BPG is committed to discovery and dissemination of knowledge
Basic Study
©Author(s) (or their employer(s)) 2026.
World J Stem Cells. Feb 26, 2026; 18(2): 114032
Published online Feb 26, 2026. doi: 10.4252/wjsc.v18.i2.114032
Figure 2
Figure 2 Knockdown of epidermal growth factor receptor blocked the positive effects of epiregulin on migration, chemotaxis, and osteogenic potential of mouse bone marrow stem cells under inflammatory conditions. A: Quantitative analysis of quantitative real-time polymerase chain reaction showed that the transcription of epidermal growth factor receptor (Egfr) mRNA was decreased in the EGFR single hairpin RNA (shRNA) group (n = 3, Student’s t-test). Glyceraldehyde 3-phosphate dehydrogenase (Gapdh) was used as an internal control; B: Expression of EGFR was revealed in mouse bone marrow stem cells by western blotting. GAPDH was used as the internal control; C and D: Scratch-simulated wound migration assay results (n = 3, one-way analysis of variance [ANOVA]). Scale bar: 500 μm; E and F: Transwell chemotaxis assay results (n = 3, one-way ANOVA). Scale bar: 50 μm; G: Alizarin Red staining; H: Expression of osterix (OSX) and osteocalcin (OCN) was revealed in mouse bone marrow stem cells that were cultured in the inflammatory condition by western blotting. Error bars represent standard deviation. aP ≤ 0.05; bP ≤ 0.01. EREG: Epiregulin.


Write to the Help Desk