Endometrial glands as a source of nutrients, growth factors and cytokines during the first trimester of human pregnancy: A morphological and immunohistochemical study
© Hempstock et al; licensee BioMed Central Ltd. 2004
Received: 14 June 2004
Accepted: 20 July 2004
Published: 20 July 2004
The maternal circulation to the human placenta is not fully established until 10–12 weeks of pregnancy. During the first trimester the intervillous space is filled by a clear fluid, in part derived from secretions from the endometrial glands via openings in the basal plate. The aim was to determine the activity of the glands throughout the first trimester, and to identify components of the secretions.
Samples of human decidua basalis from 5–14 weeks gestational age were examined by transmission electron microscopy and immunohistochemically. An archival collection of placenta-in-situ samples was also reviewed.
The thickness of the endometrium beneath the implantation site reduced from approximately 5 mm at 6 weeks to 1 mm at 14 weeks of gestation. The glandular epithelium also transformed from tall columnar cells, packed with secretory organelles, to a low cuboidal layer over this period. The lumens of the glands were always filled with precipitated secretions, and communications with the intervillous space could be traced until at least 10 weeks. The glandular epithelium reacted strongly for leukaemia inhibitory factor, vascular endothelial growth factor, epidermal growth factor, transforming growth factor beta, alpha tocopherol transfer protein, MUC-1 and glycodelin, and weakly for lactoferrin. As gestation advanced uterine natural killer cells became closely approximated to the basal surface of the epithelium. These cells were also immunopositive for epidermal growth factor.
Morphologically the endometrial glands are best developed and most active during early human pregnancy. The glands gradually regress over the first trimester, but still communicate with the intervillous space until at least 10 weeks. Hence, they could provide an important source of nutrients, growth factors and cytokines for the feto-placental unit. The endometrium may therefore play a greater role in regulating placental growth and differentiation post-implantation than previously appreciated.
The realisation that the maternal circulation to the human placenta is extremely limited prior to 10–12 weeks of pregnancy prompted us to investigate other potential sources of fetal nutrition during the first trimester [1–4]. During the evolution of ovoviviparity and viviparity secretions from the uterus became an increasingly important supplement to the yolk contained within the embryo's yolk sac . In chondrichthyan fishes they represent an important source of nutrients, even in those species that do not possess a placenta . Amongst eutherian mammals the uptake of secretions derived from the endometrial glands by the trophoblast continues to provide an important pathway for nutritional exchange in the earliest stages of pregnancy, before the placenta is established. These secretions contain a complex array of carbohydrates, proteins and lipids, and have been referred to variously as uterine milk or histiotroph . They are particularly significant in ruminants and equids where there is a relatively long interval between the arrival of the conceptus within the uterine cavity and the establishment of placentation. In some species, such as the pig and mouse, they represent a parallel pathway for the exchange of large proteins throughout most of pregnancy [7, 8].
More recently, it has been appreciated that the secretions may perform wider functions beyond the simple provision of nutrients. Some components, such as glycodelin, have potent immunosuppresive properties , while others, such as leukaemia inhibitory factor (LIF) and MUC-1, play key roles in regulating implantation [10, 11]. Histiotroph may therefore modulate materno-fetal interactions and regulate diverse aspects of placental development. Its importance during the preimplantation period has been powerfully demonstrated in the sheep, where suppression of endometrial gland development leads to failure of the conceptus to survive and develop . Equally, in the horse increased expression of epidermal growth factor (EGF) in the endometrial glands correlates closely both temporally and spatially with cell proliferation in the overlying fetal membranes .
In the human histiotrophic nutrition has always been considered to be of little importance for two principal reasons. Firstly, the invasive form of implantation displayed by the human blastocyst removes it from the uterine lumen, and hence it was believed the uterine secretions, by day 7–10 post-fertilisation. Secondly, the contemporaneous appearance of maternal erythrocytes within the lacunar spaces of the syncytiotrophoblastic mantle has been widely interpreted as evidence of early onset of the maternal circulation, and hence haemotrophic exchange [14, 15]. However, there is now a substantial body of evidence from a variety of techniques indicating that an effective maternal circulation is not established until the start of the second trimester [1, 3, 16, 17]. Indeed, the human placenta cannot be considered haemochorial prior to this time for the intervillous space is filled with a clear fluid only . Initially it was considered this fluid was derived as a plasma filtrate percolating through the trophoblastic plugs occluding the tips of the spiral arteries. However, we recently demonstrated that the uterine glands deliver secretions into the intervillous space until at least 10 weeks of gestation, suggesting that they may at least contribute to formation of the fluid . This raises the possibility that they may play greater roles during early pregnancy than previously anticipated, equivalent to those in other species.
The aim of this study was therefore to examine the secretory activity of the endometrial glands within the decidua basalis both morphologically and immunohistochemically over the first trimester in order to assess their potential contribution to fetal nutrition and placental development.
Samples of decidua basalis were obtained with informed written consent from patients undergoing surgical termination of normal pregnancies at University College Hospital, London. The study had been approved by the University College London Hospitals Committee on the Ethics of Human Research. Samples were obtained under ultrasound guidance, and were available from 30 cases ranging in gestational age from 5 weeks to 14 weeks (median age 9 weeks). Gestational age was estimated from the crown rump length of the fetus. Immediately after removal the tissues were fixed by immersion for 2 hours in either 4% paraformaldehyde in 0.1 M PIPES buffer for immunohistochemistry or 2% glutaraldehyde for electron microscopy, or frozen in OCT medium.
Primary antibodies used for immunohistochemistry.
Alpha tocopherol transfer protein
Dr D Kaempf-Rotzoll
Epidermal growth factor
Prof. M Seppälä
Human placental lactogen
Leukaemia inhibitory factor
Transforming growth factor β3
Vascular endothelial growth factor
Fluorescent dual-labelling immunohistochemistry
Paraformaldehyde-fixed samples of decidua basalis were embedded in paraffin wax, and sectioned at 5 μm. After rehydration sections were subjected to antigen retrieval by proteinase K (20 μg/ml for 30 min), permeabilised in TBS containing Triton X-100 (0.1%) and Tween 20 (0.1%) (TBS-TT) for 30–60 min and blocked in 5 % goat serum for 30 min at room temperature. A mixture of a rabbit polyclonal and a mouse monoclonal antibody diluted in TBS-TT was applied, and sections were incubated overnight at 4°C. Negative control sections were left at the blocking stage and were not covered with primary antibodies. After three 10-minute washes in TBS-TT, sections were incubated for 1 hr at room temperature with a mixture of fluorescent secondary antibodies, containing goat anti-rabbit Alexa 488 and goat anti-mouse Alexa 568 (both used 1/200; Molecular Probes) in TBS-TT. Sections were washed in TBS-TT as before and then twice in distilled water for 5 min and subsequently mounted in Vectashield mounting medium containing DAPI (Vector, UK).
Frozen sections were used for dual labelling with anti-cathepsin D (rabbit) and glycodelin (mouse). Samples were frozen in cryoembedding medium. Sections (10–12 μm) were cut on a Reichert cryomicrotome, air-dried, fixed briefly in cold methanol/acetone (at -20°C) and permeabilised in TBS-TT for 30–60 min. All subsequent immunolabelling steps were carried out as with the paraffin embedded sections. Images were captured using a Leica confocal microscope (LeicaTCS-NT, Leica Instruments GmbH, Germany).
Glutaraldehyde fixed tissues were secondary fixed in 1% osmium tetroxide for 1 hour, and embedded in Araldite epoxy resin. Semi-thin sections (1 μm) were stained with methylene blue, whereas ultra-thin sections (50 nm) were counterstained with uranyl acetate followed by lead citrate and viewed using a Philips CM100 microscope (Eindhoven, The Netherlands).
Archival histological material
The Boyd Collection housed within the Department of Anatomy, University of Cambridge, contains a number of placenta-in-situ specimens. Only those with no recorded history of pathology were reviewed, and twelve specimens met this criterion. The gestational age (from the last menstrual period) was estimated from the recorded crown-rump length , and ranged from 43 to 130 days. For each specimen the thickness of the endometrium was measured from the junction of the endometrium with the cytotrophoblastic shell perpendicularly to the border of the endometrium with the myometrium at a minimum of 50 randomly selected points spread over at least 5 slides using the VIDS system (Synoptics, Cambridge).
All analyses were performed using Statview (SAS Institute Inc., Cary, USA).
Mucin and Cytokine production
A similar pattern was observed for alpha tocopherol transfer protein (TTP) and transforming growth factor beta (TGFβ3), although many of the decidual cells also reacted positively as gestational age increased (Figure 9). In addition, some of the interstitial cells and those just beneath the epithelium reacted intensely for TGFβ3. These were presumed to be macrophages and uterine NK cells.
The pattern was different for epidermal growth factor (EGF), for although the glandular epithelium initially displayed strong reactivity, the intensity reduced considerably by 9–10 weeks. By contrast, in the older specimens the cells immediately beneath the epithelium reacted strongly. As these cells also reacted positively for CD56 it was assumed they were NK cells (Figures 7C,7D,7E,7F).
Immunoreactivity for lactoferrin was weak even in the earliest specimens, although occasional cells reacted strongly. In the older specimens only faint staining could be identified (Figure 9).
In all cases the negative controls showed no staining.
Fate of the secretions
It is clear from this study of placenta-in-situ specimens that the uterine glands are still well-developed and highly active at 6 weeks of pregnancy, and that although there is considerable individual variation they gradually regress, both in terms of their length and the height of their epithelium, as the first trimester advances. Some of this variation may reflect differences in the thickness of the endometrium across the placental bed, for it was generally thinnest in the centre and thicker towards the periphery. Sampling at different sites may therefore yield different measurements. Nonetheless, by the start of the second trimester the endometrium beneath the placenta is very thin, the glandular epithelium is cuboidal and secretory organelles are no longer predominant. Indeed, the accumulations of osmiophilic material within the cytoplasm are reminiscent of lipofuschin, a characteristic of involuting or aging cells. These observations are consistent with a gradual shift from essentially histiotrophic nutrition of the human conceptus during the early first trimester to haemotrophic nutrition towards the start of the second trimester [3, 20].
We previously reported that at 6 weeks gestational age the glandular epithelial cells closely resemble those during the luteal phase of the cycle, with large accumulations of glycogen within the apical portions of the cell [18, 21]. In the normal menstrual cycle these accumulations disperse around days 23–24, but their persistence indicates that the corpus luteum of pregnancy maintains the glands in a highly active state during early gestation. The composition of the secretions from the uterine glands has been extensively investigated during the various phases of the menstrual cycle [22, 23], but their contribution post-implantation has largely been ignored. The secretions are rich in carbohydrates, glycoproteins and, as demonstrated here, lipids. They therefore may provide an important source of nutrients for energy and elements for anabolic pathways within the feto-placental unit. The observation that glycodelin, a protein that is not expressed within placental tissues and so must be of maternal origin , enters the lysosomal digestive pathway within the syncytiotrophoblast supports this hypothesis. We have speculated that reliance on histiotroph during the period of organogenesis may protect the fetus from teratogenic damage by reactive oxygen species, for all mammalian embryos studied so far appear to rely heavily on anaerobic pathways during this period of development [25, 26]. Once organogenesis is complete the oxygen concentration within the feto-placental unit rises as placental attachment and development occurs or, as in the case of the human, the maternal circulation to the placenta is fully established.
Besides acting as a source of nutrients our results also demonstrate that the glands express a wide variety of growth factors and cytokines, and so may play an important role in regulating placental development as in other species. Receptors for EGF have been localised immunohistochemically to the cytotrophoblast cells in the earliest stages of pregnancy, and on the syncytiotrophoblast in later gestation [27, 28]. This switch parallels the dual actions of EGF reported, for in the earliest samples of 4–5 weeks EGF stimulated cytotrophoblast proliferation, whereas at 6–12 weeks it stimulated secretion of human chorionic gonadotropin (HCG) and placental lactogen . Similarly, receptors for LIF have been demonstrated on first trimester villous and extravillous trophoblast populations, and on villous endothelial cells . Addition of LIF to purified extravillous trophoblast cells had no effect on proliferation or integrin expression, but did inhibit forskolin-induced HCG production by BeWo cells in a dose-dependent fashion [30, 31]. Receptors for VEGF have also been identified on the villous and extravillous trophoblast populations, and on villous endothelial cells [32, 33], whilst TGFβ3 can modulate trophoblast differentiation between the proliferative and invasive phenotype . Histiotroph may therefore potentially play significant roles in regulating trophoblast proliferation and differentiation during early pregnancy, as well as modulating placental vascularization.
Another group of proteins expressed by the glandular epithelium is that of transport carriers. TTP is a cytosolic protein first identified in the liver, but which has recently also been reported in the syncytiotrophoblast of the human placenta [35, 36]. The high level of expression in the glandular epithelium suggests that histiotroph may be an important route for transfer of antioxidants during early pregnancy, increasing the defences of the feto-placental tissues against oxidative stress associated with onset of the maternal intraplacental circulation [3, 37]. Lactoferrin is glycoprotein (molecular weight 82,400) traditionally associated with the transport of iron in breast milk. It was first identified immunohistochemically in the endometrial glandular epithelium and in their secretions, and although immunoreactivity was variable between specimens it was generally strongest during the late secretory phase of the cycle . Here we identified significant staining only at the earliest gestational ages. The role of lactoferrin in the transport of iron is doubtful given the presence of transferrin receptors on the syncytiotrophoblast. Potentially, it may act as an antioxidant, for by forming stable complexes with free iron ions within the intervillous space it will reduce the possibility of generation of the highly toxic hydroxyl ion through the Fenton reaction [39, 40]. It also possesses anti-microbial properties and so may contribute to the immune defences of the endometrium and early placenta .
Endometrial secretions may also modulate maternal immunological responses to the placental tissues. Thus glycodelin, which is released into the intervillous space, is immunosuppressive and functions as a direct T-cell inhibitor [9, 42]. As gestation advances NK and stromal decidual cells migrate and come to lie closely approximated to the basal lamina of the glandular epithelium. The presence of NK cells within the glandular epithelium has been reported previously , and similar cells have been observed in an intraepithelial position in other species . Whether the subepithelial cells we observed play a role in immune surveillance or support the epithelium in some other way is not clear at present, but the fact that they are immunopositive for EGF raises the possibility of paracrine signalling.
Because insufficient decidualization could have an impact on implantation and placentation, evaluation of the endometrial morphology by ultrasound has generated a lot of clinical interest. An endometrial thickness of 8 mm or more is considered to be favourable for implantation in humans , although this remains controversial as other authors have not found an association between endometrial thickness and pregnancy achievement . One reason for this may be the fact that endometrial growth is not an homegeneous process, and that a single measurement of the endometrial thickness may not reflect the entire endometrial development. Within this context evaluation of the total endometrial volume with 3-D ultrasound could be a more accurate way of evaluating endometrial development . Adequate endometrial thickness seems to be directly linked to uterine vascularization, and women with a good endometrial thickness on ultrasound but a poor intra-endometrial blood flow tend to have a poor reproductive outcome . Uterine perfusion appears to regulate endometrial receptivity, and a high uterine resistance to blood flow is associated with recurrent miscarriages . The visualisation of the endometrial circulation with 3-D doppler ultrasound appears to be an efficient parameter in predicting implantation in IVF cycles .
Attempts to correlate functional activity of the glands with pregnancy outcome have also met with mixed success. Thus, whilst reduced concentrations of MUC-1, LIF and glycodelin in uterine flushings have been reported in women suffering recurrent miscarriages [51, 52], expression of these markers within the endometrium shows no significant association . Why the glands should regress while maternal progesterone concentrations remain high is not known, but it would seem reasonable to assume that the decline of histiotrophic nutrition and the onset of haemotrophic exchange are co-ordinated in some way. How this might be achieved in the human is unknown at present.
The authors are grateful to WellBeing for financial support, and to Prof. M Seppälä and Dr D Kaempf-Rotzoll for their gifts of antibodies. Ms O Spasic-Boskovic and Ms J Powell provided excellent technical assistance. The confocal and electron microscopy was performed in the Multi-Imaging Centre of the School of Biological Sciences, which was established with grants from The Wellcome Trust.
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