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Characterization of the uterus tissue with SPCM treatment. <t>a,</t> <t>α-SMA</t> staining gauged smooth-muscle thickness. Scale bars, 100 μm. (The white line indicates smooth muscle thickness). b-c, <t>VEGF/MVD</t> immunofluorescence (200 μm) mapped blood vessels. Scale bars, 200 μm. d-e, IL-10 and IL-6 staining quantified local inflammation. Scale bars, 200 μm. g-i, Quantitative analysis of the molecular expression levels mentioned above in the uterus tissues. ∗ P < 0.05 for One Way ANOVA.
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Characterization of the uterus tissue with SPCM treatment. <t>a,</t> <t>α-SMA</t> staining gauged smooth-muscle thickness. Scale bars, 100 μm. (The white line indicates smooth muscle thickness). b-c, <t>VEGF/MVD</t> immunofluorescence (200 μm) mapped blood vessels. Scale bars, 200 μm. d-e, IL-10 and IL-6 staining quantified local inflammation. Scale bars, 200 μm. g-i, Quantitative analysis of the molecular expression levels mentioned above in the uterus tissues. ∗ P < 0.05 for One Way ANOVA.
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Characterization of the uterus tissue with SPCM treatment. <t>a,</t> <t>α-SMA</t> staining gauged smooth-muscle thickness. Scale bars, 100 μm. (The white line indicates smooth muscle thickness). b-c, <t>VEGF/MVD</t> immunofluorescence (200 μm) mapped blood vessels. Scale bars, 200 μm. d-e, IL-10 and IL-6 staining quantified local inflammation. Scale bars, 200 μm. g-i, Quantitative analysis of the molecular expression levels mentioned above in the uterus tissues. ∗ P < 0.05 for One Way ANOVA.
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Characterization of the uterus tissue with SPCM treatment. <t>a,</t> <t>α-SMA</t> staining gauged smooth-muscle thickness. Scale bars, 100 μm. (The white line indicates smooth muscle thickness). b-c, <t>VEGF/MVD</t> immunofluorescence (200 μm) mapped blood vessels. Scale bars, 200 μm. d-e, IL-10 and IL-6 staining quantified local inflammation. Scale bars, 200 μm. g-i, Quantitative analysis of the molecular expression levels mentioned above in the uterus tissues. ∗ P < 0.05 for One Way ANOVA.
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Characterization of the uterus tissue with SPCM treatment. a, α-SMA staining gauged smooth-muscle thickness. Scale bars, 100 μm. (The white line indicates smooth muscle thickness). b-c, VEGF/MVD immunofluorescence (200 μm) mapped blood vessels. Scale bars, 200 μm. d-e, IL-10 and IL-6 staining quantified local inflammation. Scale bars, 200 μm. g-i, Quantitative analysis of the molecular expression levels mentioned above in the uterus tissues. ∗ P < 0.05 for One Way ANOVA.

Journal: Materials Today Bio

Article Title: Spatiotemporal piezoelectric microspheres for wireless endometrial repair with improved pregnancy outcomes

doi: 10.1016/j.mtbio.2026.102915

Figure Lengend Snippet: Characterization of the uterus tissue with SPCM treatment. a, α-SMA staining gauged smooth-muscle thickness. Scale bars, 100 μm. (The white line indicates smooth muscle thickness). b-c, VEGF/MVD immunofluorescence (200 μm) mapped blood vessels. Scale bars, 200 μm. d-e, IL-10 and IL-6 staining quantified local inflammation. Scale bars, 200 μm. g-i, Quantitative analysis of the molecular expression levels mentioned above in the uterus tissues. ∗ P < 0.05 for One Way ANOVA.

Article Snippet: Acteoside (CAS:61276-17-3) was bought from Shanghai Yuanye Bio-Technology Co., Ltd. Lipopolysaccharide (LPS) was bought from Beijing Solarbio Science & Technology Co., Ltd (Beijing, China). α-SMA, MVD, VEGF, IL-6, IL-10 antibodies for rat were manufactured by Proteintech Group, Inc. (Chicago, USA).

Techniques: Staining, Immunofluorescence, Expressing