Immunohistochemical staining revealed that OCT2, OCT3, MATE1, and MATE2 were present in membrane and cytoplasm of both the epithelial and stromal

cells of the human endometrium (Figure 1 B1–E1). One interesting observation from the immunohistochemical analysis was that OCT1 was absent in epithelial cells and was only expressed in the https://www.selleckchem.com/products/salubrinal.html stromal cells in human endometrium (Figure 1 A1). Furthermore, in the rat uterus we observed that OCT1, OCT2, OCT3, and MATE1 were strongly expressed in luminal and glandular epithelial cells and less strongly in stromal cells (Figure 1 A2–D2). Western blot analysis confirmed the expression of OCT1, OCT2, OCT3, and MATE1 in the rat uterus (Figure 1 E2). Because specific OCTs and MATEs contribute to the effects

Combretastatin A4 cost of metformin in different tissues such as liver and kidney [66], buy SAHA HDAC these findings support the hypothesis that metformin could have a direct effect on the endometrium in women with PCOS that is dependent on OCTs. If proven correct, this hypothesis will not only provide an explanation for the results of our clinical study [49], but will also provide a novel therapeutic option for women who might develop endometrial atypical hyperplasia and EC even in the absence of PCOS. Figure 1 Comparison of endogenous OCT1, OCT2, OCT3, MATE1, and MATE2 localization in human endometria and rat uterine tissues. Human endometrial biopsies (n = 4) and rat uteri (n = 6) were

fixed in formalin and embedded in paraffin. Rabbit anti-OCT1 (AV41516, 1:100 dilution Resminostat for human and rat), rabbit anti-OCT2 (HPA008567, 1:100 for human, 1:200 for rat), and rabbit anti-MATE1 (HPA021987, 1:100 for human, 1:200 for rat) were obtained from Sigma-Aldrich (Saint Louis, MO, USA). Rabbit anti-OCT3 (ab183071, 1:25 for human, 1:100 for rat) and rabbit anti-MATE2 (ab106117, 1:100 for human) were obtained from Abcam (Cambridge, UK). The localization of OCT1–3 and MATE1 and 2 was observed with a peroxidase-antiperoxidase detection method using a single 3,3′-diaminobenzidine (DAB) as the chromogen. Non-specific binding was blocked with Background Sniper (Biocare Medical, CA, USA). Representative micrographs show strong OCT1 immunoreactivity in stromal cells but not in epithelial cells in human endometria (A1). In contrast, OCT1 immunoreactivity is detected in both epithelial and stromal cells in the rat uterus, and there is greater OCT1 immunoreactivity in the epithelial cells (A2). Representative micrographs show that immunoreactivity of OCT2, OCT3, MATE1, and MATE2 is detected in the epithelial and stromal cells in human endometria (B1–E1) and the rat uterus (B2–D2). An antibody against rat MATE2 is not commercially available so this was not tested. Immunofluorescent images of OCT1 are shown in the upper right corner of A1 and A2 and were used to confirm the immunohistochemical analysis.