ligand-receptor interactions, and the dot size represents the statistical significance of interactive molecular pairs. e The expression of genes is projected on the UMAP plot of macrophages. f The infographic (created with BioRender.com) summarizes predicted cell-cell interaction circuits in myxoma. g Incucyte proliferation assay of the co-culture system between myxoma cells and macrophages. h Immunofluorescence images show the proliferation of myxoma cells at different time points in the single culture and co-culture system. i Comparison of the number of myxoma cells in proliferative state at different time points in single culture and co-culture systems. j The secretion levels of some factors in a single culture and co-culture system are based on Elisa. The error bar indicates the standard error of the mean. k Comparison of myxoma cell proliferation status in the co-culture system after the addition of different inhibitors. <t>HCH6-1,</t> <t>FPR1</t> antagonist. Crenolanib, PDGFR inhibitor. *P < 0.05; **P < 0.01; ***P < 0.001
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    Macrophages promoted the proliferation of myxoma cells. a The number of significant ligand-receptor interactions between T cells and myxoma cells. b The number of significant ligand-receptor interactions between macrophage and myxoma cells. The direction of the arrow indicates the cell type expressing the ligand, while the direction the arrow points to represents the cell type expressing the receptor. c Barplot depicting the number of significant ligand-receptor interaction pairs (y-axis) between myxoma cells and macrophages (filled by different colors) in different pathways (x-axis). d Representative ligand-receptor pairs between myxoma cells and macrophages. The color indicates the strength of the ligand-receptor interactions, and the dot size represents the statistical significance of interactive molecular pairs. e The expression of genes is projected on the UMAP plot of macrophages. f The infographic (created with BioRender.com) summarizes predicted cell-cell interaction circuits in myxoma. g Incucyte proliferation assay of the co-culture system between myxoma cells and macrophages. h Immunofluorescence images show the proliferation of myxoma cells at different time points in the single culture and co-culture system. i Comparison of the number of myxoma cells in proliferative state at different time points in single culture and co-culture systems. j The secretion levels of some factors in a single culture and co-culture system are based on Elisa. The error bar indicates the standard error of the mean. k Comparison of myxoma cell proliferation status in the co-culture system after the addition of different inhibitors. HCH6-1, FPR1 antagonist. Crenolanib, PDGFR inhibitor. *P < 0.05; **P < 0.01; ***P < 0.001

    Journal: Signal Transduction and Targeted Therapy

    Article Title: Revealing the crucial roles of suppressive immune microenvironment in cardiac myxoma progression

    doi: 10.1038/s41392-024-01912-2

    Figure Lengend Snippet: Macrophages promoted the proliferation of myxoma cells. a The number of significant ligand-receptor interactions between T cells and myxoma cells. b The number of significant ligand-receptor interactions between macrophage and myxoma cells. The direction of the arrow indicates the cell type expressing the ligand, while the direction the arrow points to represents the cell type expressing the receptor. c Barplot depicting the number of significant ligand-receptor interaction pairs (y-axis) between myxoma cells and macrophages (filled by different colors) in different pathways (x-axis). d Representative ligand-receptor pairs between myxoma cells and macrophages. The color indicates the strength of the ligand-receptor interactions, and the dot size represents the statistical significance of interactive molecular pairs. e The expression of genes is projected on the UMAP plot of macrophages. f The infographic (created with BioRender.com) summarizes predicted cell-cell interaction circuits in myxoma. g Incucyte proliferation assay of the co-culture system between myxoma cells and macrophages. h Immunofluorescence images show the proliferation of myxoma cells at different time points in the single culture and co-culture system. i Comparison of the number of myxoma cells in proliferative state at different time points in single culture and co-culture systems. j The secretion levels of some factors in a single culture and co-culture system are based on Elisa. The error bar indicates the standard error of the mean. k Comparison of myxoma cell proliferation status in the co-culture system after the addition of different inhibitors. HCH6-1, FPR1 antagonist. Crenolanib, PDGFR inhibitor. *P < 0.05; **P < 0.01; ***P < 0.001

    Article Snippet: In the inhibitor-related experiments, we added DMSO, the FPR1 antagonist HCH6-1 (5 μM, Selleck, Cat. No. S0547), and the PDGFR inhibitor Crenolanib (50 nM, Selleck, Cat. No. S2730) to the co-culture system.

    Techniques: Expressing, Proliferation Assay, Co-Culture Assay, Immunofluorescence, Comparison, Enzyme-linked Immunosorbent Assay

    Fig. 7 Schematic diagram of the invasion zone. Schematic diagram showing the local ecosystem where tumor cells with high invasiveness (CXCL6+ tumor cells), damaged hepatocytes (SAAs+ hepatocytes) and recruited FPR1+ macrophages polarizing into the M2 phenotype interacted in the 500 µm-wide invasive zone, contributing to tumor progression.

    Journal: Cell research

    Article Title: An invasive zone in human liver cancer identified by Stereo-seq promotes hepatocyte-tumor cell crosstalk, local immunosuppression and tumor progression.

    doi: 10.1038/s41422-023-00831-1

    Figure Lengend Snippet: Fig. 7 Schematic diagram of the invasion zone. Schematic diagram showing the local ecosystem where tumor cells with high invasiveness (CXCL6+ tumor cells), damaged hepatocytes (SAAs+ hepatocytes) and recruited FPR1+ macrophages polarizing into the M2 phenotype interacted in the 500 µm-wide invasive zone, contributing to tumor progression.

    Article Snippet: FPR1 inhibitor HCH6-1 (#HY-101283, MedChemExpress, Shanghai, China) was added in the medium with a concentration of 3 μM in the lower compartments of transwell chambers.

    Techniques: