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Journal: Biochemistry and Biophysics Reports
Article Title: TMEM207-mediated the impairment of skin regeneration through YAP sequestration in an allergic contact dermatitis model
doi: 10.1016/j.bbrep.2025.102409
Figure Lengend Snippet: (A): (left) Representative immunohistochemical staining of the skin using an anti -ABCB1 antibody. (center) Comparison of PPARg and SCD1 gene expression. (right) Representative immunohistochemical staining of the skin using an anti -SCD1 antibody. ∗∗ no significant difference; ∗P < 0.05. (B): Representative immunohistochemical staining of the skin using an anti -ki67 antibody and Nuclear Ki67 IHC score. Expression of ki67 was significantly reduced in Tg compared to wild type. ∗P < 0.05. (C): Representative immunohistochemical staining of the skin using an anti -Loricrin antibody. (D): Representative immunohistochemical staining of the skin using an anti-YAP antibody.
Article Snippet: Rabbit anti -GAPDH antibodies were obtained from Sigma-Aldrich (St. Louis, MO, USA), and rabbit anti -ABCB1, anti -
Techniques: Immunohistochemical staining, Staining, Comparison, Gene Expression, Expressing
Journal: iScience
Article Title: Roseburia hominis enriched by baicalin reverses the non-response to metformin via upregulating linolenic acid metabolism
doi: 10.1016/j.isci.2025.113892
Figure Lengend Snippet: R. hominis intervention promoted LA metabolism in mice, and its effect on reversing the NR in mice depended on PLA2 (A) The PCA score plot in negative and positive ion modes. In the negative ion mode, the prediction rate (Q2) of the PCA-X model is 0.599, and the interpretation rate (R2X) is 0.771. The prediction rate (Q2) of the PCA-X model in positive ion mode is 0.487, and the interpretation rate (R2X) is 0.712. (B) Enrichment analysis of differential metabolites. (C–E) The serum abundance of (C) PC (18:3/16:0), (D) LA, and (E) SDA. (F) Schematic diagram of LA metabolism. The blue background represents metabolites, while the green background represents enzymes. The red font represents the substances detected in the study. (G) Western blot analysis of PLA2G and FADS2 proteins in the livers of mice after R. hominis administration. (H) The activity of PLA2 after darapladib intervention. (I) Oral glucose tolerance test (OGTT) curve and its area under the curve (AUC). (J) Insulin tolerance test (ITT) curve and its AUC. (K) Homeostatic model assessment for insulin resistance (HOMA-IR) after drug administration. Data are expressed as the mean ± SD ( n = 7–8); ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, as determined by one-way ANOVA with Holm-Sidak’s post hoc test. ANOVA, analysis of variance; PC, phosphatidylcholine; NR, non-response; NCD, normal chow diet; R.h, Roseburia hominis ; PLA2, phospholipase A2; FADS2, fatty acid desaturase 2; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; PCA, principal-component analysis.
Article Snippet: These membranes were then incubated at 4°C overnight with primary antibodies against AMP-activated protein kinase (AMPK) (Proteintech, Cat# 10929-2-AP, RRID: AB_2169568 , 1:4,000), insulin receptor substrate 1 (IRS1) (Proteintech, Cat# 17509-1-AP, RRID: AB_10596914 , 1:1,000), phospho-AMPKα (Thr172) (40H9) (Cell Signaling Technology, Cat# 2535, RRID: AB_331250 , 1:1,000), phospho-IRS-1 (Ser636/639) (Cell Signaling Technology, Cat# 2388, RRID: AB_330339 , 1:1,000), phosphoenolpyruvate carboxykinase (PCK) (Proteintech, Cat# 16754-1-AP, RRID: AB_2160031 , 1:30,000), glucose-6-phosphatase (G6PC) (Proteintech, Cat# 66860-1-Ig, RRID: AB_2882199 , 1:5,000), mammalian target of rapamycin (mTOR) (Proteintech, Cat# 66888-1-Ig, RRID: AB_2882219 , 1:30,000),
Techniques: Western Blot, Activity Assay