Figure 1.
Embryo-derived chemokine CXCL12 and its receptor endometrial CXCR4/CXCR7. (A) CXCL12 levels were quantified in embryo culture or empty medium by ELISA. Comparison groups are from 3 independent experiments and analyzed using the unpaired Student t test for parametric distributions including p-values (***< 0.001). (B) A schematic diagram of co-culture system of mouse embryo with Ishikawa cells on Matrigel-coated coverslip. (C) Immunofluorescence (IF) staining images (1–5) were obtained from 5 different regions (illustrated on a diagram of (B:1–5)) of coverslip and mouse embryo (white arrow) was attached in the region number 3 (illustrated on a diagram of (B), marked as red spot). Red: CXCR4, Blue: DAPI. Scale Bar; 50 μm. Intensity of CXCR4 in each image was profiled. Images were captured at a magnification of 10 ×. IF staining of CXCR4, CXCR7 (D) and integrin ⍺vβ3, HIF1⍺ (E) in Ishikawa cells in response to CXCL12. Saline-treated cells were used for control. Scale Bar; 20 μm. Intensity of IF staining was quantified using Image J and displayed in graphs. Data are from 4 independent experiments, and analyzed using unpaired Student t test analysis including p-values (*< 0.05, **< 0.01, ***< 0.001, NS; not significant).