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Image Search Results
Journal: Clinical and Experimental Pharmacology & Physiology
Article Title: Mechanisms of IL‐17A Neutralisation in Alleviating Renal Fibrosis and Inflammation in Spontaneously Hypertensive Rats
doi: 10.1111/1440-1681.70116
Figure Lengend Snippet: Effects of IL‐17A neutralisation on macrophage polarisation in SHR renal tissues. (A) Representative IHC staining of M1 macrophage markers (iNOS and CD86) with quantitative analysis of their positive areas. (B) Representative IHC staining of M2 macrophage markers (Arg‐1 and CD163) with quantitative analysis of their positive areas. (C) Representative immunoblots and relative expression levels of iNOS, CD86, Arg‐1, and CD163 proteins. (D) Proportion of CD86 + and CD163 + cells among CD68 + macrophages. (E) mRNA expression levels of iNOS, CD86, Arg‐1, and CD163. Data are presented as mean ± SD ( n = 6).
Article Snippet: Sections were then incubated overnight at 4°C with primary antibodies against: E‐cadherin (Boster, China), Collagen III (Boster, China),
Techniques: Immunohistochemistry, Western Blot, Expressing
Journal: Neurochemistry international
Article Title: Cannabinoid-profiled agents improve cell survival via reduction of oxidative stress and inflammation, and Nrf2 activation in a toxic model combining hyperglycemia+Aβ 1-42 peptide in rat hippocampal neurons.
doi: 10.1016/j.neuint.2020.104817
Figure Lengend Snippet: Fig. 13. Effects of increased concentrations (1–1000 nM, for 6 h) of anandamide (AEA), 2-arachidonoylglycerol (2-AG), CP 55–940, WIN 55,212–2, and URB597, on inducible-nitric oxide synthase (iNOS; A), Interleukin-1β (IL-1β; B), and Tumor Necrosis Factor-α (TNF-α; C) levels in primary hippocampal neurons exposed to high glucose (GLU; 150 mM for 48 h) + amyloid β peptide (Aβ1-42; 500 nM for 24 h). Data are mean values ± S.E.M. of n = 2 experiments per assay. **P ≤0.01 and ʄP ≤ 0.001, different from the control group; +P ≤0.05, ++P ≤0.01 and ɸP ≤0.001, different from the GLU + Aβ1-42 group; Kruskal-Wallis ANOVA with uncorrected Dunn’s test.
Article Snippet:
Techniques: Control
Journal: Human Cell
Article Title: Single-cell dynamic RNA and glycosylation sequencing reveals the mechanism underlying the differentiation of pluripotent stem cells into hematopoietic stem cells
doi: 10.1007/s13577-025-01234-7
Figure Lengend Snippet: The analysis for the heterogeneity of endothelial clusters. a . The gene expression of endothelial, angiogenesis, and hematopoiesis in new RNA. b . The hotspot analyzed the similarity of cells and obtained 12 modules. c–d . The vascular endothelial cell migration pathway was selected from modules 3 and 8 and mapped to UMAP plots. e . The GO analysis of differential genes in high-glucose and low-glucose cells. f . The endothelial and hematopoietic genes in high-glucose and low-glucose cells in clusters 1 and 15
Article Snippet: From day 2 to day 6, 50 ng/mL
Techniques: Gene Expression, Migration
Journal: Human Cell
Article Title: Single-cell dynamic RNA and glycosylation sequencing reveals the mechanism underlying the differentiation of pluripotent stem cells into hematopoietic stem cells
doi: 10.1007/s13577-025-01234-7
Figure Lengend Snippet: Potential linkages of endothelial subsets in their differentiation fate. a . Clusters 1 and 15 were reclustered to seven new clusters, which were identified by differentially expressed genes, including NEFH, CLDN5, TOP2 A, RUNX1, MCM3, ANGPT2, and IGFBP3. b . The expression of endothelial and hematopoietic-related genes in endothelial subsets. c–d . The NTR and the levels of glycation in endothelial subsets. e . The expression of transcription factors in the endothelial subsets. f . The correlation between clusters 1, 15, and the endothelial subsets using the Spearman correlation analysis
Article Snippet: From day 2 to day 6, 50 ng/mL
Techniques: Expressing