Journal: Redox Biology
Article Title: Lactate-driven ATP6V1B2 lactylation triggers asthmatic inflammation by linking lysosomal dysfunction to mitochondrial ROS-dependent pyroptosis
doi: 10.1016/j.redox.2026.104059
Figure Lengend Snippet: Effect of blocking ATP6V1B2 lactylation on mouse asthma phenotypes and in vivo pyroptosis signals. (A) H&E and PAS staining and scoring of AAV-transduced mouse lung tissues. (B) Flow cytometric analysis of eosinophils (CD11C − CD45.2 + Siglec-F + ) in BALF. (C) Detection of serum total IgE and HDM-specific IgE levels. (D) ELISA analysis of Th2 cytokines (IL-4, IL-5, IL-13) in BALF. (E) Measurement of lactate levels in serum and lung tissue homogenates. (F) Immunofluorescence staining of in situ Pan-Kla (green) and LAMP1 (red) in lung tissue frozen sections. Scale bar: 100 μm. (G) Immunoblot analysis of GSDME and Caspase-3 cleavage in lung tissue. (H) Lung tissue LDH activity detection. Data are expressed as Mean ± SEM. n = 10 per group. ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001, ∗∗∗∗P < 0.0001; ns, not significant.
Article Snippet: Mouse serum total IgE and HDM-specific IgE (R&D Systems), as well as IL-4 (E-EL-M0043), IL-5 (E-EL-M0722), IL-13 (E-EL-M0727), HMGB1 (E-EL-M0676/E-EL-H1554), IL-1β (E-EL-H0149), and IL-18 (E-EL-H0253) in BALF or cell supernatants were all detected using ELISA kits from Elabscience.
Techniques: Blocking Assay, In Vivo, Staining, Enzyme-linked Immunosorbent Assay, Immunofluorescence, In Situ, Western Blot, Activity Assay