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. 2017 May 15;7:1885. doi: 10.1038/s41598-017-01764-7

Figure 1.

Figure 1

Integrin beta8 regulates the activity of FAK in the endometrial epithelial cells during their receptivity. (A) Integrin beta8 expression analysis was performed on the endometrial epithelial cells with the help of immunoblotting and densitometry. (B) Employing immunofluroescence, the localization of integrin beta8 was performed through confocal laser scanning microscope in the endometrial epithelial cells of mouse origin. (C) Silencing of Itgb8 from endometrial epithelial cells was confirmed by immunoblotting and densitometry. (D) The expression level of phosphorylated and total forms of FAK was examined in response to Itgb8 silencing in the endometrial epithelial cells using immunoblotting and densitometry. (E,F) Similarly, FAK activity was determined by way of phosphorylation (Y-397) level determination by ELISA in the endometrial tissue protein extract from day5, 1000 h stage post-Itgb8 silencing at day4, 1000 h. Actin beta was used as the loading control to normalize the western blot values. (**p < 0.01,*p < 0.05, NS p > 0.05). Magnification of the image was at 63X and 189X. Scale bar; 20 and 5 µm respectively.