Journal of Traditional Chinese Medicine ›› 2025, Vol. 45 ›› Issue (6): 1317-1329.DOI: 10.19852/j.cnki.jtcm.2025.06.011
• Original Articles • Previous Articles Next Articles
LI Keyao1, SHU Ye2, CHANG Jing2, TANG Jianping2, ZHANG Litao3(
), WEI Zhu4(
)
Received:2025-09-12
Accepted:2025-01-26
Online:2025-12-15
Published:2025-11-24
Contact:
ZHANG Litao, Tianjin Medical University, Affiliated Hospital of Tianjin Academy of Traditional Chinese Medicine, Tianjin 300193, China. zhanglitao@medmail.com.cn, Telephone: +86-13467622617;Supported by:LI Keyao, SHU Ye, CHANG Jing, TANG Jianping, ZHANG Litao, WEI Zhu. Psoriasis intervention by Huai’er (Trametes): unveiling novel targets via network pharmacology[J]. Journal of Traditional Chinese Medicine, 2025, 45(6): 1317-1329.
Figure 1 Investigation of the effects of Huai'er (Trametes) on HaCaT cell behavior A: bright-field/phase-contrast image of HaCaT cells without staining. Scale bar = 50 μm; B: CCK-8 cell viability of HaCaT cells treated with Huai'er (Trametes) at 0, 2, 4, 8, and 16 mg/mL for 24, 48, and 72 h. Two-way ANOVA (factors: concentration and time) was performed with post-hoc tests when appropriate; C: EdU fluorescence staining of HaCaT cells treated with 8 mg/mL Huai'er (Trametes) for different time points.C1: 0 h; C2: 12 h; C3: 24 h; C4: 48 h. EdU? cells are shown in red; nuclei are stained with DAPI (blue). Scale bar = 50 μm.); D: percentage of EdU? cells in different time groups (0, 12, 24, 48 h). AEdU: 5-ethynyl-2′-deoxyuridine; DAPI: 4′, 6-diamidino-2-phenylindole; CCK-8: cell counting kit-8; ANOVA: analysis of variance. Data are presented as mean ± standard deviation (n = 3). One-way ANOVA was used for statistical analysis. Compared with the 0 h group, aP < 0.01.
Figure 2 Investigation of the effects of Huai'er (Trametes) on HaCaT cell behavior and expression of inflammatory factors A: scratch-wound assay of HaCaT cells imaged by phase-contrast microscopy (no staining); a 100 μm scale bar is shown at the bottom right of each image. A1-A4: representative images of Control and Huai'er (Trametes) at 0 h and 24 h (A1: Control group at 0 h; A2: Huai’er (Trametes) group at 0 h; A3: Control group at 24 h; A4: Huai’er (Trametes) group at 24 h); A5: quantification of migration distance (%); B: RT-qPCR analysis of inflammatory cytokine mRNA levels. B1: IL-6; B2: IL-8; B3: IL-10; B4: IL-23; B5: IL-17; B6: TNF-α. The cell experiments mentioned above were repeated three times. Control: untreated; Huai'er (Trametes): treated with Huai'er (Trametes) at 8 mg/mL for 24 h; scratch assay time points: 0 h and 24 h. RT-qPCR: reverse transcription quantitative polymerase chain reaction; IL: interleukin; TNF-α: tumor necrosis factor alpha; ANOVA: analysis of variance. Data are presented as mean ± standard deviation (n = 3). Two-group comparisons used a two-tailed unpaired t-test (or one-way ANOVA with post-hoc tests, keep consistent with your methods). Compared to the Control group, aP < 0.01.
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