In women demise of the corpus luteum in the absence of pregnancy results in a rapid decline in peripheral progesterone that precipitates a cascade of molecular changes which induce myometrial contractions and vasoconstriction of the spiral arterioles of the endometrium. The net result of these changes is the generation of a hypoxic microenvironment in the upper, decidualised, functional layer of the endometrium which is typical of that associated with tissue necrosis and ischaemic injury [1]. Under normoxia, cellular oxygen sensors hydroxylate specific proline residues in the HIF-1α (hypoxia inducible factor-1 alpha) protein targeting it for rapid proteasome dependent degradation [2, 3]. Under hypoxic conditions, degradation of HIF-1α does not occur and the protein translocates to the nucleus where it forms heterodimeric binding complexes with HIF-β [4]. The HIF heterodimer binds to hypoxic response elements, acting as a transcription factor regulating expression of hypoxic response genes a number of which are expressed in the endometrium during menses [5–7].
HIF1α protein and its mRNA have been identified in the human endometrium, however the number of samples recovered during the menstrual phase was low with only n = 2 [5]. Previous studies using HIF expression as a surrogate for detection of hypoxia in the endometrium have yielded inconsistent results [5, 8]. As HIF is notoriously unstable it is possible that expression is lost during tissue collection and fixation or that the duration of hypoxia was too brief to stabilise enough HIF for immunohistochemical detection.
There is some disagreement in the literature as to whether hypoxia plays an essential role in regulation of tissue breakdown and initiation of repair during menses. Notably it is reported that the pattern of immunoexpression of HIF1α, HIF1β and HIF2α across the menstrual cycle is inconsistent with a role for hypoxia at menses [8]. Conversely in the same study, in vitro culture of endometrial stromal cells under hypoxic conditions resulted in an increase in intracellular HIF1α and VEGF [8] and together with data from Maybin et al. [9] would appear to support a role for hypoxia at menses.
These apparently contradictory results have prompted use of alternatives to immunohistochemistry including electron paramagnetic resonance (EPR) oximetry in combination with implanted particulate materials for in vivo measurement of oxygen tension. However, the use of these particulates does not generate images of the sample sites and successful EPR is highly dependent upon the microenvironment surrounding the particulate. A xenograft model of menstruation has utilised EPR in combination with lithium phtalocyanine (LiPc) crystals, which are sensitive to oxygen levels below 10 mmHg [10], this study reported no consistent evidence of hypoxia during menses. However, in this study the tissue was restricted to samples from the functional layer and therefore lacked the spiral arterioles of the basal layer that are thought to vasoconstrict at menstruation. An additional complication was that the model did not consider the role that the microenvironment of the flank engraftment site may play in xenograft establishment and HIF degradation during steroid induced ‘menstruation’ in the human tissue fragment.
The development of the Hypoxyprobe™ system facilitated direct visualisation of hypoxia in situ at oxygen concentrations of <1 %, irrespective of how long a cell has been under hypoxic conditions, but more importantly detection of the probe is resistant to fixation. The Hypoxyprobe™ system uses pimonidazole hydrochloride as its hypoxia marker, which forms protein adducts in hypoxic cells (pO2 < 10 mmHg) when administered in vivo. These protein adducts can be visualised by a specific monoclonal antibody. Detection of pimonidazole has been shown to be a reliable and direct measure of tissue hypoxia.
We hypothesised that hypoxia does occur during endometrial breakdown and that it is therefore likely to be a major player in promoting changes in gene expression that support rapid tissue repair at menses. Using the Hypoxyprobe™ in conjunction with a validated mouse model of rapid endometrial breakdown and repair revealed a spatial and temporal gradient of hypoxia in the endometrium which was associated with temporal changes in expression of angiogenic factors that are integral to restoration of a normal endometrial architecture.