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Journal: International Journal of Molecular Medicine
Article Title: Triptolide exerts antiviral effects and alleviates influenza A-induced pneumonia by inhibiting the overactivation of absent in melanoma 2 signaling in immune cells
doi: 10.3892/ijmm.2026.5829
Figure Lengend Snippet: H1N1 infection affects cell viability, inflammatory cytokine secretion and interactions between HBEpiCs and THP-1 cells. (A) CCK-8 assay revealed that HBEpiC viability decreased in a concentration-dependent manner following H1N1 infection. (B) ELISA revealed that the levels of IL-1β, IL-6, TNF-α, and IL-8 in HBEpiCs decreased with increasing H1N1 infection. (C) CCK-8 assay indicated that supernatants from H1N1-infected HBEpiC cultures reduced the viability of THP-1 cells in a dose-dependent manner. (D) ELISA results suggested that the levels of inflammatory cytokines (IL-1β, IL-6, TNF-α and IL-8) in THP-1 cells were decreased following exposure to supernatants from H1N1-infected HBEpiC cultures. (E) Cell adhesion assay revealed that the number of THP-1 cells adhering to HBEpiCs increased with increasing H1N1 concentration (scale bar, 10 μ m). Arrow indicates THP-1 cells that remain attached to the surface of HBEpiCs, highlighting the adhesion interaction between the two cell types. (F) Transwell assay suggested that H1N1 infection enhanced the migration capacity of THP-1 cells, with increased migration observed at higher virus concentrations (scale bar, 50 μ m). The data are presented as the mean ± standard deviation; ** P<0.01, *** P<0.001 vs. control. H1N1, influenza A; HBEpiCs, human bronchial epithelial cells; ELISA, enzyme-linked immunosorbent assay; IL, interleukin; TNF-α, tumor necrosis factor-α; Con, control; MOI, multiplicity of infection.
Article Snippet: Cell supernatants were collected and analyzed using
Techniques: Infection, CCK-8 Assay, Concentration Assay, Enzyme-linked Immunosorbent Assay, Cell Adhesion Assay, Transwell Assay, Migration, Virus, Standard Deviation, Control
Journal: International Journal of Molecular Medicine
Article Title: Triptolide exerts antiviral effects and alleviates influenza A-induced pneumonia by inhibiting the overactivation of absent in melanoma 2 signaling in immune cells
doi: 10.3892/ijmm.2026.5829
Figure Lengend Snippet: TP modulates the inflammatory response and immune cell activity in H1N1-infected HBEpiCs and THP-1 cells. (A) No significant changes were observed in HBEpiCs treated with various concentrations of TP (5, 10 and 20 nM) following H1N1 infection compared with the control. (B) After TP treatment, the levels of the inflammatory cytokines IL-1β, IL-6, TNF-α and IL-8 in HBEpiCs were markedly lower than those in the untreated group. (C) The viability of THP-1 cells pretreated with H1N1-infected HBEpiC culture supernatant decreased after TP treatment. (D) The levels of IL-1β, IL-6, TNF-α, and IL-8 in THP-1 cells were markedly lower after TP treatment. (E) The adhesion of THP-1 cells to HBEpiCs induced by H1N1 infection decreased in a dose-dependent manner with increasing TP concentration (scale bar, 10 μ m). Arrow indicates THP-1 cells that remain attached to the surface of HBEpiCs, highlighting the adhesion interaction between the two cell types. (F) The migration capacity of THP-1 cells was markedly reduced when the supernatant from H1N1-infected HBEpiC cultures was treated with TP (scale bar, 50 μ m). The data are presented as the mean ± standard deviation; * P<0.05, ** P<0.01, *** P<0.001 vs. control. TP, triptolide; H1N1, influenza A; HBEpiCs, human bronchial epithelial cells; IL, interleukin; TNF-α, tumor necrosis factor-α; Con, control.
Article Snippet: Cell supernatants were collected and analyzed using
Techniques: Activity Assay, Infection, Control, Concentration Assay, Migration, Standard Deviation
Journal: International Journal of Molecular Medicine
Article Title: Triptolide exerts antiviral effects and alleviates influenza A-induced pneumonia by inhibiting the overactivation of absent in melanoma 2 signaling in immune cells
doi: 10.3892/ijmm.2026.5829
Figure Lengend Snippet: AIM2 overexpression reverses the immunosuppressive effects of TP in THP-1 cells. (A) Transfection with Ad-AIM2 upregulated the expression of AIM2 compared with that of Ad-NC in THP-1 cells. (B) AIM2 protein levels were elevated in THP-1 cells overexpressing AIM2 compared with control THP-1 cells. (C) In THP-1 cells, AIM2 overexpression increased the LDH leakage rate. (D) AIM2 overexpression reversed the TP-induced reduction in adhesion between THP-1 cells and HBEpiCs (scale bar, 10 μ m). (E) AIM2 overexpression enhanced the migration ability of THP-1 cells compared with that of H1N1-treated control cells and reversed the TP-induced decrease in THP-1 cell migration (scale bar, 50 μ m). (F) AIM2 overexpression reversed the TP-induced reduction in inflammatory cytokine levels. The data are presented as the mean ± standard deviation; * P<0.05, ** P<0.01, *** P<0.001 vs. Con; # P<0.05, ## P<0.01, ### P<0.001 vs. Ad-AIM2. AIM2, absent in melanoma 2; TP, triptolide; LDH, lactate dehydrogenase; HBEpiCs, human bronchial epithelial cells; H1N1, influenza A; GSDMD, gasdermin D; IL, interleukin; TNF-α, tumor necrosis factor-α; Con, control.
Article Snippet: Cell supernatants were collected and analyzed using
Techniques: Over Expression, Transfection, Expressing, Control, Migration, Standard Deviation
Journal: Cancer Immunology, Immunotherapy : CII
Article Title: KSR2 functions as a metabolic checkpoint for anti-PD-1 resistance by reprogramming glucose metabolism
doi: 10.1007/s00262-026-04394-z
Figure Lengend Snippet: KSR2 overexpression associated with an immunosuppressive tumor microenvironment. A Flow cytometry analysis of tumor-infiltrating CD4⁺ T, CD8⁺ T, and regulatory T cells ( n = 3 mice). B , C ELISA quantification of GzmB ( B ) and IFN-γ ( C ) levels ( n = 3 mice). D MIF analysis (CD8, red; GzmB, green; Treg, yellow; DAPI, blue) and cell quantification (3 fields/sample; n = 3 mice). Mean ± SD. two-tailed unpaired t test or Welch’s t test (* P < 0.05, ** P < 0.01, *** P < 0.001)
Article Snippet: Mouse tumor homogenates were prepared, and concentrations of granzyme B and IFN-γ were measured using the mouse granzyme B ELISA kit (E-EL-M0594, Elabscience) and
Techniques: Over Expression, Flow Cytometry, Enzyme-linked Immunosorbent Assay, Two Tailed Test
Journal: Cancer Immunology, Immunotherapy : CII
Article Title: KSR2 functions as a metabolic checkpoint for anti-PD-1 resistance by reprogramming glucose metabolism
doi: 10.1007/s00262-026-04394-z
Figure Lengend Snippet: KSR2 knockdown reverses metabolic reprogramming and reinstates anti-tumor immunity. A Differential metabolite abundance in control versus Ksr2-knockdown tumors ( n = 3 mice). B IHC analysis of LDHA and HK2 expression. 3 fields/sample; n = 3 mice. Scale bars, 100μm, 20 μ m. C , D GzmB ( C ) and IFN-γ ( D ) levels in tumors by ELISA ( n = 3). E MIF analysis and cell quantification (3 fields/sample; n = 3 mice). Mean ± SD. Two-tailed unpaired t test or Welch’s t test (* P < 0.05, ** P < 0.01, *** P < 0.001)
Article Snippet: Mouse tumor homogenates were prepared, and concentrations of granzyme B and IFN-γ were measured using the mouse granzyme B ELISA kit (E-EL-M0594, Elabscience) and
Techniques: Knockdown, Control, Expressing, Enzyme-linked Immunosorbent Assay, Two Tailed Test