Patent Application
20070254309
This application claims the benefit of Australian provisional application No. 2006902064 entitled “Methods for assessing embryo viability”, which was filed 20 Apr. 2006. The entire disclosure of this provisional application is incorporated herein by reference.
The present invention relates generally to methods of assessing embryo viability, in particular assessing the viability of embryos produced by assisted reproductive technologies such as in vitro fertilization.
Failure of survival of the embryo over the first weeks of its existence is considered to be a major cause of sub-fertility and infertility in mammals. This is particularly exemplified by embryos produced by assisted reproductive technologies (ART), including in vitro fertilization (IVF) and all related techniques. Not only is ART commonplace in human medicine, largely as a treatment for infertility, but it is also widely employed in agriculture to increase the rate of genetic gain in animals and to enhance fertility in high value animals such as beef cattle and horses. Embryos produced by ART are also the only source of human embryos used in the production of embryonic stem cell lines.
It has long been known that ART results in a characteristic phenotype of slow embryo development in vitro resulting in embryos with fewer cells and more cells undergoing death by apoptosis (see O'Neill, C., 1998, Biology of Reproduction 58, 1303-1309). Upon transfer of cultured embryos there is a characteristic reduction in the rate of formation of normal fetuses (Bowman, P., and A. McLaren, 1970, Journal of Embryology and Experimental Morphology 23, 693-704). This phenotype is particularly severe in human embryos produced by ART. For the decade 1993-2002, human ART in Australia resulted in 9.1 live births per 100 embryos transferred (Bryant, J., et al., 2004, AIHW Cat. No. PER 26. Sydney: Australian Institute of Health and Welfare National Perinatal Statistics Unit, Assisted Reproductive Technology Series No. 8). This inefficiency of ART makes the technology expensive, causing it to be prohibitive for many otherwise suitable agricultural purposes and a significant financial burden for human medicine. Furthermore, the low rates of embryo viability encourage the transfer of multiple embryos, creating a significant risk of multiple birth with consequent poor obstetric outcomes. It is generally recognized that these poor outcomes are a consequence of the adverse effects of embryo culture on the early embryo.
The ability to screen an embryo's developmental potential and to detect those embryos with the greatest viability after embryo culture would alleviate many of these problems associated with ART. Not only would this greatly contribute to improving the success, efficiency and utility of ART in medicine and agriculture, but may also lead to new therapeutic modalities.
Studies measuring aspects of embryo metabolism have been found to show a correlation with embryo viability, but have not found general use due to complexity and cost of assays and their generally low predictive power. A retrospective clinical study of a novel non-invasive method of embryo selection based on the depletion/appearance of amino acids in the culture medium showed that the turnover of Asn, Gly and Leu, was significantly correlated with a clinical pregnancy and live birth. These correlations were independent of known predictors, such as female age, basal levels of FSH, embryo cell number and embryo morphological grade (Brison, D.R. et al., Hum. Reprod. 19, 2319-2324 (Oct. 1, 2004)). In another study (Turner, K., et al., 1994, Human Reprod. 9, 2362-2366), pyruvate uptake by embryos was related to their capacity for implantation. An association was also found between embryo morphology and pyruvate consumption. Morphologically good embryos were more likely to implant if they demonstrated an intermediate pyruvate uptake. No relationship was found between the type of infertility and pyruvate consumption of individual embryos. It was suggested that the ability of an embryo to implant is multifactorial and that both morphology and pyruvate uptake may be factors. The technical complexity of these assays and their relatively poor predictive power has meant that little progress has been made with their use as a routine assay of embryo viability. Further, whilst a positive association between the release of the autocrine embryotrophin platelet activating factor (Paf) and the developmental potential of an embryo has been found, the utility of the Paf assay has been constrained by its difficulty and reliability of extraction from embryo culture media. This makes its quantification and assay difficult, unreliable and time-consuming (O'Neill, C., 2005, Human Reproduction Update 11, 215-28).
The preimplantation embryo produces survival factors that act in autocrine loops to drive the proliferation and survival of the early embryo. ART induces a number a stresses which activate stress pathways within the early embryo. This in turn leads to the production of a number of factors important in the survival of the embryo. For example, the important stress sensor, p53 is normally maintained at very low levels in the pre-implantation embryo. However it has been demonstrated that p53 expression is upregulated in embryos produced by ART and that p53 is a significant factor in the high rate of embryopathy following ART (PCT/AU2004/001121, published as WO 2005/019440, the disclosure of which is incorporated herein by reference).
The present invention is predicated on the finding that several protein markers may released by a cultured embryo into its culture media and that the release of these factors is correlated with the viability of the embryo.
Accordingly, in a first aspect there is provided a method for determining the viability of an embryo or an embryo precursor, the method comprising:
In another aspect, there is provided a method of ranking an embryo or embryo precursor on the basis of its viability, the method comprising:
In one embodiment, the method comprises the step of selecting the embryo with the greatest viability.
In some embodiments of these aspects, the marker is selected from the group consisting of p53, Cav1.2 and catalase.
In some embodiments of these aspects the embryo precursor is a fertilized egg, a zygote or another pre-embryonic entity. The embryo or embryo precursor may be produced by assisted reproductive technology, such as in vitro fertilization.
In some embodiments of these aspects the step (c) of comparing the measured level of the marker in the culture medium to at least one level of the marker which is indicative of the viability of the embryo comprises comparing the level of the marker in culture medium with the level of the marker from a control sample. The control sample may be a positive control comprising pooled culture media from embryos having high viability, or a negative control comprising pooled culture media from embryos having low viability.
In some embodiments of these aspects the step (c) of comparing the measured level of the marker in the culture medium to at least one level of the marker which is indicative of the viability of the embryo comprises comparing the level of the marker in the culture medium to the level of the marker in two or more control samples.
In another aspect there is provided a use of a kit for determining the viability of an embryo or embryo precursor, the kit comprising at least one agent for measuring the level of a marker in culture media. The marker may be p53, in which case the at least one agent may comprise an antibody to p53.
Also provided is a method of screening a candidate agent for the ability to modulate the viability of an embryo or embryo precursor, the method comprising contacting a first embryo or embryo precursor with the candidate agent, culturing the first embryo or embryo precursor in vitro in culture medium, culturing a second embryo or embryo precursor which has not been exposed to the candidate agent in vitro in culture medium, measuring the level of a marker which is indicative of the viability of the embryo in the culture medium of the first and the second embryo or embryo precursor, comparing the measured level of the marker in the culture medium of the first and the second embryo or embryo precursor and thereby determining whether the candidate agent modulates embryo viability.
In another aspect there is provided a method of screening a candidate agent for the ability to modulate the viability of an embryo or embryo precursor, the method comprising contacting an embryo or embryo precursor with the candidate agent, culturing the embryo or embryo precursor in vitro in culture medium, measuring the level of a marker which is indicative of the viability of the embryo in the culture medium, comparing the measured level of the marker in the culture medium with at least one level which is indicative of the viability of the embryo and thereby determining whether the candidate agent modulates embryo viability.
The marker in any of the above aspects may be p53.
In certain embodiments of these screening methods, the candidate agent is a culture medium.
In some embodiments of these screening methods, the modulation of embryo viability is an increase in embryo viability.
In any of the aspects described above, the embryo may be an embryo of a non-human primate, equine, bovine, ovine, caprine, leporine, avian, feline, canine or a murine species. In particular embodiments, the embryo is a human embryo. Definitions
In the context of this specification, the term “comprising” means “including principally, but not necessarily solely”. Furthermore, variations of the word “comprising”, such as “comprise” and “comprises”, have correspondingly varied meanings.
As used herein the term “marker” refers to one or more cellular constituents or products produced by the developing embryo and released into the medium in which the embryo is being maintained or cultured. In the context of the present specification a marker is a polypeptide or oligopeptide or larger fragment thereof. As used herein the term “fragment”) refers to polypeptide sequence comprising a constituent sequence of a full-length protein defined as a marker above. In terms of the polypeptide, the fragment possesses qualitative biological activity in common with the full length protein. A biologically active fragment of a marker protein may typically possess at least about 50% of the activity of the corresponding full length protein, more typically at least about 60% of such activity, more typically at least about 70% of such activity, more typically at least about 80% of such activity, more typically at least about 90% of such activity and more typically at least about 95% of such activity. As used herein the term “polypeptide” means a polymer which comprises as series of amino acids linked together by peptide bonds. A polypeptide as used herein may consist solely of amino acids, or may be a glycoprotein or a lipoprotein. It will be understood that in the context of this specification that reference to the detection or measuring of the level of a marker is not intended to exclude the detection or measuring of the levels of two or more markers.
As used herein the term “embryo or embryo precursor” refers to a zygote or post-zygotic derivatives of a fertilized egg. In a human, the embryonic stage is considered to begin approximately 2 weeks post fertilization. The term “embryo precursor” therefore refers to any entity in the pre-embryonic stage following fertilization of the egg. The term thus includes a fertilized egg and a zygote.
The term “expression” as used herein refers interchangeably to expression of a gene or gene product, including the encoded protein and to portions thereof. Expression of a gene product may be determined, for example, by Western blot or immunoassay using an antibody or antibodies that bind with the polypeptide. Accordingly, in the context of the present invention, expression may refer to the expression of a protein marker or a polypeptide fragment thereof.
In the context of this specification, the term “viability of an embryo” and “embryo viability” mean the likelihood of survival of an embryo. For the purposes of the present invention, embryo viability may be reflected in a number of indicators. For example increased embryo viability may result in any one or more of increased embryo implantation rates following in vitro fertilization, decreased pre- and post-implantation embryo lethality, increased clinical pregnancy rates or increased birth rates. An increase in the proportion of viable embryos may be exhibited in any one or more of an increase in the proportion of embryos developing into morphologically normal blastocysts, an increase in the number of cells per blastocyst and a decrease in the number of cells in the embryo undergoing apoptosis.
The term “detecting” a marker as used herein means the identification of the presence or absence of a marker. “Measuring” the level of a marker involves the quantification of amounts the marker. The quantification may involve assigning a numerical value of concentration, amount, or it may involve comparing the level of the marker with the level of a marker from a comparator sample, such as a control sample or the level provided by a standard curve. Accordingly “measuring” the level of a marker in an embryo culture medium may involve comparing the level of the marker in the medium to the level present in a pooled medium from embryos of known viability. Pooled embryos of known high viability may be readily generated by obtaining, for example, blastocysts collected fresh from the reproductive tract. Pooled embryos of low viability may be readily generated by, for example producing blastocysts via IVF techniques described herein.
The present invention will now be described by way of example with reference to the accompanying figures.
Abbreviations
The expression of p53 has been demonstrated to be upregulated in embryos produced by assisted reproductive technologies (ART) such as in vitro fertilization (IVF) and that this upregulation correlates with poor embryo viability following ART (PCT/AU2004/001121, published as WO 2005/019440, the disclosure of which is incorporated herein by reference). Further, short term inhibition of p53 during the culture of embryos in vitro can increase the viability of embryos. For example the proportion of embryos developing into morphologically normal blastocysts can be increased, the number of cells per blastocyst increased and the number of cells in the embryo undergoing apoptosis decreased.
p53 is a transcription factor whose actions are normally located within the nucleus of cells. It is not generally considered a secretion product of cells. It has now been found, however, that p53 produced by embryos, in particular those generated by ART, is released into the in vitro culture medium and that this p53 release is inversely correlated with the viability of the embryo.
The detection of p53 in fluids, for example in sputum and in pancreatic juice and plasma of patients with pancreatic carcinomas has been reported. However, the presence of p53 and the p53 gene in these cases is due to the presence of exfoliated cells (see Gao et al., 2005). p53 has not previously been reported as being released by cells, nor have there been any reports of using protein release by cells as a diagnostic or predictive indicator of embryo viability or developmental potential.
In the present study two further normally intracellular survival/stress related proteins, Cav1.2 (a voltage-dependent calcium ion channel) and catalase, have also been detected in embryo culture media.
Accordingly, in one aspect there is provided a method for determining the viability of an embryo, the method comprising:
wherein the level of the at least one marker detected in the culture medium is indicative of the developmental potential or viability of the embryo.
The method for determining the viability of an embryo is of particular benefit in assessing embryo viability and developmental potential during ART, and in particular IVF. Other suitable ART techniques to which the method described herein is applicable include, but are not limited to, gamete intrafallopian transfer (GIFT), zygote intrafallopian transfer (ZIFT), blastocyst transfer (BT) and intracytoplasmic sperm injection (ICSI). Thus an application of the method is in the selection of the most suitable embryos for transfer during ART. However, those of skill in the art will appreciate that the advantages offered by the method are not limited to ART-generated embryos. Rather the methods for determining the viability of an embryo provided herein are equally applicable to assessing viability of any embryos, whether they are produced in vitro via ART or in the reproductive tract of the animal. The methods provided herein are therefore also applicable to assessing viability of embryos in otherwise unassisted pregnancies and thus the likelihood of the embryo developing to full term.
The methods and compositions provided herein are of use not only for human reproduction, but for a variety of species. For example the methods and compositions provided herein can be used to assess embryo viability in animal husbandry, for species of agricultural value, and in species bred for conservation purposes. In particular the present invention finds application in vertebrates, and more particularly in mammals. For example, while studies have identified that the expression of intracellular p53 is elevated in human embryos with retarded development or abnormalities, the present study has identified that the elevated intracellular levels of p53 are expressed in murine embryos having a similarly reduced viability.
Further, the methods and compositions provided herein also find applications in circumstances in which it is beneficial to determine embryo viability, for example in the production of embryonic stem cells, the production of cloned embryos and all related techniques.
As disclosed herein, in models where the levels of p53 expression is experimentally manipulated, the subsequent development of embryos to viable fetuses after embryo transfer was inversely related to their expression of p53 and the release of p53 into the culture medium; those conditions resulting in higher levels of p53 expression and release resulted in fewer embryos displaying normal development through to blastocyst stage. As demonstrated in WO 2005/019440, temporary inhibition of p53 in the developing embryo leads to a significant increase in the proportion of embryos developing normally to blastocyst stage (as well as an increase in the number of cells per blastocyst and a decrease in the number of cells in the embryo undergoing apoptosis). Therefore, it will be readily appreciated by those skilled in the art that the methods provided herein in combination with the methods and compositions for improving embryo viability as disclosed in WO 2005/019440 may provide powerful and valuable avenues for the screening and treatment of embryos in circumstances in which it is beneficial to improve embryo viability, for example in improving the success rates of ART, in producing embryonic stem cells and cloned embryos and in all related techniques.
The employment of methods provided herein may have further potential applications including in the quality control of embryo culture procedures and quality assurance of the manufacturing and procedural aspects of ART. The method provided herein may provide tools for the design and creation of a rational and effective means for improved embryo culture media design, laboratory equipment and procedures, risk assessment and quality assurance/ quality control procedures throughout the ART process. For instance, using the methods described herein to determine embryo viability animal embryos may be used to screen materials such as culture media or culture additives to determine whether they support or retard embryo viability in vitro. Such screening methods may be used, for example, in the development of new media for ART techniques, or in the batch screening of media for quality control purposes. Similarly, the methods described herein for identifying embryo viability following embryo culture may be used to develop new techniques and methods for embryo culture, or to monitor ongoing culture techniques for compliance to standards.
At present, quality control of routine ART laboratory procedures and media production is most commonly performed by the use of a mouse embryo toxicity test. In this assay a large number of embryos (˜100) are cultured from the zygote stage through to the blastocyst stage for each test parameter. Toxicity reduces the proportion of embryos that develop to the blastocyst stage. This assay successfully detects gross toxicity within culture systems, but has limited utility for detailed quality assurance, quality control or research and development due to the poor sensitivity and specificity of the assay. It is possible to improve the predictive power by performing embryo transfer procedures of these sentinel embryos to foster mothers, however this is prohibitively expensive, requires a further large number of animals as foster mothers, and requires a further 2-3 weeks before a result is available. The methods provided herein provide a more straightforward and rational alternative for quality control while avoiding or ameliorating the inherent disadvantages and problems associated with the mouse embryo toxicity test.
Included within the scope of the methods described herein is the detection and/or measurement of a one or more cellular markers released by the embryo or embryo precursor. Such a marker will be a polypeptide or oligopeptide fragment thereof, and may be a glycoprotein or a lipoprotein or oligopeptide fragment thereof, which is/are normally associated with cell or embryo survival and/or stress responses. By way of example only, markers may include p53 , Cav1.2 or catalase.
Accordingly, the detection of any one or more of these markers in culture medium from cultured embryos is contemplated in a method for determining the viability of an embryo.
As exemplified herein, protein markers such as p53, Cav1.2 and catalase in the culture medium may be detected and quantified using the method of Western blotting. Polyclonal antibodies to human and other species p53, for example, suitable for use in Western blots are available commercially, for example from Abcam (p53 antibody ab2433). However those skilled in the art will appreciate that the invention is not limited to the use of such a method. Any method, direct or indirect, that is able to detect protein or polypeptide presence and/or measure protein expression or concentration will be useful in determining the level of a protein or polypeptide and is contemplated as forming part of the present invention. For example, it will be apparent that ELISA kits for the detection of p53 are also commercially available (for example the p53 ELISA Kit, PathScan® from Cell Signaling Technology) and that these may be used in the quantification of p53 levels in culture medium either directly or following concentration of the p53 component in the culture medium.
Methods of the present invention may make use of one or more antibodies for the detection of protein and polypeptide markers and the determination of marker levels. The antibodies may be polyclonal or monoclonal and may be raised by the use of the protein marker or an antigenic fragment or portion thereof as an antigen. Antibody binding may be detected by virtue of a detectable label on the primary antibody. Alternatively, the primary antibody may be detected by virtue of its binding with a secondary antibody or reagent that is appropriately labeled to enable detection. A variety of methods are known in the art for detecting binding in an immunoassay and are within the scope of the present invention. For example determinations of protein and polypeptide marker levels can be accomplished by any one of a number of techniques known in the art including, for example enzyme-linked immunosorbent assays (ELISA); sandwich immunoassays, immunoradiometric assays (IRMA), radioimmunoassays (RIA), immunoelectrophoresis assays, in situ immunoassays, immunodiffusion assays, immunofluorescence assays, chromatographic assays, mass spectroscopy such as surface-enhanced laser desorption-ionisation time-of-flight mass spectrometry (SELDI-TOF MS), ligand-binding assays, and the like. Detection methods may be in the solid phase, such as chip-based assays for cost-effective and efficient testing of multiple samples. Where the level of the marker present in the culture medium is low, it will be understood that methods for the concentration of proteins or peptides in a sample, such as size exclusion ultracentrifugation concentration techniques, may be used to increase the level of the marker in order to increase the sensitivity of detection.
As contemplated herein, methods of the invention may include the step of comparing the level of the one or more markers in embryo culture medium with the level of the same one or more markers from a control sample. Typically the control sample may be: (1) media that is identical to the test media but not exposed to embryos; (2) a positive control media, that is, pooled media standards from embryos shown to have high developmental potential; (3) a negative control media, that is, pooled media standards from embryos shown to have poor developmental potential. These controls would be developed specifically for each species and indication for which the assay is used. When ranking embryos by viability, it is contemplated that embryos which release the least p53 into the culture medium, for example, are the most viable, and conversely, embryos which release the most p53 into the culture medium are the least viable.
Also provided herein are methods for the screening or identification of candidate agents useful for modulating embryo viability, the processes comprising contacting an embryo or embryo precursor with a candidate agent, culturing the embryo in vitro and determining whether the level of one or more markers in the culture medium is increased or decreased in the presence of the agent and thereby determining whether the agent is capable of modulating, i.e., increasing or decreasing embryo viability. Based on the observations described herein, should the presence of the candidate agent result in a reduction in the level of a marker such as p53 in the culture medium, the agent may be considered as an agent suitable for use in increasing embryo viability. The determination of whether the candidate agent increases or decreases the level of one or more markers may be made by comparing the level of the marker produced by an embryo exposed to the agent with the level of the marker produced by an embryo not exposed to the agent, or by reference to a standard curve which correlates embryo viability with the level of the marker.
Typically the candidate agents are compounds that are not previously known to inhibit the expression or activity of the one or more markers detected in the culture medium.
The present invention also relates to kits for the determination of the level of a marker indicative of the developmental potential or viability of the embryo in culture medium wherein the kits facilitate the employment of methods of the invention.
The present invention will now be further described in greater detail by reference to the following specific examples, which should not be construed as in any way limiting the scope of the invention.
General Methods
Mice and IVF: The strain of mice used in experiments was C57BL/6J. All animals were housed and bred in the Gore Hill Research Laboratory, St Leonards, NSW, Australia. All animals were under 12 h light: 12 h dark cycle and had access to food and water ad libitum. Four to eight week old females were superovulated by i.p. injection of 10 IU pregnant mare serum gonadotrophin (Folligon, Intervet International, Boxmeer, The Netherlands) followed 48 h later by 10 IU human chorionic gonadotrophin (hCG, Chorulon, Intervet). Females were paired with males of proven fertility. Day 1 of pregnancy was confirmed by the presence of a copulation plug the following morning.
Embryo collection and culture: Mice were killed by cervical dislocation. Cumulus masses or embryos were flushed from the reproductive tract with HEPES-buffered modified human tubal fluid medium (HEPES-modHTF—101.6 mM NaCl, 4.6 mM KCl, 0.2 mM MgSO4, 0.4 mM KH2PO4, 21.4 mM Na lactate, 1 mM glutamine, 2 mM CaCI2, 4 mM NaHCO3,0.33 mM Na pyruvate, 2.78 mM glucose and 21 mM HEPES buffer pH 7.35; 285 mOsm/l). All components of the media were tissue culture grade (Sigma Chemical Company, St Louis, Mo.) and contained 3 mg BSA /ml unless otherwise stated (CSL Ltd., Melbourne, Vic., Australia).
Zygotes were collected 20-21 h after hCG and freed from their cumulus cells by brief exposure to 300 IU hyaluronidase (Sigma) in HEPES-HTF. Embryos were thoroughly washed in three changes of Hepes-modHTF, recovered in minimal volume and assigned to various treatments as required in mod-HTF (same as Hepes-mod-HTF except that Hepes buffer was replaced with NaHCO3). Embryos were cultured in 10 μl volumes in 60-well HLA plates (LUX 5260, Nunc, Naperville, Ill.) overlaid by approximately 2 mm of heavy paraffin oil (Sigma). Plates were allowed to equilibrate in the culture incubator for at least 4 h before addition of the embryos. Embryos were cultured individually for 96 h at 370C in 5% C02. Fresh 2-cell embryos were collected on 40-42 h after hCG.
Immunolocalisation of p53 in mouse and human embryos
The expression pattern of p53 protein in pre-implantation mouse embryos was investigated using immunofluorescence.
Embryos were washed 3-times (washing media: PBS with 0.1% BSA, 0.1% Tween-20) and fixed with fresh 2% paraformaldehyde (Sigma) in PBS PH 7.4 for 1 h at room temperature. Embryos were permeabilised for 30 min at room temperature in PBS with 2% BSA, 0.2% Tween-20 and 0.2% Triton X-100 and blocked in 2% BSA and 30% blocking serum for 1-3 h. P53 antigen was stained overnight at 4° C. with 2 μg anti-p53 sheep polyclonal antibody/ml (Oncogene Research Products (PC35) or rabbit polyclonal anti-Bax (Santa-Cruz, N-20) in PBS with 2% BSA and then 5 μg rabbit anti-sheep FITC-conjugated antibody/ml for 1 h at room temperature (green channel). Controls were 2 μg non-immune IgG/ml instead of primary antibody. Immunofluorescence images were observed using a BioRad Radiance confocal microscope (Australian Key Centre for Microscopy and Microanalysis, University of Sydney) using a Nikon Plan Apo 60X/1.40 oil immersion objective. Images were captured using LaserSharp 2000 Version 4.0 (build 365) software. Microscope and laser settings were adjusted such that no fluorescence was observed with non-immune control. All test specimens were observed with these settings and settings the same. Quantitative analysis of staining was performed using NIH Image software. For imaging the whole embryo 1 μM sections were performed using the z-sectioning facility of the microscope.
The expression of immunodetectable p53 protein was low in preimplantation mouse embryos collected fresh from the reproductive tract (fresh embryos) (
A total of 8 human embryos from two couples were examined. Embryos were created by standard IVF as previously described in detail in Henman M, et al. 2005, Fertil Steril, 84:1620-7). Embryos were those excess to use by the treated couples and were donated with informed consent under NHMRC license 309702B.
Gametes were fertilized in Sydney IVF Fertilization media, and then cultured in Sydney IVF Cleavage media (48 h) followed by cultured in Sydney IVF Blastocyst media (all media from Cook). Following culture for this period embryos were frozen using a Sydney IVF Blastocyst Freezing Kit (Cook). Following culture individual embryo were placed in straws (IMV Technologies, France) and loaded into a rate-controlled freezer (Kryo 10 series II; Planar, Middelsex, England). Straws were cooled to −7° C. at 2°/min, then −7° C. to −30° C. at 0.3°/min, and from −30° C. to −150° C. at 35°/min, then plunged directly into liquid nitrogen at −196° C.
Blastocysts were thawed by removing the straw from the liquid nitrogen and exposing the straw to room temperature for 30 s, followed by 30 s in a 30° C. water bath. The straw was cut open onto a small dry petri dish and the contents moved promptly into the first of a four-stage thawing process (Sydney IVF Blastocyst Thawing Kit; Cook). Embryos were immediately fixed in formaldehyde and subjected to immuno-labelling for P53 as is described for mouse embryos.
Immunofluorescence procedures were the same for both human and mouse embryos. Embryos were washed 3 times in phosphate buffered saline (PBS) with 0.1% (w/v) bovine serum albumin, 0.1% (v/v) Tween-20 and 0.2% (w/v) sodium azide (washing buffer) and then fixed with freshly prepared 2% paraformaldehyde (w/v) (Sigma) in PBS (pH 7.4) for 30 min and then permeabilized with 2% paraformaldehyde with 0.3% Tween-20 (Sigma) at room temperature for a 30 min. Embryos were washed 3 times in washing solution and then were blocked in PBS containing 2% (w/v) BSA, and 30% (v/v) goat serum for 3 h. They were stained overnight at 40C with primary antibodies [1:500 anti-p53 (Ab-7) polyclonal antibody (Cat No: PC35, Oncogene Research Products) or an equivalent concentration of isotype control immunoglobulin (negative control). Primary antibodies were detected by incubation of embryos with secondary antibody coupled to FITC in PBS, 2% BSA for 1 h at room temperature. Optical sectioning was performed with a Bio-Rad Radiance Confocal microscope, using a Nikon Plan Apo 60X/1.4 oil emersion objective. Images were captured using Lasersharp 2000, Version 4.0 (BioRad). Microscope and laser settings were adjusted such that no fluorescence was observed with non-immune controls. All the test specimens were observed with these same settings.
Staining of the 8 human embryos for immuno-detectable p53 showed considerable within and between embryo heterogeneity of p53 expression. Four embryos with the morphology of normal blastocysts displayed generally low levels of p53 staining, but in some embryos showed some cells with clear p53 expression. One embryo showing retarded development and abnormal morphology displayed uniformly high levels of p53 expression in cells in an equatorial section. In a blastocyst that had a partially collapsed blastocoel, there were a large number of cells that showed p53 staining. Much of this staining appeared to be associated with the nuclear region of cells.
Expression of p53 was also identified in the zona pellucida and peri-viteline space, which is consistent with the observation in the mouse that under conditions of high p53 expression some of the p53 is released by the embryo.
This study shows that some embryos produced by ART manifest a high rate of p53 protein expression. The highest levels of p53 expression occurred in embryos with poor morphology.
p53 expression in mouse embryos
Western blot analysis was used to compare the expression of p53 protein in mouse embryos fertilized and grown in the reproductive tract without further culture and in IVF mouse embryos.
Two males 10-20 wk of age and of proven fertility were used for each IVF procedure. Following cervical dislocation, the epididymides were removed and placed into 1 mL of pre-equilibrated HTF in a petri dish. The epididymides were punctured with a sterile needle and the sperm gently squeezed out into medium. The dish was placed into an incubator at 37° C. with 5% CO2 in air for 40 min to allow sperm to disperse. Cumulus masses containing oocytes were then collected from female mice 15-17 h after the hCG injection and extensively washed in Hepes-HTF. Groups of approximately 30 oocytes with their associated cumulus masses were placed into 5 mL plastic tubes (Falcon; Becton Dickinson Labware, Lincoln Park, N.J.) in 1 mL of HTF. After dispersal of the sperm, they were thoroughly mixed and the concentration was assessed using a hemocytometer. Motile sperm (0.5×106) were added to each tube containing oocytes.
The fertilization rate was assessed at 5-6 h after insemination by visualization of pronuclei. All fertilized oocytes were extensively washed in Hepes-HTF to remove sperm and cumulus cells and then pooled. Embryos of all types were recovered in a minimal volume and assigned to various treatments as required.
Cells of the T47D breast cell line (Cat # HTB-133, American Type Culture Collection, Manassas, Va. USA) was used as a positive control for the detection of p53.
Embryos were collected and washed 3 times in cold PBS and transferred in a maximum volume of 1.5 μl PBS. Embryo culture media aliquots had embryos and all cells removed and then subjected to freeze drying. The lyophilized proteins were redissolved in 1.5 μl of water. Embryo or reconstituted culture media was mixed with 1.5 μl of 2X extraction buffer (2X PBS, 2% Triton X-100, 24 mM deoxycholic acid, 0.2% sodium dodecyl sulfate, 20 mM NaF, 20 mM Na4P2O7, 2 mM PMSF, 3.08 μM Aprotinin, 42 μM Leupeptin and 2.91 μM Pepstatin A-all from Sigma). The embryos were lysed by three cycles of freezing in liquid nitrogen and thawing (with vortexing).
Protein samples were diluted with 1 μl of 5X Laemmli buffer (50 mM Tris-HCl, 5 mM EDTA pH 8.0, 12.5% Sodium dodecyl sulfate, 0.05% bromophenol blue and 25% beta-Mercaptoethanol), incubated 10 min at 60oC and ran on 20% homogenous SDS polyacrylamide gels (Pharmacia) using PhastSystem apparatus (PhastSystem-separation and control unit, Pharmacia, Sweden).
Proteins were blotted into PVDF membranes (Hybond-P, Amersham Pharmacia) in a semi-dry blotting apparatus overnight using transfer buffer (12 mM Tris PH 7.0, 96 mM Glycine and 20% methanol). Nonspecific binding was blocked by 5% skim milk in PBS supplemented with 0.05% Tween-20 (PBST) at room temperature for 1 h. Membranes were probed with 1:500 diluted anti P53 antibody overnight at 4° C. in 2.5% skim milk, and detected with 1:500 diluted horse radish peroxidase (Jackson ImmunoResearch Laboratories, West Grove, Pa., USA) conjugated mouse antibody. Membranes were developed with Pico SuperSignal Chemiluminescent Substrate (Pierce, Rockford, Ill., USA) for 5 min at room temperature.
The results of these experiments are illustrated in
Detection of p53 in embryo culture media
Western blot analysis was used to determine the concentration of p53 protein within culture media resulting from the culture of mouse blastocysts produced by IVF, fertilised in situ and then cultured to blastocyst stage in vitro (ISF), or blastocysts collected fresh from the reproductive tract (fresh) and placed in media for 6 hours.
Embryos were collected from mice housed and bred in the Gore Hill Research Laboratories, St. Leonards, NSW, Australia, under a 12 hour light: 12 hour dark cycle and had access to food and water ad libitum. Four to eight-wk-old females were superovulated by intraperitoneal injection of 10 IU of eCG (Folligon; Intervet International, Boxmeer, the Netherlands) followed 48 h later by 10 IU of hCG (Chorulon; Intervet International).
For in situ fertilization (ISF) techniques embryos fertilization was by natural mating. Females were paired with males of proven fertility. Pregnancy was confirmed by the presence of a copulation plug the following morning (Day 0.5). ISF zygotes were flushed from the reproductive tract with Hepes-buffered modified human tubal fluid medium (Hepes-HTF) and were cultured in modified HTF medium (mod-HTF).
IVF was performed by collecting sperm from two males, 10-20 wk of age, and of proven fertility. Following cervical dislocation, the epididymides were removed and placed into 1 mL of pre-equilibrated HTF in a petri dish. The epididymides were punctured with a sterile needle and the sperm gently squeezed out into medium. The dish was placed into an incubator at 37C with 5% CO2 in air for 40 min to allow sperm to disperse. Cumulus masses containing oocytes were then collected 15-17 h after the hCG injection and extensively washed in Hepes-HTF. Groups of approximately 30 oocytes with their associated cumulus masses were placed into 5-ml plastic tubes (Falcon; Becton Dickinson Labware, Lincoln Park, N.J.) in 1 mL of HTF. After dispersal of the sperm, they were thoroughly mixed and the concentration was assessed using a hemocytometer. Motile sperm (0.5×106) were added to each tube containing oocytes. The fertilization rate was assessed at 5-6 h after insemination by visualization of pronuclei. All fertilized oocytes were extensively washed in Hepes-HTF to remove sperm and cumulus cells and then pooled.
All components of the media were tissue culture grade (Sigma Chemical Company, St. Louis, Mo.) and contained 3 mg/ml of BSA unless otherwise stated (CSL Ltd., Melbourne, Victoria, Australia). Zygotes were collected 20-21 h after hCG injection and were freed from their cumulus cells by brief exposure to 300 IU of hyaluronidase (Sigma Chemical Company) in Hepes-HTF. Embryos were recovered in minimal volume and were assigned to various treatments as required in mod-HTF.
Embryos were cultured in 10 μl volumes in 60-well human leukocyte antigen plates (LUX 5260; Nunc Inc., Naperville, Ill.) overlaid by approximately 2 mm of heavy paraffin oil (Sigma Chemical Company). Embryos were cultured in groups of 10. Culture was at 37° C. in 5% CO2 for the periods indicated in individual experiments.
Embryos were prepared by IVF or collected at the zygote stage (ISF) (Day 0.5) and were cultured in vitro for 90 h (cultured) or were collected directly from the uterus at the blastocyst stage (Day 3.5).
Media conditioned by 3,000 T47D cancer cells were used as a control.
As shown in
Thus, this experiment demonstrates that p53 is released by cultured embryos into the culture medium, and that in IVF embryos which are characterized by poor viability the amount of p53 which is released is elevated compared to embryos which are characterized by good viability.
Correlation of p53 concentration in culture media with embryo developmental potential
As illustrated in
In some experiments modHTF was supplemented with Paf (Sigma). An equal mixture of 1-o-octadecyl/hexadecyl-2-acetyl-sn-glycero-3-phosphocholine (Paf) was prepared as a lmg/ml stock solution in chloroform. Aliquots were removed to a siliconized glass test tube, reduced to dryness under a steam of N2 and dissolved in perfusion medium to the desired concentration. Culture was performed in a final concentration of 0.1 μM Paf.
Culture was performed normally under an atmosphere containing 20% oxygen except where indicated as low O2, where a mix of 5% O2, 5% CO2 in N2 was applied.
p53 was detected by Western blot as described above and densitometry was performed using Scion Image software (Scion Corporation, Frederick, Md., USA).
As illustrated in
The level of p53 release into culture media as illustrated in
Confirmation of embryo viability
Embryo viability detected using the detection of a marker in the embryo culture medium is assessed by determining the rate of pregnancy outcomes using a modification of the techniques described by Roudebush et al. (2002), the entire contents of which is incorporated herein by reference.
Embryos generated for IVF are individually assessed for their ability to secrete p53 into the culture medium, as described in previous examples. Embryos thus assessed are transferred into subjects using standard IVF procedures, and the rate of pregnancy which results is correlated with the level of expression of p53 released by the embryo into the culture medium.
Using the data generated by such a study, a threshold level of marker in the culture medium may be selected which will predict an embryo's viability which will produce a desired rate of resultant pregnancy.
Also provided are kits for the determination of the level of a marker indicative of the developmental potential or viability of the embryo in culture medium, wherein the kits facilitate the employment of methods of the invention. Typically, kits for carrying out a method of the invention contain all the necessary reagents to carry out the method. For example, in one embodiment the kit may comprise a first container containing an antibody raised against p53 or Cav1.2 or catalase and a second container containing a conjugate comprising a binding partner of the antibody, together with a detectable label.
Typically, the kits described above will also comprise one or more other containers, containing for example, wash reagents, and/or other reagents capable of quantitatively detecting the presence of bound antibodies. Preferably, the detection reagents include labeled (secondary) antibodies or, where the antibody raised against p53, or Cav1.2 or catalase is itself labeled, the compartments comprise antibody binding reagents capable of reacting with the labeled antibody.
In the context of the present invention, a compartmentalized kit includes any kit in which reagents are contained in separate containers, and may include small glass containers, plastic containers or strips of plastic or paper. Such containers may allow the efficient transfer of reagents from one compartment to another compartment whilst avoiding cross-contamination of the samples and reagents, and the addition of agents or solutions of each container from one compartment to another in a quantitative fashion. Such kits may also include a container which will accept the test sample, a container which contains the antibody(s) used in the assay, containers which contain wash reagents (such as phosphate buffered saline, Tris-buffers, and like), and containers which contain the detection reagent.
Typically, a kit of the present invention may also include instructions for using the kit components to conduct the appropriate methods.
Methods and kits of the present invention may be equally applicable to any animal, including humans, for example including non-human primate, equine, bovine, ovine, caprine, leporine, avian, feline, canine and murine species. Accordingly, for application to different species, a single kit of the invention may be applicable, or alternatively different kits, for example containing reagents specific for each individual species, may be required.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2006902064 | Apr 2006 | AU | national |
