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il 6 detection kit  (Boster Bio)


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    Structured Review

    Boster Bio il 6 detection kit
    In vivo study in anti-tumor immune response by analysizing the maturation, activation and infiltration of immune-related cells, as well as the level of immune-related cytokines. (A) The maturation of DCs in lymph nodes of mice; (B) The activation of CD4 + /CD8 + T cells in spleens in of mice; (C) The activation of NK cells from spleens of mice. (D–G) The quantitative analysis of flow cytometry, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001. (H) Immunofluorescence photos of CD4 + and CD8 + T cell infiltrating tumor tissues of mice, bar: 100 μm. (I–K) The quantitative analysis of immune-related cytokines: <t>IL-6,</t> TNF-α and IFN-γ, ∗ p < 0.5, ∗∗ p < 0.01, ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001.
    Il 6 Detection Kit, supplied by Boster Bio, used in various techniques. Bioz Stars score: 96/100, based on 1373 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/il+6+detection+kit/Mouse+IL-6%2FInterleukin-6+PicoKine+Quick+ELISA+Kit/pmc12874101-54-13-19
    Average 96 stars, based on 1373 article reviews
    il 6 detection kit - by Bioz Stars, 2026-09
    96/100 stars

    Images

    1) Product Images from "Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy"

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy

    Journal: Materials Today Bio

    doi: 10.1016/j.mtbio.2026.102824

    In vivo study in anti-tumor immune response by analysizing the maturation, activation and infiltration of immune-related cells, as well as the level of immune-related cytokines. (A) The maturation of DCs in lymph nodes of mice; (B) The activation of CD4 + /CD8 + T cells in spleens in of mice; (C) The activation of NK cells from spleens of mice. (D–G) The quantitative analysis of flow cytometry, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001. (H) Immunofluorescence photos of CD4 + and CD8 + T cell infiltrating tumor tissues of mice, bar: 100 μm. (I–K) The quantitative analysis of immune-related cytokines: IL-6, TNF-α and IFN-γ, ∗ p < 0.5, ∗∗ p < 0.01, ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001.
    Figure Legend Snippet: In vivo study in anti-tumor immune response by analysizing the maturation, activation and infiltration of immune-related cells, as well as the level of immune-related cytokines. (A) The maturation of DCs in lymph nodes of mice; (B) The activation of CD4 + /CD8 + T cells in spleens in of mice; (C) The activation of NK cells from spleens of mice. (D–G) The quantitative analysis of flow cytometry, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001. (H) Immunofluorescence photos of CD4 + and CD8 + T cell infiltrating tumor tissues of mice, bar: 100 μm. (I–K) The quantitative analysis of immune-related cytokines: IL-6, TNF-α and IFN-γ, ∗ p < 0.5, ∗∗ p < 0.01, ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001.

    Techniques Used: In Vivo, Activation Assay, Flow Cytometry, Immunofluorescence

    In vivo anti-tumor immune mechanisim analysis of BU-CDs CA-HA -loaded Janus membrane under NIR: (A–I) Flow cytometry and quantitative analysis of DCs, CD4 + /CD8 + T cells, NK cells and MDSCs, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001; (J) Immunofluorescent staining of CD4 + /CD8 + T cells in tumor tissues to illustrate the enhanced tumor-specific identification and infiltration of T cells, bar: 50 μm; (K–L) Elisa test of proinflammatory cytokin (IL-6, TNF-α and IFN-γ) to assess the inflammatory activity, ∗ p < 0.05, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
    Figure Legend Snippet: In vivo anti-tumor immune mechanisim analysis of BU-CDs CA-HA -loaded Janus membrane under NIR: (A–I) Flow cytometry and quantitative analysis of DCs, CD4 + /CD8 + T cells, NK cells and MDSCs, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001; (J) Immunofluorescent staining of CD4 + /CD8 + T cells in tumor tissues to illustrate the enhanced tumor-specific identification and infiltration of T cells, bar: 50 μm; (K–L) Elisa test of proinflammatory cytokin (IL-6, TNF-α and IFN-γ) to assess the inflammatory activity, ∗ p < 0.05, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

    Techniques Used: In Vivo, Membrane, Flow Cytometry, Staining, Enzyme-linked Immunosorbent Assay, Activity Assay

    Related Articles

    In Vivo:

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Activation Assay:

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Flow Cytometry:

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Immunofluorescence:

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Membrane:

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Staining:

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Enzyme-linked Immunosorbent Assay:

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Activity Assay:

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy
    Article Snippet: The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).The terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay kit was purchased from Roche (Switzerland).. The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).



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    Image Search Results


    In vivo study in anti-tumor immune response by analysizing the maturation, activation and infiltration of immune-related cells, as well as the level of immune-related cytokines. (A) The maturation of DCs in lymph nodes of mice; (B) The activation of CD4 + /CD8 + T cells in spleens in of mice; (C) The activation of NK cells from spleens of mice. (D–G) The quantitative analysis of flow cytometry, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001. (H) Immunofluorescence photos of CD4 + and CD8 + T cell infiltrating tumor tissues of mice, bar: 100 μm. (I–K) The quantitative analysis of immune-related cytokines: IL-6, TNF-α and IFN-γ, ∗ p < 0.5, ∗∗ p < 0.01, ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy

    doi: 10.1016/j.mtbio.2026.102824

    Figure Lengend Snippet: In vivo study in anti-tumor immune response by analysizing the maturation, activation and infiltration of immune-related cells, as well as the level of immune-related cytokines. (A) The maturation of DCs in lymph nodes of mice; (B) The activation of CD4 + /CD8 + T cells in spleens in of mice; (C) The activation of NK cells from spleens of mice. (D–G) The quantitative analysis of flow cytometry, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001. (H) Immunofluorescence photos of CD4 + and CD8 + T cell infiltrating tumor tissues of mice, bar: 100 μm. (I–K) The quantitative analysis of immune-related cytokines: IL-6, TNF-α and IFN-γ, ∗ p < 0.5, ∗∗ p < 0.01, ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001.

    Article Snippet: The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Techniques: In Vivo, Activation Assay, Flow Cytometry, Immunofluorescence

    In vivo anti-tumor immune mechanisim analysis of BU-CDs CA-HA -loaded Janus membrane under NIR: (A–I) Flow cytometry and quantitative analysis of DCs, CD4 + /CD8 + T cells, NK cells and MDSCs, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001; (J) Immunofluorescent staining of CD4 + /CD8 + T cells in tumor tissues to illustrate the enhanced tumor-specific identification and infiltration of T cells, bar: 50 μm; (K–L) Elisa test of proinflammatory cytokin (IL-6, TNF-α and IFN-γ) to assess the inflammatory activity, ∗ p < 0.05, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Immediate tumor killing and long-term anti-tumor immunoreaction induced by Bufalin-loaded phototherapeutic Janus membrane in CRC postoperative therapy

    doi: 10.1016/j.mtbio.2026.102824

    Figure Lengend Snippet: In vivo anti-tumor immune mechanisim analysis of BU-CDs CA-HA -loaded Janus membrane under NIR: (A–I) Flow cytometry and quantitative analysis of DCs, CD4 + /CD8 + T cells, NK cells and MDSCs, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001; (J) Immunofluorescent staining of CD4 + /CD8 + T cells in tumor tissues to illustrate the enhanced tumor-specific identification and infiltration of T cells, bar: 50 μm; (K–L) Elisa test of proinflammatory cytokin (IL-6, TNF-α and IFN-γ) to assess the inflammatory activity, ∗ p < 0.05, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

    Article Snippet: The IFN-γ and TNF-α detection kit was purchased from Biodragon Biotechnology (Beijing), the IL-6 detection kit was obtained from BOSTER Biotechnology (Wuhan).

    Techniques: In Vivo, Membrane, Flow Cytometry, Staining, Enzyme-linked Immunosorbent Assay, Activity Assay

    HCP alleviates oxidative stress and systemic inflammatory response in HIRI. ( A ) Malondialdehyde (MDA) content in liver tissues at 24 h reperfusion ( n = 8). ( B ) Superoxide dismutase (SOD) activity in liver tissues at 24 h reperfusion ( n = 8). ( C , D ) Serum levels of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) at 24 h reperfusion ( n = 8). ( E ) Western blot analysis of inflammatory cytokine protein expression (IL-6, TNF-α, IL-1β) in liver tissues, with GAPDH as loading control (representative of three independent experiments). Data are mean ± SD. Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. Vehicle group.

    Journal: Biomedicines

    Article Title: Houttuynia cordata Polysaccharide Alleviates Hepatic Ischemia-Reperfusion Injury by Regulating Macrophage Polarization via Inhibiting the TLR4/NF-κB Signaling Pathway

    doi: 10.3390/biomedicines14020433

    Figure Lengend Snippet: HCP alleviates oxidative stress and systemic inflammatory response in HIRI. ( A ) Malondialdehyde (MDA) content in liver tissues at 24 h reperfusion ( n = 8). ( B ) Superoxide dismutase (SOD) activity in liver tissues at 24 h reperfusion ( n = 8). ( C , D ) Serum levels of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) at 24 h reperfusion ( n = 8). ( E ) Western blot analysis of inflammatory cytokine protein expression (IL-6, TNF-α, IL-1β) in liver tissues, with GAPDH as loading control (representative of three independent experiments). Data are mean ± SD. Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. Vehicle group.

    Article Snippet: Mouse ALT, AST, MDA, SOD, TNF-α, and IL-6 ELISA detection kits were purchased from Nanjing Jiancheng Bioengineering Institute (Nanjing, China).

    Techniques: Activity Assay, Western Blot, Expressing, Control

    HCP inhibits the TLR4/MyD88/NF-κB signaling pathway in HIRI, and its effects are reversed by TLR4 blockade. ( A ) Western blot analysis of TLR4, MyD88, total p65, and phospho-p65 (p-p65) protein expression in liver tissues at 24 h reperfusion. GAPDH served as loading control (representative blot of n = 3 independent samples/group). ( B ) Immunohistochemical staining for NF-κB p65 in liver sections (scale bar: 50 μm). Arrows indicate nuclear p65 staining. ( C – F ) Serum ALT, AST, TNF-α, and IL-6 levels at 24 h reperfusion in mice pretreated with or without the TLR4 inhibitor TAK-242 (3 mg/kg, i.p.) 1 h before ischemia ( n = 8). ( G ) Representative H&E-stained liver sections from corresponding groups (scale bar: 200 μm). ( H ) Western blot analysis of cytokine expression in liver tissues with or without TAK-242 intervention (representative of three experiments). Data are mean ± SD. Statistical analysis: one-way ANOVA with Tukey’s test. ** p < 0.01, **** p < 0.0001; ns, not significant.

    Journal: Biomedicines

    Article Title: Houttuynia cordata Polysaccharide Alleviates Hepatic Ischemia-Reperfusion Injury by Regulating Macrophage Polarization via Inhibiting the TLR4/NF-κB Signaling Pathway

    doi: 10.3390/biomedicines14020433

    Figure Lengend Snippet: HCP inhibits the TLR4/MyD88/NF-κB signaling pathway in HIRI, and its effects are reversed by TLR4 blockade. ( A ) Western blot analysis of TLR4, MyD88, total p65, and phospho-p65 (p-p65) protein expression in liver tissues at 24 h reperfusion. GAPDH served as loading control (representative blot of n = 3 independent samples/group). ( B ) Immunohistochemical staining for NF-κB p65 in liver sections (scale bar: 50 μm). Arrows indicate nuclear p65 staining. ( C – F ) Serum ALT, AST, TNF-α, and IL-6 levels at 24 h reperfusion in mice pretreated with or without the TLR4 inhibitor TAK-242 (3 mg/kg, i.p.) 1 h before ischemia ( n = 8). ( G ) Representative H&E-stained liver sections from corresponding groups (scale bar: 200 μm). ( H ) Western blot analysis of cytokine expression in liver tissues with or without TAK-242 intervention (representative of three experiments). Data are mean ± SD. Statistical analysis: one-way ANOVA with Tukey’s test. ** p < 0.01, **** p < 0.0001; ns, not significant.

    Article Snippet: Mouse ALT, AST, MDA, SOD, TNF-α, and IL-6 ELISA detection kits were purchased from Nanjing Jiancheng Bioengineering Institute (Nanjing, China).

    Techniques: Western Blot, Expressing, Control, Immunohistochemical staining, Staining

    HCP directly protects macrophages against hypoxia/reoxygenation (H/R) injury in a TLR4-dependent manner in vitro. ( A ) Cell viability of RAW264.7 macrophages assessed by CCK-8 assay after H/R (6 h hypoxia/12 h reoxygenation) with or without HCP co-treatment ( n = 6 independent wells per group). ( B , C ) ELISA measurement of TNF-α and IL-6 levels in culture supernatants after H/R ( n = 4 independent experiments). ( D ) Intracellular reactive oxygen species (ROS) levels measured by DCFH-DA fluorescence ( n = 4). ( E – G ) Corresponding TNF-α, IL-6, and ROS levels in cells pretreated with the TLR4 inhibitor TAK-242 (1 μM) 1 h prior to HCP and H/R ( n = 4). Data are mean ± SD. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. H/R (Vehicle) group; ns, not significant (one-way ANOVA with Tukey’s test).

    Journal: Biomedicines

    Article Title: Houttuynia cordata Polysaccharide Alleviates Hepatic Ischemia-Reperfusion Injury by Regulating Macrophage Polarization via Inhibiting the TLR4/NF-κB Signaling Pathway

    doi: 10.3390/biomedicines14020433

    Figure Lengend Snippet: HCP directly protects macrophages against hypoxia/reoxygenation (H/R) injury in a TLR4-dependent manner in vitro. ( A ) Cell viability of RAW264.7 macrophages assessed by CCK-8 assay after H/R (6 h hypoxia/12 h reoxygenation) with or without HCP co-treatment ( n = 6 independent wells per group). ( B , C ) ELISA measurement of TNF-α and IL-6 levels in culture supernatants after H/R ( n = 4 independent experiments). ( D ) Intracellular reactive oxygen species (ROS) levels measured by DCFH-DA fluorescence ( n = 4). ( E – G ) Corresponding TNF-α, IL-6, and ROS levels in cells pretreated with the TLR4 inhibitor TAK-242 (1 μM) 1 h prior to HCP and H/R ( n = 4). Data are mean ± SD. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. H/R (Vehicle) group; ns, not significant (one-way ANOVA with Tukey’s test).

    Article Snippet: Mouse ALT, AST, MDA, SOD, TNF-α, and IL-6 ELISA detection kits were purchased from Nanjing Jiancheng Bioengineering Institute (Nanjing, China).

    Techniques: In Vitro, CCK-8 Assay, Enzyme-linked Immunosorbent Assay, Fluorescence

    Schematic diagram illustrating the mechanism by which HCP alleviates HIRI by regulating macrophage polarization via the TLR4/NF-κB pathway. After three days of intraperitoneal injection pretreatment with HCP, a 70% hepatic ischemia for 1 h followed by 24 h reperfusion injury model was established. HCP inhibits the activation of TLR4 on the surface of hepatic Kupffer cells, and blocks the downstream MyD88-dependent NF-κB signaling pathway, thereby reducing NF-κB nuclear translocation and the release of pro-inflammatory cytokines (TNF-α, IL-6). Concurrently, HCP regulates macrophage phenotypes, suppressing M1 polarization and promoting M2 polarization, ultimately alleviating hepatic ischemia-reperfusion injury.

    Journal: Biomedicines

    Article Title: Houttuynia cordata Polysaccharide Alleviates Hepatic Ischemia-Reperfusion Injury by Regulating Macrophage Polarization via Inhibiting the TLR4/NF-κB Signaling Pathway

    doi: 10.3390/biomedicines14020433

    Figure Lengend Snippet: Schematic diagram illustrating the mechanism by which HCP alleviates HIRI by regulating macrophage polarization via the TLR4/NF-κB pathway. After three days of intraperitoneal injection pretreatment with HCP, a 70% hepatic ischemia for 1 h followed by 24 h reperfusion injury model was established. HCP inhibits the activation of TLR4 on the surface of hepatic Kupffer cells, and blocks the downstream MyD88-dependent NF-κB signaling pathway, thereby reducing NF-κB nuclear translocation and the release of pro-inflammatory cytokines (TNF-α, IL-6). Concurrently, HCP regulates macrophage phenotypes, suppressing M1 polarization and promoting M2 polarization, ultimately alleviating hepatic ischemia-reperfusion injury.

    Article Snippet: Mouse ALT, AST, MDA, SOD, TNF-α, and IL-6 ELISA detection kits were purchased from Nanjing Jiancheng Bioengineering Institute (Nanjing, China).

    Techniques: Injection, Activation Assay, Translocation Assay