Chromatin Morphology in Human Germinal Vesicle Oocytes and Their Competence to Mature in Stimulated Cycles.

The study was conducted at the Clinical Institute of Reproductive Medicine (Yekaterinburg, Russia) between 2021 and 2022, where the actual work with patients and GV oocytes was carried out from May to August 2021. Patients applied to the clinic for infertility treatment using ARTs. The infertility factors in the analyzed IVF treatments are presented in Supplement (Figure S1 ). The average clinical parameters of the patients whose oocytes were retrieved are shown in Table S1 . All women were of Caucasian (Eurasian) race, various ethnic groups inhabiting the Russian Federation, as well as various social strata without restrictions. For patients, there were no restrictions on age or the level of AMH and FSH. Inclusion parameters were the presence of own (autologous) oocytes after a puncture, the appointment of ICSI by the attending physician, and the presence of one or more GV oocytes after denuding. The material of GV oocytes used in this study was intended for disposal and not for use in IVF programs. The study used all retrieved GV oocytes not intended for ART. One hundred and thirty-five oocytes retrieved from sixty-four patients were included in this study. Each oocyte was perceived as a case. All oocytes were divided into three groups: Group I ( n = 90 from 55 patients)—GV oocytes that spontaneously resumed meiosis in vitro and completed the first meiotic division; Group II ( n = 14 from 12 patients)—GV oocytes that resumed maturation but stopped developing at metaphase I (MI arrest); Group III ( n = 19 from 14 patients)—GV oocytes that stopped before the onset of GV breakdown (GVBD arrest). Oocytes from the same patient may fall into different groups. Thirty-two randomly selected oocytes of the Groups I and II (MI and MII) were used for FISH ( Figure 1 ). All patients had a history taken prior to ovarian stimulation. The level of anti-Müllerian hormone (AMH) was measured in venous blood using a miniVIDAS device (Biomerieux, Craponne, France); the levels of follicle-stimulating hormone (FSH) and thyroid-stimulating hormone (TSH) were measured using an Access device (Beckman Coulter, Inc., Brea, CA, USA) to the manufacturer’s recommendations. Patients were stimulated with gonadotropin-releasing hormone (GnRH) agonist and antagonist protocols. Total dose of gonadotropins were ≥1500 IU. When three or more dominant follicles reached 17–18 mm, patients were administered with ovulation triggers: human chorionic gonadotropin (hCG) (Ovitrelle, Merck Serono, Darmstadt, Germany; Pregnyl, Organon Jersey City, NJ, USA) or, if there were 15 or more dominant follicles, GnRH agonist (Decapeptyl, Ferring Pharmaceuticals, Saint-Prex, Switzerland; Diphereline, Ipsen Pharma, Paris, France). Transvaginal follicle puncture was performed using 17 G aspiration needles 36 h after trigger injection, under intravenous anesthesia (Propofol), using a vaginal transducer with a U/S control. The material was collected in 5 mL syringes. Each follicle was washed separately in 2 mL of Modified HTF medium with HEPES (FUJIFILM Irvine Scientific, Santa Ana, CA, USA). During puncture, before aspiration of the contents, follicles were measured and ranked according to their diameter: large (≥18 mm), medium (16–17 mm), and small (≤15 mm) [ 31 ]; the retrieved cumulus-oocyte complexes were placed in separate marked dishes. Oocytes were removed from the cumulus-oocyte complexes under a microscope in a laminar box with a built-in heating surface under aseptic conditions at 37 °C, washed from blood and follicular fluid in a MHM culture medium (Multipurpose Handling Medium Complete, FUJIFILM Irvine Scientific, Santa Ana, CA, USA) for working with gametes and embryos outside the incubator and then placed in human tubal fluid complete medium (HTF) (FUJIFILM Irvine Scientific, Santa Ana, CA, USA) in a CO 2 incubator (6.0% CO 2 , 37 °C) for 2 h before further manipulations. After 2 h of preincubation in HTF medium, oocytes were denuded using sterile capillaries (140 and 170 μm in diameter) by pipetting in 80 IU/mL hyaluronidase (Irvine, USA) in accordance with the recommendations of the culture media manufacturer. After three-fold washing in MHM, the stage of oocyte development was assessed under a Nikon Ti microscope (Nikon Instruments, Tokyo, Japan) equipped with a relief contrast system. Oocytes accompanied by one PB were evaluated as stage MII oocytes [ 32 ] and further used for fertilization according to the patient’s treatment protocol. Oocytes without a PB and with an intact nucleus (GV) were used for further scientific purposes in this study. GV oocytes in a HTF medium without growth factors were placed in a CO 2 incubator in culture dishes with microwells (EmbryoScope, Vitrolife, Göteborg, Sweden), and time-lapse microscopy (1 frame/10 min) was performed for the subsequent 48 h. The following morphological parameters were assessed: the central or peripheral position of the GV [ 18 , 33 ] ( Figure 2 ) and the level of chromatin condensation/aggregation on the ANu surface [ 13 , 14 ]. According to the degree of chromatin condensation, oocytes were divided into three classes—A, B, and C ( Table 1 ). Oocyte morphometry was performed in glass-bottom dishes (WilCoDish, WillCo Wells B.V., Amsterdam, The Netherlands) 38 h after the trigger of ovulation administration and immediately after oocyte denuding, with the use of an inverted microscope Nikon Eclipse Ti-U, T-P2 polariser (Nikon Instruments, Tokyo, Japan), equipped with a 40×/0.60 DIC Plan Fluor objective. Oocytes were captured three times using a cytometric software package (OCTAX EyeWare Imaging Software, v. 2.2.3.327, Vitrolife, Göteborg, Sweden). The following morphometric parameters were measured: long diameter (D o , μm); short diameter of the oocyte (d o , μm); minimum and maximum thickness of zona pellucida (ZP min /ZP max , μm) ( Figure A1 — Appendix A ). The oocyte projection area (S o , μm 2 ) was calculated as the ellipse area using the formula: S o = π × D o × d o /4 (1) The average oocyte diameter (D av , μm) was calculated as the arithmetic mean between the D o and d o values. The oocyte radius (R o , μm) was calculated using the formula: R o = D av /2 (2) Morphometric measurements of GVs and ANu–chromatin complexes (karyospheres) were performed using JMicroVision v. 1.2.7 software tool (Geneva, Switzerland). Calibration of the software product was carried out using a reference object (1-mm scale, Nikon Instruments, Tokyo, Japan). The following morphometric parameters were measured: the projection area of the nucleus (S GV , μm 2 ); the karyosphere projection area (S k , μm 2 ); the ANu projection area (S ANu , μm 2 ); the minimum distance from the nuclear envelope to the oolemma (L, µm). Several additional parameters, including the diameter of the nucleus (D GV , µm), the radius of the nucleus (R GV , µm), relative eccentricity (L ecc , %), and chromatin projection area (S ch , μm 2 ), were calculated as follows: D GV = 2 × √S GV /π, (3) R GV = √S GV /π, (4) L ecc = 100 × (R o − R GV − L)/(R o − R GV ), (5) S ch = S k − S ANu (6) The morphometry of the chromatin-ANu complex was carried out at the following intervals after the trigger of ovulation: 38 h (immediately after denuding), 44 h (i.e., 6 h after denuding), and 56 h (i.e., 18 h after denuding). To assess the oocyte morphodynamical points during the maturation, the following indicators were evaluated: onset of GVBD (T GVBD ) and extrusion of the PB1 (T PB1ex , min). To evaluate aneuploidy rates in immature oocytes, we performed a biopsy of the karyoplasts containing the first meiotic spindle (MI). The steps of the biopsy procedure are illustrated in Figure A2 ( Appendix A ). Then, to assess aneuploidy rates in mature oocytes (MII), we performed a simultaneous biopsy of the karyoplasts containing the second meiotic spindle and the PB1. Biopsies were performed with 15-µm micropipettes in a mHTF culture medium buffered with HEPES containing 10% HSA and 5 µg/mL cytochalasin B (Sigma-Aldrich, Burlington, MA, USA; Merck Serono, Darmstadt, Germany) as an actin polymerization inhibitor. A laser system (OCTAX, Vitrolife, Göteborg, Sweden) was used for assisted dissection of the ZP. DIC optics was used for imaging. Fixation of the karyoplasts and PBs was carried out on glass slides under a phase contrast microscope. The karyoplasts and PB1 were briefly placed in a hypotonic solution (0.6% BSA and 1% sodium citrate, Sigma-Aldrich, Burlington, MA, USA; Merck Serono, Darmstadt, Germany), then transferred on a glass slide in a minimum volume of the solution. After complete drying, one to two small drops of fixing solution (1:3 mixture of acetic acid and methanol, Sigma, Burlington, MA, USA; Merck Serono, Darmstadt, Germany) were applied. The Vysis MultiVysion PB Multi-color Probe kit (Abbott, Abbott Park, IL, USA) was used to identify common aneuploidies ( Table 2 ). The number of copies of chromosomes was estimated by the number of FISH fluorescent signals using a Leica DM4000B fluorescent microscope (Leica Microsystems, Wetzlar, Germany) equipped with red (600–690 nm), green (500–580 nm), aqua (400–440 nm), blue (420–500 nm), and gold (540–550 nm) filters (Chroma Technology Corporation, Bellows Falls, VT, USA), and a 100× objective. Fluorescent signals were counted in the MI spindle or jointly in the PB1 and the MII spindle (PB1/MII). In MI, the number of fluorescent signals in each chromosome equal to 4 was taken as normal; in PB1/MII, the number of fluorescent signals 2/2 was also taken as normal. The variants 3/1, 1/3, 0/4, and 4/0 were considered chromosome segregation errors. Fluorescent signal variants in MI equal to 0 or 2 were taken as a chromosome aggregation error (loss of chromosomes). Fluorescent signal variants 1/1, 2/0, 0/2, and 0/0 in PB1/MII were suggested as a chromosome aggregation error (loss of chromosomes). If segregation errors were detected for some chromosomes and aggregation errors for others, then a conclusion was made about a combined error. Qualitative features were described by simply indicating the number of patients and the proportion (in percent) for each category. The statistical significance of differences between these features was assessed using the χ 2 test with Yates correction and Fisher’s exact test. All quantitative parameters were tested for normal distribution using the Shapiro–Wilk test. Taking into account that the distribution of some quantitative parameters was significantly different from the normal one, statistical analysis was carried out using nonparametric criteria. The values are described as a median and boundaries of the interquartile interval (25–75%). The statistical significance was assessed using the Mann–Whitney test. The differences were considered statistically significant at p < 0.05 in all cases.

The process of oocyte development includes two-stage meiotic division, resulting in the formation of haploid female gametes ready for fertilization and further zygote development [ 1 ]. The diplotene stage of meiotic prophase—at which the oocyte nucleus is called the germinal vesicle (GV) [ 2 ]—is crucial for the oocyte to transit from growth to maturation. Oocyte maturation is a complex process in which cytoplasmic and nuclear factors contribute [ 3 ]. After the GV stage and the germinal vesicle breakdown (GVBD), two meiotic stages are the key waystations of oocyte maturation— metaphase I (MI) accompanied by the emission of the first polar body (PB1) and metaphase II (MII) determined by the release of the second polar body (PB2). Each stage is equally important for the oocyte as it allows the female gamete to attain an optimal state of developmental competence [ 4 ]. However, it is at the GV stage that the oocyte primarily acquires the capacity to be fertilized and further develops properly into a future embryo [ 5 ]. Both nuclear and cytoplasmic factors and structures substantially involved in oocyte maturation should be created, accumulated, and integrated into further developmental events [ 6 ]. Some determinants affecting meiotic progression have already been elucidated, while other factors associated with the developmental arrest at the GV stage have yet to be defined [ 7 , 8 ]. The GV is characterized by global chromatin rearrangements at both morphological and molecular levels [ 9 ]. In some mammals, including humans, chromatin rearrangements within the GV coincide with the transformation of the nucleolus into a transcriptionally inert nuclear body called the nucleolus-like body (NLB) or, more recently, the atypical nucleolus (ANu) [ 10 ]. In this case, the condensed chromatin forms at the ANu periphery a more or less compact perinucleolar ring, sometimes called a karyosphere [ 11 , 12 ]. There is no universal classification of chromatin configuration in human GV oocytes. The main architectural patterns of chromatin found in human GVs are the following [ 13 , 14 ]: (i) no karyosphere (peri-ANu ring) is observed, chromatin is dispersed through the GV, and only some heterochromatin blocks are located both in the vicinity of the ANu and outside; (ii) the ANu is incompletely rimmed by chromatin; (iii) the ANu is completely surrounded by chromatin, but some chromatin masses are scattered outside the peri-ANu rim; (iv) all chromatin surrounds the ANu in the GV, forming a compact well-formed karyosphere. Approximately 50% of human oocytes retrieved from antral follicles have rather condensed chromatin [ 15 ]. During the GVBD and the emission of the PB1 and PB2, the processes of repositioning and remodeling of organelles occur, including mitochondria, the Golgi complex, and the endoplasmic reticulum [ 6 , 16 ]. This has been vividly demonstrated using a modern time-lapse technique [ 17 ]. The functional significance of such rearrangements during oocyte maturation is not completely clear. It is assumed that changes in the oocyte structure play a role in the maturation and further development of the embryo. For example, the central position of the GV in both mouse [ 18 ] and human oocytes [ 19 ] correlates positively with the tendency of the oocyte to resume meiosis and depends on the functional state of the cytoskeleton [ 20 ]. Currently, there is no unified method for assessing the initial quality and development potential of GV oocytes and subsequent embryos. However, such an integrated approach would be useful to course the prospects for infertility treatments. Along with the morphological parameters of mature oocytes at the metaphase II (MII) stage, some changes in the parameters of GV oocytes—e.g., a number of immature oocytes—can probably serve as a criterion for assessing the quality of response to hormonal stimulation [ 21 ]. A fully developed GV oocyte is capable of spontaneous maturation to MII when isolated from follicles >3 mm [ 22 ]. The levels of implantation and quantity/quality of blastocysts for in vitro matured oocytes, both in the stimulated cycle (GV rescue) [ 23 ] and classical non-stimulated IVM [ 24 , 25 ], were found to be lower compared to a conventional IVF cycle. The low percentage of oocytes matured in vitro and the poor quality of further embryos indicate that a significant proportion of oocytes retrieved from antral follicles are meiotically incompetent. It is likely that GV oocytes with more compacted chromatin are more capable of developing. For example, porcine oocytes with a fully developed karyosphere are better suited for IVF after in vitro maturation [ 26 ]. Contrariwise, mouse GV oocytes with predominantly diffuse chromatin can fertilize, but the descendant embryos cannot reach the blastocyst stage in vitro [ 27 ]. Moreover, human oocytes with a similar chromatin pattern show some ultrastructural signs of cytoplasmic degeneration [ 28 ]. It has been experimentally shown that chromatin remodeling defects in oogenesis also cause aneuploidies, leading to pre- and post-implantation developmental arrest, implantation disorders, and spontaneous abortions [ 29 ]. Such widely-used morphological and morphometric indicators as the state of the nucleoplasm, the position of the GV, the shape of the nuclear envelope, and the size of the oocyte are associated with chromatin condensation [ 30 ]—a potential marker of oocyte quality in IVM cycles. Here, we performed a prospective cohort study of GV oocytes retrieved from patients treated for infertility with IVF. The aim of this study was to reveal whether the morphology of the chromatin compartment correlates with the capability of GV oocytes to resume meiosis.

A comparative analysis of the ability of GV oocytes to resume maturation and develop to the MII stage was performed, taking into account the collected history of patients. All oocytes were divided into three groups according to their ability to resume meiosis ( Figure 1 ). Anamnestic data for different groups of oocytes are summarized in Table 3 . Patients whose oocytes cease to develop at stages MI and GV (Groups II and III, respectively) significantly differ in age. There are also significant differences between Groups I and III in the AMH level in the blood, which reflects differences between the capacity of oocytes to complete a full cycle of maturation, including resumption and completion of meiosis to MII and the tendency of oocytes to stop development at the GV stage ( Table 3 ). Significant differences are found in the competence of oocytes to initiate meiosis and extrude the PB1 in the following groups of patients: (i) with polycystic ovary syndrome (PCOS), more common in Group II than in Group I; (ii) with endometriosis, more common in Group III than in Group I; and (iii) after ovarian resection, which was significantly less common in Group III with GV-arrested oocytes compared with Group I with complete meiosis. While ovarian resection in Group I is a fairly common event, no cases were noted in Group III. Among the compared groups of patients, there are no significant differences in body mass index (BMI), the number of antral follicles, FSH and TSH levels, type of infertility (primary or secondary), and premature ovarian failure (POF) ( Table 3 ). To assess the effect of hormonal stimulation on the ability of oocytes to mature spontaneously, we evaluated the stimulation protocols and ovulation triggers, as well as the drugs purchased from different manufacturers, which were used in different groups of patients ( Table 4 ). In Group I, a short gonadotropin-releasing hormone (GnRH) antagonist protocol was used more frequently, but the differences were not significant. No differences were found between Groups I/II and Group III when human chorionic gonadotropin (hCG) or GnRH agonists were used as triggers, either. Further, no significant differences were found in patients treated with the same drug supplied by different manufacturers. To assess the adequacy of the ovarian response to hormonal stimulation, we monitored the estradiol level (E 2 ) in the blood on the day of transvaginal aspiration ( Table 5 ). In other words, we tested how actively the ovaries respond to the growth of dominant follicles in FSH-stimulated patients. Despite a wide range observed, no significant differences are found. Other characteristics of clinical response to stimulation are also presented in Table 3 . No significant differences are detected in the number of dominant follicles per puncture, the number of received oocytes, the number of GV and mature oocytes, the quality of the embryos received on days three and five in cycles, and clinical pregnancy rates (CPR). All GV oocytes were retrieved from the medium (16–17 mm) and small (≤15 mm) follicles. Larger follicles that contain mature oocytes (MI and MII) were not used in this study. Follicle size does not differ significantly in different groups/subgroups of patients. The percentage of GV oocytes retrieved, respectively, from small and medium follicles is shown in Figure 3 . The representative oocytes with central and peripheral positions of the GV are shown in Figure 2 . Although the central position of the GV was somewhat more common in Groups II and III, the studied groups do not differ significantly by this parameter, regardless of whether the qualitative assessment of the GV (central or peripheral) was performed or the relative displacement of the GV (L ecc ) was calculated as described in Section 2 ( Figure 4 a,b). Large-scale morphometric data are presented in Table 6 . In all groups, GV oocytes did not differ significantly in size. However, Groups II and III showed little difference in the length of the oocyte long axis (D o ), but the calculated average oocyte diameter (D av ) and oocyte projection area (S o ) do not differ significantly. In all the studied groups, there were no significant differences in the thickness of z. pellucida (ZP min /ZP max ). The nucleus projection area (S GV ) and the calculated diameter of the nucleus (D GV ) were larger in Group III; the differences are significant between Groups I and III but not between Groups II and III. Using time-lapse microscopy, we estimated the time until the onset of GVBD (T GVBD ). This period was longer in Group II than in Group I ( Table 7 ). Among all GV oocytes that entered and finished maturation, the time from the onset of GVBD to the emission of the PB1 (T PB1ex ) was approximately 16.5 h (995.0 min), and time was scattered minimally in this case. The chromatin configuration in GV oocytes has attracted special attention in this study. Using DIC microscopy, we were able to differentiate three main types of chromatin configuration, referred to as Classes A, B, and C ( Figure 5 and Table 1 ). There was no case when the projection area of chromatin aggregated on the ANu (S ch ) was equal to zero µm, indicating that the retrieved dominant follicles contained oocytes with different levels of heterochromatin aggregation at the ANu surface. Although at least one prominent heterochromatin block was always seen adjacent to the ANu, we observed different chromatin patterns, which are the closest to those observed in Classes A, B, and C oocytes according to the classification proposed by Miyara et al. [ 14 ], see also Table 1 . At the same time, we were unable to distinguish chromatin masses in the nucleoplasm from the “threads of dispersed chromatin” characteristic for Class D oocytes, according to Combelles et al. [ 13 ]. In our material, Class C oocytes were the most common, while Class A oocytes were the rarest ( Figure 6 a). The percentage of oocytes with different degrees of chromatin compaction is shown in Figure 6 b. Class B and C oocytes were more frequently detected among the oocytes capable of complete maturation. The oocytes that entered maturation but were arrested at the MI stage more often belonged to Class A. The oocytes that did not enter maturation were more often classified as Class A. At the same time, the comparison groups did not show significant differences concerning the Class C oocytes. Contrarily, oocytes significantly differ in Groups I and III by the Class B chromatin configuration. Finally, there are significant differences between Groups I and III and between Groups I and II by the presence of Class A oocytes, but Groups II and III do not differ significantly ( Figure 6 b). The parameter S ch showed some differences in the studied groups of oocytes, demonstrating a significantly reduced S ch in Group III compared with Group I ( Figure 7 a). The ANu projection area (S ANu ) is significantly larger in the oocytes of Group II than in the oocytes of Groups I and III ( Figure 7 b). The level of chromatin aggregation on the ANu surface changes during in vitro culture of GV oocytes in classes B and C. The parameter S ch noticeably increased in these oocytes already after 6 h of cultivation, expanding even more by 18 h ( Figure 8 a). In Class A oocytes, S ch also tends to increase, but the differences are not significant ( Figure 6 a). The ANu projection area (S ANu ) is not influenced significantly during the cultivation of GV oocytes in vitro ( Figure 8 b). Since we confirmed the possibility of GVBD and MI spindle formation in oocytes with an incomplete karyosphere (Class A), we assumed that, in this case, an incomplete spindle is formed. Such a spindle, which apparently does not unite all chromosomes, leads to the loss of chromosomes and pre-segregation aneuploidy. To investigate this, we dissected ZP with a laser, after which the karyoplasts containing MI and a small amount of ooplasm as well as the karyoplasts containing MII together with PB1 were isolated ( Figure A2 — Appendix A ), and then stained with locus-specific (LSI) and centromeric (CEP) fluorescent probes ( Figure 9 ). High aneuploidy rates were found in oocytes of all classes ( Figure 10 a). In Class A oocytes, which have the lowest chromatin aggregation, the frequency of aneuploidy seemed to be slightly higher than in Class B and C oocytes, but these differences are not statistically relevant. As for the source of aneuploidy, segregation errors are the main cause of aneuploidy in Class B and C oocytes, while aggregation errors and a combined cause lead to aneuploidy in Class A oocytes. Statistically significant differences were found between Class A and Class B/C configurations, but only for aneuploidy caused by aggregation errors ( Figure 10 b).

Our study was devoted to the search for new predictors of oocyte quality, as it is important to increase the percentage of successful outcomes in ARTs [ 21 ]. Older reproductive age and a low AMH level are traditionally considered unfavorable anamnestic factors, probably due to a decrease in the number of available oocytes and disturbances in the regulation of the growth and maturation of follicles [ 34 ]. In addition, endometriosis reduces the prognosis of successful IVF programs [ 35 ] and, as shown in our study, can reduce the quality of oocytes by affecting their maturation during meiotic prophase. At the same time, we have documented that the initial number of antral follicles before the start of the cycle, as well as body mass index and the cause of infertility, are not significant factors. Neither the stimulation protocol chosen for ovarian superovulation nor ovarian responses are predictive of spontaneous activation of GV oocytes. Moreover, the ability of oocytes to resume meiosis does not correlate with the embryonic and clinical outcomes of the forthcoming infertility treatment program. The possibility of using immature (GV and MI) oocytes in in vitro fertilization (IVF) programs is recurrently discussed [ 36 ]. The use of GV oocytes for IVF results in an increase in the average number of available MII oocytes, one additional blastocyst per cycle, and, finally, a higher live birth rate [ 23 , 37 ]. The use of immature oocytes obtained after hormonal stimulation followed by in vitro maturation (IVM) is called the GV rescue [ 23 ] and can be considered as an additional assisted reproductive technology (ART) if the number of mature oocytes retrieved during IVF is incomparably less than expected as determined by folliculometry. Successful rescue in vitro maturation (IVM)−ICSI performed shortly after PB extrusion was previously reported, resulting in a successful pregnancy and birth of a healthy baby by a patient who had no mature oocytes at the time of oocyte retrieval [ 38 ]. One of the few previous studies on human GV oocytes has demonstrated a relationship between follicle diameter, oocyte size, and morphology of the chromatin compartment [ 14 ]. Another study [ 15 ] showed that GV oocytes obtained in stimulated IVF cycles significantly exceed the size of those oocytes that are not capable of resuming meiosis after IVM cycles. In our study, we used only GV oocytes from dominant follicles (small and medium), which stopped their growth and no longer increased in size. We found no differences in the study groups in terms of follicle and oocyte size, GV position, and ZP thickness. This is consistent with previous works [ 18 , 33 ], which found no relationship between GV position and the quality of human oocytes, despite the fact that such a relationship was shown for mouse oocytes [ 20 ]. At the same time, we were able to demonstrate a reliable relationship between the state of the heterochromatin compartment and the ability of GV oocytes to resume meiosis and complete maturation. A low level of chromatin condensation (Class A oocytes) correlates negatively with the ability of the oocyte to resume meiosis, while an intermediate level of chromatin condensation in oocytes containing an incomplete peri-ANu rim (karyosphere) and numerous additional heterochromatin blocks in the nucleoplasm (Class B oocytes) correlates positively [ 13 , 14 ], therefore suggesting that the degree of chromatin condensation in human GV oocytes can be considered as a valuable predictor of spontaneous maturation in stimulated cycles. However, Class C oocytes that exhibit a fully formed karyosphere, when all the chromatin rims the ANu [ 11 ], displayed no significant correlation with spontaneous maturation—probably, due to some unconsidered factors. Chromatin was the most dynamic in Class B oocytes cultured in vitro for 6 and 18 h. In Class C oocytes, however, chromatin is less dynamic, which may be linked with the cessation of general transcription activity towards the end of the GV stage [ 11 ]. The main cause of pre- and post-implantation arrest of embryo development and spontaneous abortions are aneuploidies resulting from disturbances in the segregation of homologous chromosomes and sister chromatids during maturation of the oocyte after GVBD, at stages MI and MII, respectively [ 39 , 40 ]. It was interesting to examine how the incomplete process of karyosphere formation—chromatin aggregation on the ANu surface—affected the level of pre-segregation and segregation aneuploidies. Using LSI and CEP probes for FISH, we found that GV oocytes with a low level of chromatin condensation exhibit a higher level of aneuploidy upon resumption of meiosis, suggesting that abnormal chromatin aggregation at the GV stage may contribute to the occurrence of aneuploidy. In oocytes with a high level of chromatin condensation, the most common cause of aneuploidy is chromosome segregation errors. The mechanisms causing aneuploidy at this stage have not yet been studied in detail. There are quantitative data on aneuploidy in oocytes that have undergone spontaneous maturation and subsequent activation, obtained by FISH and regarding different levels of chromosome aggregation, but data on the source of aneuploidy were not presented [ 22 ]. The existence of a pre-segregation source of aneuploidy is currently being discussed [ 41 ]. An aneuploid set of chromosomes was documented in GV oocytes, accounting for 20% of all cases of aneuploidy [ 42 ]. In another study, using microarray comparative genomic hybridization, approximately 15% of GV and MI oocytes exhibited such aneuploidies, the putative cause of which is gonadal mosaicism [ 43 ]. In our opinion, disturbances at the stage of chromatin aggregation in GV oocytes, leading to the appearance of aneuploid MI oocytes after GVBD, are also not excluded. The study of the mechanisms linking chromatin condensation and the incidence of aneuploidy was not within the scope of this study. Nevertheless, we can assume that the condensation of chromatin around the atypical nucleolus and the formation of the karyosphere contribute to the spatial organization of meiotic chromosomes. Impaired formation of the karyosphere, including due to impaired expression of key heterochromatinization proteins, can lead to an increase in the frequency of errors in chromosome behavior during meiotic divisions and, as a result, to the formation of aneuploid oocytes/embryos, as shown, for example, for mice with impaired expression of chromatin remodeling protein ATRX [ 29 ]. As for the ANu, it apparently makes a significant contribution to maintaining the integrity of the genome during meiotic divisions, as well as the first divisions of cleavage. However, from our point of view, the ANu plays a role only as a scaffold for chromosomes in their spatial organization. It is difficult to believe that nucleolar transcription plays a significant role in these processes since by the end of the diplotene of female meiosis, the nucleoli turn into transcriptionally inactive homogeneous fibrillar structures—NLBs/ANu [ 44 , 45 , 46 , 47 , 48 ]. Summarizing, the main conclusion of our study is that human GV oocytes that are not capable of successfully completing meiosis display predominantly a low level of chromatin assemblage into a karyosphere. Given that the level of chromatin condensation can be determined in vivo using light microscopy, we believe that this morphological characteristic can be considered a promising criterion for selecting GV oocytes of the best quality in rescue IVM programs.