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ccl2 synthesis inhibitor bindarit  (MedChemExpress)


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    Structured Review

    MedChemExpress ccl2 synthesis inhibitor bindarit
    A) Volcano plot of Nomic Bio Core Immune panel (268 cytokines) in DMSO and BrdU CM from astrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). B) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from endothelial cells showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). C) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from microglia showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). D) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from oligodendrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). E) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from neurons showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). F) Venn diagram showing the number of upregulated factors specifically in astrocyte BrdU CM and microglia BrdU CM (69) as well as the commonly upregulated factors . G) Z-score heatmap showing selected Core Immune panel (Nomic Bio) cytokine expression in all cell types (endothelial cells (pink), microglia (yellow), oligodendrocytes (green), astrocytes (purple), and neurons (blue)) based on nELISA analysis of CM from DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). H) Normalized expression of <t>CCL2</t> based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). Normalized expression of MIF based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). I) Normalized nELISA signal of CCL2 in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Normalized nELISA signal of MIF in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (H) and two-way ANOVA with Šídák’s multiple comparisons test (I). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, *** p<0.001).
    Ccl2 Synthesis Inhibitor Bindarit, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 29 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ccl2+synthesis+inhibitor+bindarit/bio_rxiv__64898__2026__02__10__705129-246-3-7?v=MedChemExpress
    Average 95 stars, based on 29 article reviews
    ccl2 synthesis inhibitor bindarit - by Bioz Stars, 2026-08
    95/100 stars

    Images

    1) Product Images from "Characterizing the SASP-Dependent Paracrine Spreading of Senescence Between Human Brain Cell Types"

    Article Title: Characterizing the SASP-Dependent Paracrine Spreading of Senescence Between Human Brain Cell Types

    Journal: bioRxiv

    doi: 10.64898/2026.02.10.705129

    A) Volcano plot of Nomic Bio Core Immune panel (268 cytokines) in DMSO and BrdU CM from astrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). B) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from endothelial cells showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). C) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from microglia showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). D) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from oligodendrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). E) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from neurons showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). F) Venn diagram showing the number of upregulated factors specifically in astrocyte BrdU CM and microglia BrdU CM (69) as well as the commonly upregulated factors . G) Z-score heatmap showing selected Core Immune panel (Nomic Bio) cytokine expression in all cell types (endothelial cells (pink), microglia (yellow), oligodendrocytes (green), astrocytes (purple), and neurons (blue)) based on nELISA analysis of CM from DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). H) Normalized expression of CCL2 based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). Normalized expression of MIF based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). I) Normalized nELISA signal of CCL2 in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Normalized nELISA signal of MIF in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (H) and two-way ANOVA with Šídák’s multiple comparisons test (I). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, *** p<0.001).
    Figure Legend Snippet: A) Volcano plot of Nomic Bio Core Immune panel (268 cytokines) in DMSO and BrdU CM from astrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). B) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from endothelial cells showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). C) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from microglia showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). D) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from oligodendrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). E) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from neurons showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). F) Venn diagram showing the number of upregulated factors specifically in astrocyte BrdU CM and microglia BrdU CM (69) as well as the commonly upregulated factors . G) Z-score heatmap showing selected Core Immune panel (Nomic Bio) cytokine expression in all cell types (endothelial cells (pink), microglia (yellow), oligodendrocytes (green), astrocytes (purple), and neurons (blue)) based on nELISA analysis of CM from DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). H) Normalized expression of CCL2 based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). Normalized expression of MIF based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). I) Normalized nELISA signal of CCL2 in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Normalized nELISA signal of MIF in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (H) and two-way ANOVA with Šídák’s multiple comparisons test (I). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, *** p<0.001).

    Techniques Used: Expressing, Standard Deviation

    A) Schematic depicting BulkSignalR pipeline which uses known ligand-receptor interactions and affected downstream pathways to analyze their activation based on our bulk RNAseq data from DMSO and BrdU treated human cell lines (created with BioRender). B) Venn diagram showing the number of receptors inferred from BulkSignalR to be activated across each of the five human cell types. Three receptors were identified in common between astrocytes (purple), endothelial cells (pink), and microglia (yellow) which were the cell types shown to be capable of receiving senescence signals and becoming SA β-gal positive: CXCR7, KREMEN2, and GIPR. Only CXCR7 was expressed in the cell types capable of entering secondary senescence (astrocytes, endothelial cells, microglia) ( , S3B). C) TPM expression values of CXCR7 , its ligand CXCL12 , and DPP4 which cleaves and inactivates CXCL12 in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). D) Schematic of the four selected SASP inhibitors mechanisms of action: Bindarit is a CCL2 synthesis inhibitor which prevents p65 activation of the CCL2 gene at the promoter region, ISO-1 is a MIF antagonist, ACT-1004-1239 is a CXCR7 antagonist, and Sitagliptin inhibits DPP4 preventing its action of cleaving and inactivating CXCL12 (created with BioRender). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (C). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, ** p<0.01, *** p<0.001).
    Figure Legend Snippet: A) Schematic depicting BulkSignalR pipeline which uses known ligand-receptor interactions and affected downstream pathways to analyze their activation based on our bulk RNAseq data from DMSO and BrdU treated human cell lines (created with BioRender). B) Venn diagram showing the number of receptors inferred from BulkSignalR to be activated across each of the five human cell types. Three receptors were identified in common between astrocytes (purple), endothelial cells (pink), and microglia (yellow) which were the cell types shown to be capable of receiving senescence signals and becoming SA β-gal positive: CXCR7, KREMEN2, and GIPR. Only CXCR7 was expressed in the cell types capable of entering secondary senescence (astrocytes, endothelial cells, microglia) ( , S3B). C) TPM expression values of CXCR7 , its ligand CXCL12 , and DPP4 which cleaves and inactivates CXCL12 in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). D) Schematic of the four selected SASP inhibitors mechanisms of action: Bindarit is a CCL2 synthesis inhibitor which prevents p65 activation of the CCL2 gene at the promoter region, ISO-1 is a MIF antagonist, ACT-1004-1239 is a CXCR7 antagonist, and Sitagliptin inhibits DPP4 preventing its action of cleaving and inactivating CXCL12 (created with BioRender). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (C). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, ** p<0.01, *** p<0.001).

    Techniques Used: Activation Assay, RNA sequencing, Expressing, Standard Deviation

    A) TPM expression values of CCL2 receptors CCR1, CCR4, CCRL2, and ACKR1 in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). B) TPM expression values of receptors KREMEN2 and GIPR in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (A-B). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, * p<0.05, ** p<0.01, *** p<0.001).
    Figure Legend Snippet: A) TPM expression values of CCL2 receptors CCR1, CCR4, CCRL2, and ACKR1 in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). B) TPM expression values of receptors KREMEN2 and GIPR in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (A-B). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, * p<0.05, ** p<0.01, *** p<0.001).

    Techniques Used: Expressing, Standard Deviation



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    95
    MedChemExpress ccl2 synthesis inhibitor bindarit
    A) Volcano plot of Nomic Bio Core Immune panel (268 cytokines) in DMSO and BrdU CM from astrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). B) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from endothelial cells showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). C) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from microglia showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). D) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from oligodendrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). E) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from neurons showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). F) Venn diagram showing the number of upregulated factors specifically in astrocyte BrdU CM and microglia BrdU CM (69) as well as the commonly upregulated factors . G) Z-score heatmap showing selected Core Immune panel (Nomic Bio) cytokine expression in all cell types (endothelial cells (pink), microglia (yellow), oligodendrocytes (green), astrocytes (purple), and neurons (blue)) based on nELISA analysis of CM from DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). H) Normalized expression of <t>CCL2</t> based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). Normalized expression of MIF based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). I) Normalized nELISA signal of CCL2 in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Normalized nELISA signal of MIF in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (H) and two-way ANOVA with Šídák’s multiple comparisons test (I). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, *** p<0.001).
    Ccl2 Synthesis Inhibitor Bindarit, 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
    https://www.bioz.com/product/ccl2+synthesis+inhibitor+bindarit/bio_rxiv__64898__2026__02__10__705129-246-3-7?v=MedChemExpress
    Average 95 stars, based on 1 article reviews
    ccl2 synthesis inhibitor bindarit - by Bioz Stars, 2026-08
    95/100 stars
      Buy from Supplier

    90
    Cayman Chemical ccl2 synthesis inhibitor, bindarit
    ( A ) Illustration <t>of</t> <t>Transwell</t> migration assessment of BM cells in the presence of CCL2 inhibitor <t>bindarit</t> (shown as the green bars). CCL2 inhibition with 50 μM (0.1% DMSO), 100 μM (0.2% DMSO), and 300 μM (0.6% DMSO) of bindarit was performed for 4 h before migration. As control 0.6% DMSO was used. ( B ) Representative images of Transwell migration of BM cells in the presence of bindarit. ( C ) The number of migrating BM cells among the different tumor/stroma cocultures in the presence of bindarit (300 μM). ( D – F ) The comparison of BM cell migration in different concentrations of bindarit in +HDF, +PDS1, and +PDS2. ( G ) Illustration of Transwell migration assessment of BM cells pretreated with CCR2 antagonist RS 102895 (20 μM) for 1 h. ( H ) Representative images of Transwell migration of BM cells pretreated with RS 102895. ( I ) The number of BM cells migrating after the treatment with RS 102895 (20 μM) in the different tumor/stroma cocultures. +HDF, HSC-2 + HDF coculture; +PDS1, HSC-2 + PDS1 coculture; +PDS2, HSC-2 + PDS2 coculture (5 fields per group, n = 3). All data are shown as mean ± SD. Statistical analyses were performed using Student’s t test for comparison of 2 groups and 1-way ANOVA followed by Tukey’s multiple-comparison post hoc test for comparison of more than 2 groups; * P < 0.05 ** P < 0.01, *** P < 0.001.
    Ccl2 Synthesis Inhibitor, Bindarit, supplied by Cayman Chemical, 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/product/ccl2+synthesis+inhibitor+bindarit/pmc08765046-212-8-9?v=Cayman+Chemical
    Average 90 stars, based on 1 article reviews
    ccl2 synthesis inhibitor, bindarit - by Bioz Stars, 2026-08
    90/100 stars
      Buy from Supplier

    Image Search Results


    A) Volcano plot of Nomic Bio Core Immune panel (268 cytokines) in DMSO and BrdU CM from astrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). B) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from endothelial cells showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). C) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from microglia showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). D) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from oligodendrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). E) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from neurons showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). F) Venn diagram showing the number of upregulated factors specifically in astrocyte BrdU CM and microglia BrdU CM (69) as well as the commonly upregulated factors . G) Z-score heatmap showing selected Core Immune panel (Nomic Bio) cytokine expression in all cell types (endothelial cells (pink), microglia (yellow), oligodendrocytes (green), astrocytes (purple), and neurons (blue)) based on nELISA analysis of CM from DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). H) Normalized expression of CCL2 based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). Normalized expression of MIF based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). I) Normalized nELISA signal of CCL2 in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Normalized nELISA signal of MIF in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (H) and two-way ANOVA with Šídák’s multiple comparisons test (I). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, *** p<0.001).

    Journal: bioRxiv

    Article Title: Characterizing the SASP-Dependent Paracrine Spreading of Senescence Between Human Brain Cell Types

    doi: 10.64898/2026.02.10.705129

    Figure Lengend Snippet: A) Volcano plot of Nomic Bio Core Immune panel (268 cytokines) in DMSO and BrdU CM from astrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). B) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from endothelial cells showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). C) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from microglia showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). D) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from oligodendrocytes showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). E) Volcano plot of Nomic Bio Core Immune panel cytokines in DMSO and BrdU CM from neurons showing factors that are upregulated in BrdU CM treated (red) (log2fc > 1, p-value < 0.05) and downregulated in BrdU CM treated (blue) (log2fc < -1, p-value < 0.05). Black data points indicate factors that do not reach the threshold (−1 < log2fc < 1 | p-value > 0.05). F) Venn diagram showing the number of upregulated factors specifically in astrocyte BrdU CM and microglia BrdU CM (69) as well as the commonly upregulated factors . G) Z-score heatmap showing selected Core Immune panel (Nomic Bio) cytokine expression in all cell types (endothelial cells (pink), microglia (yellow), oligodendrocytes (green), astrocytes (purple), and neurons (blue)) based on nELISA analysis of CM from DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). H) Normalized expression of CCL2 based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). Normalized expression of MIF based on human cytokine array in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, and microglia (n=4 replicates). I) Normalized nELISA signal of CCL2 in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Normalized nELISA signal of MIF in DMSO CM (grey) and BrdU CM (red) from astrocytes, endothelial cells, microglia, oligodendrocytes, and neurons (n=3 replicates). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (H) and two-way ANOVA with Šídák’s multiple comparisons test (I). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, *** p<0.001).

    Article Snippet: Treatment with the CCL2 synthesis inhibitor Bindarit (MedChemExpress, Catalog No. HY-B0498) ( ) was used to specifically target CCL2 production in senescent cells.

    Techniques: Expressing, Standard Deviation

    A) Schematic depicting BulkSignalR pipeline which uses known ligand-receptor interactions and affected downstream pathways to analyze their activation based on our bulk RNAseq data from DMSO and BrdU treated human cell lines (created with BioRender). B) Venn diagram showing the number of receptors inferred from BulkSignalR to be activated across each of the five human cell types. Three receptors were identified in common between astrocytes (purple), endothelial cells (pink), and microglia (yellow) which were the cell types shown to be capable of receiving senescence signals and becoming SA β-gal positive: CXCR7, KREMEN2, and GIPR. Only CXCR7 was expressed in the cell types capable of entering secondary senescence (astrocytes, endothelial cells, microglia) ( , S3B). C) TPM expression values of CXCR7 , its ligand CXCL12 , and DPP4 which cleaves and inactivates CXCL12 in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). D) Schematic of the four selected SASP inhibitors mechanisms of action: Bindarit is a CCL2 synthesis inhibitor which prevents p65 activation of the CCL2 gene at the promoter region, ISO-1 is a MIF antagonist, ACT-1004-1239 is a CXCR7 antagonist, and Sitagliptin inhibits DPP4 preventing its action of cleaving and inactivating CXCL12 (created with BioRender). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (C). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, ** p<0.01, *** p<0.001).

    Journal: bioRxiv

    Article Title: Characterizing the SASP-Dependent Paracrine Spreading of Senescence Between Human Brain Cell Types

    doi: 10.64898/2026.02.10.705129

    Figure Lengend Snippet: A) Schematic depicting BulkSignalR pipeline which uses known ligand-receptor interactions and affected downstream pathways to analyze their activation based on our bulk RNAseq data from DMSO and BrdU treated human cell lines (created with BioRender). B) Venn diagram showing the number of receptors inferred from BulkSignalR to be activated across each of the five human cell types. Three receptors were identified in common between astrocytes (purple), endothelial cells (pink), and microglia (yellow) which were the cell types shown to be capable of receiving senescence signals and becoming SA β-gal positive: CXCR7, KREMEN2, and GIPR. Only CXCR7 was expressed in the cell types capable of entering secondary senescence (astrocytes, endothelial cells, microglia) ( , S3B). C) TPM expression values of CXCR7 , its ligand CXCL12 , and DPP4 which cleaves and inactivates CXCL12 in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). D) Schematic of the four selected SASP inhibitors mechanisms of action: Bindarit is a CCL2 synthesis inhibitor which prevents p65 activation of the CCL2 gene at the promoter region, ISO-1 is a MIF antagonist, ACT-1004-1239 is a CXCR7 antagonist, and Sitagliptin inhibits DPP4 preventing its action of cleaving and inactivating CXCL12 (created with BioRender). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (C). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, ** p<0.01, *** p<0.001).

    Article Snippet: Treatment with the CCL2 synthesis inhibitor Bindarit (MedChemExpress, Catalog No. HY-B0498) ( ) was used to specifically target CCL2 production in senescent cells.

    Techniques: Activation Assay, RNA sequencing, Expressing, Standard Deviation

    A) TPM expression values of CCL2 receptors CCR1, CCR4, CCRL2, and ACKR1 in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). B) TPM expression values of receptors KREMEN2 and GIPR in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (A-B). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, * p<0.05, ** p<0.01, *** p<0.001).

    Journal: bioRxiv

    Article Title: Characterizing the SASP-Dependent Paracrine Spreading of Senescence Between Human Brain Cell Types

    doi: 10.64898/2026.02.10.705129

    Figure Lengend Snippet: A) TPM expression values of CCL2 receptors CCR1, CCR4, CCRL2, and ACKR1 in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). B) TPM expression values of receptors KREMEN2 and GIPR in DMSO (grey) and BrdU (red) treated cell lines (n=3 replicates). Data was analyzed by two-way ANOVA with Tukey’s multiple comparisons test (A-B). All graphs show mean with error bars depicting standard deviation (ns, p>0.05, * p<0.05, ** p<0.01, *** p<0.001).

    Article Snippet: Treatment with the CCL2 synthesis inhibitor Bindarit (MedChemExpress, Catalog No. HY-B0498) ( ) was used to specifically target CCL2 production in senescent cells.

    Techniques: Expressing, Standard Deviation

    ( A ) Illustration of Transwell migration assessment of BM cells in the presence of CCL2 inhibitor bindarit (shown as the green bars). CCL2 inhibition with 50 μM (0.1% DMSO), 100 μM (0.2% DMSO), and 300 μM (0.6% DMSO) of bindarit was performed for 4 h before migration. As control 0.6% DMSO was used. ( B ) Representative images of Transwell migration of BM cells in the presence of bindarit. ( C ) The number of migrating BM cells among the different tumor/stroma cocultures in the presence of bindarit (300 μM). ( D – F ) The comparison of BM cell migration in different concentrations of bindarit in +HDF, +PDS1, and +PDS2. ( G ) Illustration of Transwell migration assessment of BM cells pretreated with CCR2 antagonist RS 102895 (20 μM) for 1 h. ( H ) Representative images of Transwell migration of BM cells pretreated with RS 102895. ( I ) The number of BM cells migrating after the treatment with RS 102895 (20 μM) in the different tumor/stroma cocultures. +HDF, HSC-2 + HDF coculture; +PDS1, HSC-2 + PDS1 coculture; +PDS2, HSC-2 + PDS2 coculture (5 fields per group, n = 3). All data are shown as mean ± SD. Statistical analyses were performed using Student’s t test for comparison of 2 groups and 1-way ANOVA followed by Tukey’s multiple-comparison post hoc test for comparison of more than 2 groups; * P < 0.05 ** P < 0.01, *** P < 0.001.

    Journal: JCI Insight

    Article Title: Resident stroma-secreted chemokine CCL2 governs myeloid-derived suppressor cells in the tumor microenvironment

    doi: 10.1172/jci.insight.148960

    Figure Lengend Snippet: ( A ) Illustration of Transwell migration assessment of BM cells in the presence of CCL2 inhibitor bindarit (shown as the green bars). CCL2 inhibition with 50 μM (0.1% DMSO), 100 μM (0.2% DMSO), and 300 μM (0.6% DMSO) of bindarit was performed for 4 h before migration. As control 0.6% DMSO was used. ( B ) Representative images of Transwell migration of BM cells in the presence of bindarit. ( C ) The number of migrating BM cells among the different tumor/stroma cocultures in the presence of bindarit (300 μM). ( D – F ) The comparison of BM cell migration in different concentrations of bindarit in +HDF, +PDS1, and +PDS2. ( G ) Illustration of Transwell migration assessment of BM cells pretreated with CCR2 antagonist RS 102895 (20 μM) for 1 h. ( H ) Representative images of Transwell migration of BM cells pretreated with RS 102895. ( I ) The number of BM cells migrating after the treatment with RS 102895 (20 μM) in the different tumor/stroma cocultures. +HDF, HSC-2 + HDF coculture; +PDS1, HSC-2 + PDS1 coculture; +PDS2, HSC-2 + PDS2 coculture (5 fields per group, n = 3). All data are shown as mean ± SD. Statistical analyses were performed using Student’s t test for comparison of 2 groups and 1-way ANOVA followed by Tukey’s multiple-comparison post hoc test for comparison of more than 2 groups; * P < 0.05 ** P < 0.01, *** P < 0.001.

    Article Snippet: Transwell migration was analyzed using CCL2 synthesis inhibitor, bindarit (Cayman Chemical Company), or CCR2 antagonist RS 102895 hydrochloride (Cayman Chemical Company).

    Techniques: Migration, Inhibition, Control, Comparison