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Journal: Drug Design, Development and Therapy
Article Title: (+)-JQ1 Upregulates SIRT3 to Suppress cGAS/STING Pathway-Mediated Neuronal Inflammation and Ferroptosis After Hypoxic-Ischemic Encephalopathy
doi: 10.2147/DDDT.S578815
Figure Lengend Snippet: SIRT3 Mediates the Protective Effects of JQ1 Against CGAS/STING Activation and Ferroptosis Following OGD. ( A ) Representative Western blot images of SIRT3, cGAS, and STING expression in HT22 cells. ( B ) Representative images of immunofluorescence staining for STING (green) and DAPI (blue) in HT22 cells of each group. Scale bar = 25μm. ( C ) Representative images of immunofluorescence staining for cGAS (green) and DAPI (blue) in HT22 cells of each group. Scale bar = 25μm. ( D – G ) Representative Western blot images and quantification of SLC3A2, SLC7A11, and GPX4 expression (normalized to β-Actin) in HT22 cells. ( H – K ) Representative Western blot images and quantification of STING, SLC7A11, and GPX4 expression (normalized to β-Actin) in HT22 cells. Data are expressed as mean ± SD independent replicates: ns: not significant; ###P < 0.001 versus Control group; *P < 0.05, **P < 0.01, ***P < 0.001 versus OGD+JQ1+si-NC group; @P < 0.05, @@P < 0.01, @@@P < 0.001 versus OGD +C-176 group; &P < 0.05 versus OGD+JQ1 group.
Article Snippet: To inhibit STING, the cells were pre-stimulated with 1 μM
Techniques: Activation Assay, Western Blot, Expressing, Immunofluorescence, Staining, Control