1C–E). The cortex of the adrenal gland also showed prominent hybridization of the three cortical zones with no expression seen in the medulla http://www.selleckchem.com/products/BAY-73-4506.html (Fig. 1F and G). In the kidney a high level of APJ expression was seen in the medulla, specifically the inner stripe of the outer medulla, consistent with hybridization to the medullary rays, with patch-like labeling observed in the outer cortex that may correspond to tubular structures

(e.g. distal/proximal tubule) (Fig. 2A). No labeling was seen in the glomeruli. In the lung, APJ mRNA was restricted to the parenchyma (Fig. 2B) and there was no evidence of any association with the lining of blood vessels or in the bronchi or bronchioles. In the pyloric region of the stomach the mucosal layer of the stomach lining showed a strong hybridization signal for APJ (Fig. 2C) with transcript also seen within the villi of the ileum (Fig. 2D). Hybridization within the heart was widespread with

APJ expression present in cardiomyocytes throughout the myocardium PD-L1 inhibitor (Fig. 2E). No signal was observed in heart sections hybridized with sense probe (inset), similarly no APJ mRNA signal was detected in heart tissue from APJ KO mice (Fig. 2F). Moderate hybridization levels were present in the uterine endometrial lining, however no signal was detected in the myometrium (Fig. 3A). In the ovary (Fig. 3B), the theca cells surrounding the antral follicles showed intense labeling (Fig. 3B and C) as did the cells of

the corpus luteum (Fig. 3B), while no signal was present in ovary sections hybridized with sense probe (Fig. 3B, inset) and only background levels of radiolabeling were FAD detected in the ovary of APJ KO mice (Fig. 3D). APJ mRNA, as indicated by the presence of hybridization signal, was not detected in a number of other tissues including liver, spleen, gall bladder, thymus, trachea, pancreas and testis (images not shown). The pattern of APJ mRNA expression was similar between male and female mice. The data is summarized in Table 1. [125I]-(Pyr1)apelin-13 was used to localize APJ binding sites in the mouse brain and peripheral tissues. Binding specificity was assessed by binding of radiolabeled apelin-13 in the presence of 1 μM unlabeled (Pyr1)apelin-13 and by comparison of APJ distribution in wildtype mouse tissue to that in APJ KO tissues, where no specific binding was observed in any tissue. Of note, while APJ binding corresponds to correctly processed and folded receptors it does not unquestionably infer that the receptors present are capable of signaling.