Biology and physiology of Calbindin-D9k in female reproductive tissues: Involvement of steroids and endocrine disruptors
Although Calbindin-D9k (CaBP-9k), a cytosolic calcium binding protein which has calcium binding sites, is expressed in various tissues, i.e., intestine, uterus, and placenta, potential roles of this gene and its protein are not clearly understood. Uterine CaBP-9k may be involved in controlling myometrial activity related with intracellular calcium level and is not under the control of vitamin D despite the presence of vitamin D receptors. But, it is under the control of the sex steroid hormones, estrogen (E2) and progesterone (P4), in female reproductive systems including the uterus and placenta. Thus, in this review, we summarize recent research literature in regards to the expression and regulation of CaBP-9k in mammals and introduce the research data of recent studies by us and others.
KeywordsEstrous Cycle Endocrine Disruptor Estrogenic Compound Estrogen Response Element Estrogenic Chemical
A 9-kilodalton cytosolic calcium-binding protein termed as Calbindin-D9k (CaBP-9k) belongs to a family of intracellular proteins which have high affinities for calcium, and has two calcium binding domains . The full-length cDNA encoding the human CaBP-9k has been cloned using reverse transcription/PCR, which includes coding region of 79 amino acids, 57 nucleotides 5'- and 159 nucleotides 3'-non-coding region, and a poly(A) tail (total 600 nucleotides in length) . Further, our study revealed that this gene spans about 5.5-kb and is localized on the X-chromosome, consists of three exons and carries four Alu repeats . In addition to its genomic structure, a sequence of 50 nucleotides downstream from the promoter showed an extensive homology to the estrogen response element (ERE) at the same location within the rat calbindin-D9k gene, suggesting that a two-nucleotide change within this region in human causes the gene to lack expression in human uterus and placenta .
It has been demonstrated that CaBP-9k is expressed in diverse mammalian tissues, i.e., intestine, uterus, kidney, and bone [4, 5, 6, 7]. The functional role of CaBP-9k is involved in intestinal calcium absorption and its gene is regulated at the transcriptional or post-transcriptional level by 1,25-dihydroxyvitamin D3 (1,25-(OH)2D3), a hormonal form of vitamin D [8, 9]. This hormonal form caused a parallel increase in CaBP-9k mRNA and intestinal absorption of calcium in rats . In addition, uterine CaBP-9k may be involved in controlling myometrial activity related with intracellular calcium level , but an exact role of CaBP-9k in the uterus is still under investigation by us and a few of other research groups. Recently, we demonstrated that uterine CaBP-9k is responsive to exogenous estrogen (E2) and can be a biomarker for environmental estrogenic chemicals, so called as "endocrine disruptors" in rat models [11, 12, 13, 14, 15]. Thus, in this review, we summarize recent research literature in regards to the expression and regulation of CaBP-9k in mammals and introduce updated research results by us and others.
Uterine expression of CaBP-9k
It has been demonstrated that CaBP-9k is mainly expressed in the endometrial stroma and myometrium of the uterus in non-pregnant rats [16, 17], whereas this gene is translocated into the epithelium of the uterus in pregnant rats . However, it has been shown that the CaBP-9k is only expressed in the luminal and glandular epithelium of the endometrium, not in the myometrium and in the stromal cells of the endometrium in non-pregnant cows . In contrast to the regulation of CaBP-9k in the intestine, CaBP-9k gene is not under the control of vitamin D in the uterus despite the presence of vitamin D receptors in this tissue. This gene appears to be under the control of the sex steroid hormones [17, 20, 21].
In contrast to the uterus of rats, the expression of CaBP-9k gene is not under strict E2 regulation in the uterus of mice. The uterus of mice has been demonstrated to express CaBP-9k and its level increases in this tissue during early pregnancy and implantation [28, 29]. CaBP-9k mRNA is expressed in the endometrial epithelia, both luminal and glandular, in the uterus at the time of implantation, and in the luminal, but not in the glandular, epithelia on early pregnancy (day 5 of pregnancy). P4 enhanced CaBP-9k mRNA expression in the uterus, whereas E2 did not in the oophorectomized adult mice . A higher expression of CaBP-9k mRNA was observed in the uterus of mice at diestrus and metestrus, whereas only basal level of its expression at proestrus and estrus, and E2 alone did not induce uterine CaBP-9k mRNA in this study . Taken together, these results suggest the complex hormonal regulation of CaBP-9k in the uterus of different species. To date, there was no evidence that CaBP-9k gene may be regulated by E2 in female reproductive tract of mice. In the recent study, we demonstrated that RU486, a P4 antagonist, induced a significant decrease in CaBP-9k mRNA expression, whereas tamoxifen and ICI 182,780, an E2 antagonists, had no effect on CaBP-9k mRNA expression, suggesting that P4, not E2, is a key regulator of CaBP-9k mRNA expression during late pregnancy and lactation in the uterus of mice .
The mechanism involved in the regulation of uterine CaBP-9k gene by steroids is relatively well understood in rats. In the uterus of rats, estrogen is known to up-regulate and progesterone down-regulate the expression of CaBP-9k gene during estrous cycle and early pregnancy [20, 22, 24, 25]. The expression level of CaBP-9k mRNA fluctuates during the estrous cycle, but shows very different expression pattern in the uterus of between rats and mice as abovementioned . The mechanism of distinct regulation of CaBP-9k gene between the rat and mouse is not clear at the moment. The effect of E2 on the regulation of CaBP-9k appears to be mediated through an imperfect estrogen-responsive-like element (ERE) identified in the intron A of mouse CaBP-9k gene [8, 24]. The regulation of this gene is known to be mediated by an E2 response element located at the first intron of rat CaBP-9k gene . Recently, cloning of intron A of the mouse CaBP-9k gene have revealed single-base difference in the ERE compared to that of the rat . This may partially explain the observed difference in the hormonal regulation of CaBP-9k gene in the uterus of between rats and mice. In addition, a distinct regulation of porcine CaBP-9k gene in the uterus is explained by no presence of a functional ERE within intron A region . However, we can not rule out the possibility of involvement of other unknown cell-, tissue-, and species-specific factors in the CaBP-9k gene expression. This idea is supported by the finding that E2 regulation of CaBP-9k gene in rats was only uterine-specific and this does not occur in the intestine . Although the putative ERE failed to bind to the estrogen receptor (ER) from the mouse uterus, we isolated mouse genomic clones of the CaBP-9k gene and analyzed their expression in the mouse uterus . In addition, we found a promoter region of CaBP-9k gene containing the putative progesterone response element (PRE) and its expression was stimulated by P4, suggesting that the mouse uterine CaBP-9k gene is expressed under the control of a PRE . In the recent study, we demonstrated that P4 and PR may be a dominant factor in the regulation of CaBP-9k and E2 and ERα can also influence the expression of CaBP-9k gene via an indirect pathway in the uterus of immature mice . Currently, endocrine disruptor-induced expression of CaBP-9k mRNA and protein was reversed or abolished by pretreatment with RU486 or ICI 182,780, suggesting that these synthetic chemicals may have both progestogenic and estrogenic properties by acting through PR or ER in the induction of uterine CaBP-9k mRNA and protein in the uterus of immature mice .
Uterine induction of CaBP-9k as a biomarker for endocrine disruption
Endocrine disruptors (EDs) are environmental chemicals that interfere with physiological systems, adversely affecting hormone balance (endocrine system) or disrupting normal function in the organs that hormones regulate or modulate, for example, female and male reproductive system . Representative example of suspected environmental estrogenic EDs includes the drugs which have been specifically designed to treat hormone imbalance in humans. These estrogenic compounds, including octylphenol (OP), nonylphenol (NP), bisphenol A (BPA), and methoxychlor (MXC), can also be transferred through the placenta to the fetus and through breast milk to infants [11, 13, 37]. Screening methods to detect endocrine disrupters have been evaluated by many groups, i.e. the receptor binding assay, reporter gene assay, and immature rat uterotrophic assay. The reporter gene assay has many benefits as a promising prescreening procedure, because this assay could be performed as a high throughput screening process to detect an endocrine disruptor from thousands of chemicals and no use of experimental animals is required . To screen estrogenic chemicals in the induction of endocrine disruption, genetically sensitive animal models, mice and rats, should be developed. Efforts to identify the mechanisms of endocrine disruption by estrogenic chemicals need to be supported for optimal test methods for thousands of potential chemicals in reproductive development and function . Thus, we have recently established a sensitive method to detect CaBP-9k mRNA and protein using immature rats, which can be used as a biomarker for endocrine disruptors, thus, we introduce our current results in regard to estrogenic effect of endocrine disruptors in the uterus of immature rats . Among the assays for the estrogenic activity of chemicals, an assay to detect an endogenous gene expression that measures estrogen-induced changes either in cultured cells or in selected tissues from exposed animals has been proposed and is widely being used. In our previous study, we demonstrated that phthalate esters exhibit a weak estrogenic activity in vitro assay at high concentrations. Although phthalates resulted in an increase in MCF-7 cell proliferation by estrogenic effect, they could not induce CaBP-9k expression in vivo system following oral treatments, assuming that these phthalates are easily metabolized to inactive forms in vivo system. These results suggest that a conflict may exist in estrogenic effect by various phthalates between in vitro and in vivo models related to the expression of CaBP-9k .
Placental expression of CaBP-9k
Transport of Ca2+ through placenta is responsible for developing fetus, and CaBP-9k appears to play an important role in the regulation of Ca2+ from the mother to the fetus during pregnancy. However, the role of CaBP-9k is unknown to date in placenta during pregnancy. A recent study demonstrated that CaBP-9k transcript is present in cytotrophoblast cells and syncytiotrophoblasts of human term placenta, with a lower expression in cytotrophoblast cells as compared to syncytiotrophoblasts . In addition, CaBP-9k protein was present in cytotrophoblast and syncytiotrophoblast placental tissue sections as well as in cultured cells, indicating that CaBP-9k is unequivocally expressed by trophoblast cells from human term placenta . The expression of CaBP-9k gene has been investigated in the placenta of other species [26, 46, 47, 48]. The high level of CaBP-9k has been localized to epithelial cells of the yolk sac and endodermal cells of the placenta . The expression of CaBP-9k mRNA was not detectable by Northern blot analysis, while this transcript was detected in porcine myometrium and placenta by RT-PCR . As previously described, CaBP-9k mRNA has been also localized in the trophoblasts in various species. It is hypothesized that CaBP-9k plays a role in calcium transfer and fetal growth by parallel gestational changes in placental CaBP-9k which reflects the fetal accumulation of calcium. An increased level of CaBP-9k gene in the caruncular epithelium during the last trimester is in response to the increasing need for calcium to supply the fetal skeleton with mineralization, suggesting that CaBP9k may play a role in transporting calcium across the placenta in cattle . In the placenta of mice, the distinct regulation of CaBP-9k has been demonstrated in the placenta compared to other tissues such as intestine and kidney, indicating that the expression of this gene is not dependent on Vitamin D receptor . Recently we demonstrated the expression of CaBP-9k for the first time in mouse placenta and extra-embryonic membrane separately, and CaBP-9k mRNA may be regulated by sex steroid hormones (E2 and P4) and their receptors through complex pathway in these tissues .
Although CaBP-9k is mainly expressed in female reproductive tissues, i.e., uterus and placenta of various species, the role of CaBP-9k remains unknown. It can be hypothesized that uterine CaBP-9k may be involved in controlling myometrial activity related with intracellular calcium level and placental CaBP-9k plays a role in calcium transfer from the mother to the fetus for fetal growth. It appears that CaBP-9k gene is not under the control of vitamin D in the uterus despite the presence of vitamin D receptors in this tissue; instead it is under the control of the sex steroid hormones. The hormonal mechanism controlling uterine CaBP-9k gene is relatively well understood in the rat. In the uterus of rats, estrogen is known to up-regulate and progesterone down-regulate the expression of CaBP-9k gene during estrous cycle and pregnancy. However, the recent studies demonstrated that CaBP-9k is mainly regulated by progesterone, not estrogen in the uterus of mice because of lack of responsiveness caused by a single-base difference in the ERE of mouse CaBP-9k gene compared to that of rats. Until now, a few studies demonstrated the expression and regulation of CaBP-9k gene in the placenta of various species. It appears that CaBP-9k mRNA may be regulated by sex steroid hormones (E2 and P4) and their receptors through complex pathway in these tissues. We assumed that ERα may be a key mediator in uterine CaBP-9k gene induction in immature rats. The elucidation of other factors that regulate CaBP-9k mRNA will further provide insight into the understanding of regulation of CaBP-9k in these tissues, and its roles in the control of reproductive functions.
The uterus is a highly estrogen-responsive tissue, which can be measured through changes in CaBP-9k expression. We demonstrated that the expression levels of CaBP-9k mRNA and protein are induced by estrogenic chemicals, so called "endocrine disruptors", in the uterus of immature rats. In addition, maternally injected estrogenic compounds resulted in an increase of CaBP-9k mRNA and/or protein in the fetal uterus during late pregnancy, suggesting that placenta may not be a reliable barrier against these estrogenic compounds for fetal health. It is of interest that maternally injected estrogenic compounds may be transferred to neonates through breast milk and thus affect uterine function, as shown by the induction of CaBP-9k gene expression in neonatal uterus. The expression of CaBP-9k mRNA and/or protein is an excellent biomarker to detect an estrogenic chemical in the uterus of immature rats which we developed and established. Availability of this gene using immature rats will provide an insight of risk assessment for estrogenic and progestogenic chemicals in our environment.
This work was supported by the research grant of the Chungbuk National University in 2005. The authors would like to thank Mr. Geun-Shik LEE (College of Veterinary Medicine, Chungbuk National University) for editing the figures.
- 5.Mathieu CL, Burnett SH, Mills SE, Overpeck JG, Bruns DE, Bruns ME: Gestational changes in calbindin-D9k in rat uterus, yolk sac, and placenta: implications for maternal-fetal calcium transport and uterine muscle function. Proc Natl Acad Sci U S A. 1989, 86: 3433-3437.PubMedCentralCrossRefPubMedGoogle Scholar
- 41.Hong EJ, Choi KC, Jeung EB: Maternal Exposure to Bisphenol A during Late Pregnancy Resulted in an Increase of Calbindin-D9k mRNA and Protein in Maternal and Postnatal Rat Uteri. J Reprod Dev. 2005, In press:Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.