Coexpression of adrenomedullin and its receptor component proteins in the reproductive system of the rat during gestation
© Li et al; licensee BioMed Central Ltd. 2010
Received: 29 June 2010
Accepted: 29 October 2010
Published: 29 October 2010
Adrenomedullin (ADM), a novel vasorelaxant peptide, was found in human/rat ovaries and uteri. Plasma ADM level increases in pregnant women and pregnant rats.
The gene expression levels of Adm and its receptor components - Crlr, Ramp1, Ramp2 and Ramp3, the ADM peptide concentration and localization in the rat female reproductive system during gestation were studied by real-time RT-PCR, EIA and immunohistochemical techniques.
The mRNAs of Adm and its receptor component and ADM were differentially distributed between implantation sites and inter-implantation sites of the pregnant uterus. The day on which vaginal sperm were found was taken to be pregnancy day 1. The Adm mRNA levels in the implantation sites of the uteri in mid- (day 12) and late pregnancy (day 17) were more than 10-fold higher than those in nonpregnancy, pre-implantation (day 3) or early (day 7) pregnancy. ADM was localized in the endometrial stroma with increased immunoreactivity from nonpregnancy to pregnancy. The ADM level and the mRNA levels of Adm, Crlr, Ramp2 and Ramp3 in the corpus luteum all increased in late pregnancy compared with early pregnancy. The gene expression of Adm and it receptor components and intense immunostaining of ADM were also found in the oviduct during pregnancy.
The gene expressions levels of Adm and its receptor components - Crlr, Ramp1, Ramp2 and Ramp3, and ADM peptide concentration exhibited a spatio-temporal pattern in the rat female reproductive system during gestation and this suggests that ADM may play important roles in gestation.
Adrenomedullin (ADM) was a novel potent vasodilator first discovered in human pheochromatocytoma tissue in 1993 . The Adm gene and its protein product are highly conserved across species, including human, rat, pig and cow [2–5]. It is a member of the calcitonin family with a high sequence homology to calcitonin gene-related peptide (CGRP). It consists of 52 amino acids in human and 50 amino acids in the rats [2, 3]. ADM can bind to the CGRP receptor in several types of tissues [6, 7], but specific ADM receptors that are insensitive to CGRP receptor antagonist have been identified . McLatchie et al.  demonstrated that the combination of calcitonin receptor-like receptor (CRLR) and receptor activity-modifying protein (RAMP) isoforms determines the ligand selectivity for CGRP and ADM. Coexpression of CRLR with RAMP1, RAMP2 and RAMP3 produces the CGRP, the ADM1 and ADM2 receptors respectively.
ADM is synthesized and secreted by various organs and tissues, including the heart, kidney, lung, adrenal gland and reproductive organs, such as the ovary [10–14], the uterus [10, 15], the oviduct , the testis [16–19], the prostate [20, 21], and the epididymis . Since its discovery as a potent vasodilator, there have been extensive studies on the pleiotropic effects of ADM [23–26]. Remarkable increases in plasma ADM concentrations were reported in both in human  and the rat  during pregnancy. ADM found in granulosa cells enhances progesterone production in human  and suppresses FSH-stimulated granulosa cell differentiation in the rat  by an autocrine action. The increases in ADM expression and binding sites in the rat uterus in late gestation  may be related to the inhibitory role of ADM in uterine contractility [15, 29]. The infusion of an ADM antagonist (hADM22-52) during early or late gestation in the rats caused fetoplacental growth restriction [30, 31]. The Adm-/- mice are non-viable [32–34]; and the haploinsufficient (Adm+/-) female mice were reported to have reduced pregnancy success , in support of a highly essential role for ADM in gestation especially in fetal growth and development. The expression of ADM and its receptors in the ovary and the oviduct of the cycling rats has been studied by our group and ADM was found to inhibit FSH-induced estradiol secretion from follicles and eCG-stimulated progesterone release in corpora lutea . We hypothesize that the distribution and levels of ADM and its receptors may change at different stages of pregnancy according to the roles of ADM. The expression of ADM and its receptors in the uterus, the oviduct and the corpus luteum in the rats of early, mid- or late pregnancy was therefore studied for possible physiological roles of ADM during gestation.
Mature Sprague-Dawley rats (12-13 week old) were obtained from the Laboratory Animal Unit, LKS Faculty of Medicine, the University of Hong Kong. Female rats showing three consecutive regular oestrous cycles were included in this study. The rats were housed at a constant temperature, humidity, under a 12-hour light-dark cycle (dark period 07:00 h to 19:00h) and rat chow and water were available ad libitum. Proestrus females were caged with proven fertile males overnight. The presence of vaginal sperm the following morning was taken evidence of pregnancy and this was day 1 of pregnancy. Rats of pre-implantation, early, mid- and late pregnancy were killed on days 3, 7, 12 and 17 of gestation. Pseudopregnant females obtained by mating with vasectomized male rats were also killed on day 7 of pseudopregnancy. Diestrus females were killed as nonpregnant controls. The uteri were dissected and implantation sites and inter-implantation sites were separated on days 7, 12 and 17 pregnancy. The foetuses and placentae of day 12 and 17 pregnant rats were collected before the dissection of the uteri. The ovaries were collected and the corpora lutea were isolated under a dissecting microscope using two 26G syringe needles. The oviducts were also collected and all the tissues were snap-frozen in liquid nitrogen and stored at -80°C for further analysis. Freshly collected intact uteri, ovaries and oviducts were fixed in neutral buffered formalin for immunohistochemical study. All procedures were approved by the Committee on the Use of Live Animals for Teaching and Research, the University of Hong Kong.
Genes expression of Adm, Crlr, Ramp1, Ramp2 and Ramp3
Total RNA of the uterus, corpus luteum, oviduct, foetus and placenta were extracted using TRIZOL reagent and subjected to real-time RT-PCR analysis. RNA samples (1 μg) were reverse transcribed into cDNA with the iScript reverse transcriptase according to the manufacturer's instructions (Bio-Rad Laboratories, Hercules, CA). The real-time RT-PCR technique has been previously described . Standard curves for each primer pair were prepared using serial dilution of the cDNA to determine PCR efficiency. The PCR efficiencies for Adm, Crlr, Ramp1, Ramp2, Ramp3 and Actb were all above 0.95 and similar. The relative gene expression levels normalized to Actb were analyzed using the ΔΔCT method, where CT was the cycle threshold. The reaction mixtures contained 25 μl iQ SYBR Green Supermix (Bio-Rad Laboratories, Hercules, CA), 500 nM of each primer, 1 μl template cDNA, and DNase-free water to a final volume of 50 μl. Cycle conditions were 95°C for 10 min, followed by 40 cycles of 95°C for 45 sec, 59°C for 30 sec, and 72°C for 45 sec. The reaction was completed with a dissociation step for melting point analysis from 50°C to 95°C (in increments of 0.5°C for 10 sec each. The primers were designed on the basis of the published sequences of Adm (caggacaagcagagcacgtc, forward; tctggcggtagcgtttgac, reverse); Crlr (ccaaacagacttgggagtcactagg, forward; gctgtcttctctttctcatgcgtgc, reverse); Ramp1 (cactcactgcaccaaactcgtg, forward; cagtcatgagcagtgtgaccgtaa, reverse); Ramp2 (aggtattacagcaacctgcggt, forward; acatcctctgggggatcggaga, reverse); Ramp3 (acctgtcggagttcatcgtg, forward; acttcatccggggggtcttc, reverse) and Actb (ggaaatcgtgcgtgacatta, forward; aggaaggaaggctggaagag, reverse). Melt curve analysis for each primer set revealed only one peak for each product. The size of the PCR products was confirmed by comparing the size of the product with a commercial ladder after agarose gel electrophoresis.
Immunohistochemistry was performed on 5 μm sections of paraffin-embedded tissues with a peroxidase-labeling kit (Vector Laboratories, Burlingame, CA). The antiserum against rat ADM (Phoenix Pharmaceuticals, Burlingame, CA) was used at a final dilution of 1:500. Staining was visualized using a DAB substrate kit for peroxidase (Vector Laboratories, Burlingame, CA). The antibody was omitted from control sections to check for nonspecific staining.
Extraction of ADM from the uterus, ovary, oviduct, foetus and placenta
Tissues including the uterus, corpus luteum, oviduct, foetus and placenta were homogenized in 2N ice-cold acetic acid and then boiled for 10 min. A 50 μl aliquot was taken for Bio-Rad protein assay (Bio-Rad Laboratories, Hercules, CA). The remaining homogenates were centrifuged at 18, 600 × g for 20 min at 4°C. The supernatants were lyophilized and stored at -20°C.
ADM Enzyme Immuno Assay (EIA)
The lyophilized tissue samples were reconstituted in 1X ADM EIA assay buffer. ADM peptide concentrations were measured in duplicates using an ADM (1-50) (rat) EIA kit (Phoenix Pharmaceuticals, Burlingame, CA). The minimum detectable concentration was 0.15 ng/ml and the range was 0-100 ng/ml. The intra-assay and inter-assay errors were less than 5% and 14% respectively.
The data are expressed as mean ± SEM. When there was only one variable, One-way ANOVA with the Fisher's Least Significance Difference post-hoc test was employed. When there were two variables, 2-way ANOVA was used. The significance level was set at P < 0.05.
Expression of Adm and its receptor components in the uterus, foetus, placenta, corpus luteum and oviduct during pregnancy
ADM peptide levels in the uterus, foetus, placenta, corpus luteum and oviduct during pregnancy
Immunohistochemical study of ADM in the female reproductive system
In the oviduct, intense ADM staining was localized in the mucosal layer of the oviduct, especially in the ciliated epithelium from nonpregnant and pregnant rats (Figure 7D). The muscularis and serosa layers of the oviduct showed little ADM staining.
There was no staining in the negative controls (see Additional file 1, Figure S1).
To the best of our knowledge this is the first time course study of ADM and its receptor component proteins in pregnancy in the female reproductive tract and corpus luteum. In our previous study in the rat, the oviduct expressed the highest level of ADM in the female reproductive tract during the oestrous cycle ; but ADM and its mRNA have not been characterized in the pregnant rats. ADM was most intense in the ciliated epithelium. CGRP is known to inhibit contractility in the human oviducts  and CGRP-binding sites are found on the vascular smooth muscle cells . Endothelin 2 has been shown to stimulate oviductal contraction in the rat  and ADM may inhibit this effect (Liao, Ho, Tang and O, unpulished data). Recently, we have also demonstrated that the presence of sperm in the oviduct stimulates ADM production, which in turn stimulates ciliary beating in the rat  and human  oviducts. During pregnancy, the increase in ADM peptide in the pre-implantation period may be related to the presence of sperm in the oviduct as well as its inhibitory action on oviductal contraction, which facilitate the ova/embryo transportation into the uterus. The decreases in ADM peptide and Adm mRNA levels in late pregnancy and in Crlr mRNA in mid- and late pregnancy may indicate that this inhibition is less important after placenta formation.
The most dramatic changes in ADM peptide and mRNA expression occurred in the uterus during pregnancy. Both the Adm mRNA and ADM were differentially distributed between implantation and inter-implantation sites. The lack of a difference in Adm mRNA levels and ADM peptide levels between the nonpregnant uterus and the pseudo-pregnant uterus suggests that such changes in the implantation sites must be due to the contact between the embryo and the uterus instead of alterations in hormone levels in the systemic circulation. In early gestation, ADM levels and mRNA levels of Crlr, Ramp1, and Ramp2 in the inter-implantation sites were higher than in implantation sites, in line with a role for ADM to increase blood supply  and to inhibit uterine contractility . Adm mRNA levels in the implantation sites of the uteri from mid- and late pregnant rats were much higher than the inter-implantation sites. The differences were much less marked in ADM peptide levels, suggesting a possible increase in release. An increase in Adm mRNA level in the uteri of pregnant rats has been previously reported . Plasma ADM levels are elevated in pregnant rats [28, 43] and pregnant women , presumably due to secretion by the uterus [14, 41] for the adaptation of the vascular system to pregnancy . The very high level of Adm mRNA and high levels of Crlr and Ramp1 mRNA at late pregnancy suggests an increasingly important role of ADM towards term.
The gene expression levels of Crlr and Ramp1 were higher at the implantation sites of late pregnancy than those in the uteri of nonpregnant rats, in line with a previous report of an increase in ADM binding sites in late pregnancy . This change may increase the number of CGRP receptors and augment the action of ADM, the expression of which was also increased. It is pertinent to note that ADM has been shown to inhibit uterine contraction via the CGRP receptor . The increase in Crlr and Ramp1 gene expression from early to late pregnancy is also in line with the increase in CGRP receptor binding from day 7 of gestation . CGRP is found in the nerves in the uterus  and inhibits uterine contraction  and causes vasorelaxation of the uterine artery .
Active angiogenesis is observed during early to mid-pregnancy to meet the need for an increase in blood supply . ADM have been proposed to exhibit its pro-angiogenic actions through CRLR/RAMP2 and CRLR/RAMP3 receptors  or CRLR/RAMP2 receptor . The high Crlr, Ramp2 and Ramp3 expression levels in the uterus in early and mid-pregnancy might contribute to the increased action of ADM in angiogenesis. Immunohistochemical study showed that ADM were located mainly in the endometrial stroma, similar to the finding of Cameron et al. [10, 52]. In our study, a trend for an increase in ADM immunoreactivity was observed from nonpregnant uterus to the pregnant uterus. The nonpregnant and 3-day pregnant uteri showed limited ADM staining in the epithelial cells lining the uterus while in early pregnancy, stronger staining was localized not only in the epithelium, but also in the blood vessels. The intense ADM immunostaining in the blood vessels suggests both an angiogenic role  and a vasodilatory role  in the endometrial blood vessels for increasing blood supply. ADM may have multiple roles in the uterus, regulating angiogenesis and blood flow in early pregnancy and maintaining uterine quiescence at mid- and late pregnancy. Studies involving the infusion of ADM receptor antagonist in early  and late  gestation have also demonstrated the importance of ADM in placentation and embryo development. The infusion of the ADM2 receptor antagonist in late pregnancy produced similar results .
Both the levels of ADM peptide and Adm mRNA in the placenta were lower in late pregnancy than mid-pregnancy. The mRNA levels of Ramp3 also showed a similar decline. To the best of our knowledge, this finding has not been described before in the rat placenta. In human, the concentrations of ADM mRNA in the placenta were found to be greater at term than in the first trimester . The significance of these changes remains an enigma. The mRNA levels of Adm, Crlr, Ramp1 and Ramp3 in the foetus were higher in late pregnancy than mid-pregnancy. This is related to the importance of ADM in embryogenesis as ADM is involved in embryonic invasion, proliferation, and differentiation, based on the developmental expression patterns of ADM in the rat and mouse embryos . The Adm gene expression in the placenta was higher while the peptide levels were lower than those in the foetus in mid- and late pregnancy, suggesting an increase in ADM release from the placenta. Human placenta has indeed been proposed to be the source of foetal circulating ADM as the ADM concentration in the umbilical vein was higher than in the artery .
The corpus luteum was studied instead of the entire ovary because it contains most of the ADM, as reported here and by Li et al. . The mRNA levels of Adm, Crlr and Ramp2 and Ramp3 in the corpus luteum all increased in late pregnancy compared with nonpregnancy, pre-implantation and early pregnancy and ADM peptide levels also increased at late pregnancy compared with early and mid-pregnancy. These increases may be related to the postulated roles of ADM in anti-luteolysis  and the production of progesterone . ADM appears to play a double role in corpus luteum progesterone production in that it is inhibitory in early and late pregnancy but stimulatory in mid-pregnancy (Li et al. unpublished data). The stimulatory effect of ADM on steroidogenesis has been reported in human granulosa-lutein cells .
In summary, there is a spatio-temporal pattern for the gene expression levels of Adm and its receptor components - Crlr, Ramp1, Ramp2 and Ramp3, the ADM peptide concentration and localization in the rat female reproductive system during gestation. In the oviduct, an increase in ADM peptide was found only in the preimplantation stage when the gametes/embryos were present in this part of the reproductive tract. During early pregnancy, the contact of embryo in the implantations sites upregulated ADM peptide and mRNA expression. The increase was further augmented in mid-pregnancy and similar increase was found in the placentae and the expression was comparatively low in the foetuses. A dramatic increase in ADM peptide and mRNA expression was also found in the corpus luteum during mid- and late pregnancy. All these changes suggest important roles for ADM in the maintenance of pregnancy as well as embryogenesis.
This study was substantially supported by a grant from the Research Grants Council (RGC) of the Hong Kong Special Administrative Region, China (HKU 7736/07M).
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