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Temporal analysis of the BMSC paracrine profile on different scaffolds. (A) Confocal microscopy images from Live/Dead fluorescence staining of BMSCs encapsulated within the PCL/HAp-GelMA/BMSCs scaffold after 1, 3, 5, and 14 d of 3D culture (live cells, green; dead cells, red). (B) The concentrations of key paracrine <t>factors</t> <t>(TGF-β,</t> PGE2, VEGF, <t>HGF,</t> and BMP-2) from BMSCs cultured in different scaffolds, quantified from culture supernatants at day 3 and day 7. (C) Corresponding relative mRNA expression levels of TGFB1, PTGS2, VEGFA, HGF, and BMP-2 in BMSCs at day 3 and day 7, as determined by qPCR analysis. Data are presented as mean ± SD (n = 3) *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns: not significant.
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CCK-8 value of <t>HGFs</t> of Ag-Est816 and PBS at Day 1, 3 and 7. Ag-Est816, nanocomposite of silver nanoparticles and N -acyl-homoserine lactone-lactonase Est816; CCK-8, cell counting Kit-8; HGFs, human gingival <t>fibroblasts;</t> PBS, phosphate-buffered saline (control), ns, P > .05).
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CCK-8 value of <t>HGFs</t> of Ag-Est816 and PBS at Day 1, 3 and 7. Ag-Est816, nanocomposite of silver nanoparticles and N -acyl-homoserine lactone-lactonase Est816; CCK-8, cell counting Kit-8; HGFs, human gingival <t>fibroblasts;</t> PBS, phosphate-buffered saline (control), ns, P > .05).
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Image Search Results


Temporal analysis of the BMSC paracrine profile on different scaffolds. (A) Confocal microscopy images from Live/Dead fluorescence staining of BMSCs encapsulated within the PCL/HAp-GelMA/BMSCs scaffold after 1, 3, 5, and 14 d of 3D culture (live cells, green; dead cells, red). (B) The concentrations of key paracrine factors (TGF-β, PGE2, VEGF, HGF, and BMP-2) from BMSCs cultured in different scaffolds, quantified from culture supernatants at day 3 and day 7. (C) Corresponding relative mRNA expression levels of TGFB1, PTGS2, VEGFA, HGF, and BMP-2 in BMSCs at day 3 and day 7, as determined by qPCR analysis. Data are presented as mean ± SD (n = 3) *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns: not significant.

Journal: Bioactive Materials

Article Title: Mesenchymal stromal cells-loaded 3D radially aligned composite scaffold with potentiated paracrine signaling for sequential bone regeneration

doi: 10.1016/j.bioactmat.2026.02.059

Figure Lengend Snippet: Temporal analysis of the BMSC paracrine profile on different scaffolds. (A) Confocal microscopy images from Live/Dead fluorescence staining of BMSCs encapsulated within the PCL/HAp-GelMA/BMSCs scaffold after 1, 3, 5, and 14 d of 3D culture (live cells, green; dead cells, red). (B) The concentrations of key paracrine factors (TGF-β, PGE2, VEGF, HGF, and BMP-2) from BMSCs cultured in different scaffolds, quantified from culture supernatants at day 3 and day 7. (C) Corresponding relative mRNA expression levels of TGFB1, PTGS2, VEGFA, HGF, and BMP-2 in BMSCs at day 3 and day 7, as determined by qPCR analysis. Data are presented as mean ± SD (n = 3) *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns: not significant.

Article Snippet: ELISA kits for PGE2 (Cat. No. E-EL-0034), TGF-β (Cat. No. E-EL-0162), VEGF (Cat. No. E-EL-R2603), and HGF (Cat. No. E-EL-R0496) were purchased from Elabscience (Wuhan, China).

Techniques: Confocal Microscopy, Fluorescence, Staining, Cell Culture, Expressing

CCK-8 value of HGFs of Ag-Est816 and PBS at Day 1, 3 and 7. Ag-Est816, nanocomposite of silver nanoparticles and N -acyl-homoserine lactone-lactonase Est816; CCK-8, cell counting Kit-8; HGFs, human gingival fibroblasts; PBS, phosphate-buffered saline (control), ns, P > .05).

Journal: International Dental Journal

Article Title: Developing a Silver Nanocomposite With Quorum-Quenching Enzyme Ag-Est816 to Prevent Periodontitis

doi: 10.1016/j.identj.2026.109481

Figure Lengend Snippet: CCK-8 value of HGFs of Ag-Est816 and PBS at Day 1, 3 and 7. Ag-Est816, nanocomposite of silver nanoparticles and N -acyl-homoserine lactone-lactonase Est816; CCK-8, cell counting Kit-8; HGFs, human gingival fibroblasts; PBS, phosphate-buffered saline (control), ns, P > .05).

Article Snippet: The Est816 was prepared and purified according to our established protocols, and its molecular mass was confirmed by sodium dodecyl sulphate-polyacrylamide gel electrophoresis., , Human gingival fibroblasts (HGFs) (HGF-1, ATCC CRL-2014) were used in the following experiments.

Techniques: CCK-8 Assay, Cell Counting, Saline, Control

Cytocompatibility of HGFs treated with Ag-Est816 nanocomposite and PBS (control) at Day 1, 3 and 7. Ag-Est816, nanocomposite of silver nanoparticles and N -acyl-homoserine lactone-lactonase Est816; PBS, Phosphate-buffered Saline (Control). Immunofluorescence staining: F‑actin labelled the cytoskeleton in red, DAPI labelled nuclei in blue.

Journal: International Dental Journal

Article Title: Developing a Silver Nanocomposite With Quorum-Quenching Enzyme Ag-Est816 to Prevent Periodontitis

doi: 10.1016/j.identj.2026.109481

Figure Lengend Snippet: Cytocompatibility of HGFs treated with Ag-Est816 nanocomposite and PBS (control) at Day 1, 3 and 7. Ag-Est816, nanocomposite of silver nanoparticles and N -acyl-homoserine lactone-lactonase Est816; PBS, Phosphate-buffered Saline (Control). Immunofluorescence staining: F‑actin labelled the cytoskeleton in red, DAPI labelled nuclei in blue.

Article Snippet: The Est816 was prepared and purified according to our established protocols, and its molecular mass was confirmed by sodium dodecyl sulphate-polyacrylamide gel electrophoresis., , Human gingival fibroblasts (HGFs) (HGF-1, ATCC CRL-2014) were used in the following experiments.

Techniques: Control, Saline, Immunofluorescence, Staining