Background

Cancer survival in girls and young women has significantly improved; however, radiotherapy and chemotherapy may alter ovarian function by reducing the primordial follicle reserve. As a result, patient fertility may be impaired and premature ovarian failure (POF) may occur [1-3]. Therefore, techniques for female fertility preservation have been developed, including oocyte, fertilised embryo, and ovarian tissue preservation [2,4]. To date, ovarian tissue preservation remains the optimal procedure for prepubertal girls who, after cancer remission, may be auto-transplanted when the desire for pregnancy arises.

Adult ovarian tissue cryopreservation and transplantation techniques have been successfully performed and have resulted in the birth of 30 children [5,6]. However, this procedure still needs to be optimised because significant follicular loss has been observed during cryopreservation and subsequent grafting [7,8]. Grafting whole ovaries cryopreserved with vascular anastomosis may prevent follicle loss through ischemia. However, this method suffers from a number of drawbacks including a difficult cryopreservation process, a laborious surgical technique, which does not always prevent ischemic damage, and the possibility of reintroducing malignant cells [9,10]. The most important challenges in the transplantation of cryopreserved ovarian fragments are tissue ischemia and reperfusion injury [11,12]. Transient hypoxia during the first 5 days after ovarian tissue transplantation is followed by gradual oxygenation recovery, which is associated with restored angiogenesis and reperfusion over the next 5 days [13,14].

A reduction in post-transplantation hypoxia and subsequent follicular loss could significantly improve ovarian graft efficiency. Therefore, angiogenic factors have been tested in cryopreservation and xenotransplantation models. Sphingosine-1-phosphate (S1P) is a sphingolipid metabolite that decreases apoptosis and stimulates angiogenesis and endothelial cell migration. S1P promotes neoangiogenesis in ovarian transplants and reduces ischemic reperfusion injury during the days following transplantation in a xenograft mouse model [15]. In addition, the use of erythropoietin (EPO) was found to improve early follicle morphology and stromal cell density in canine ovarian transplants after 8 weeks and to enhance blood vessel density 16 weeks after xenografting in severe combined immunodeficient (SCID) mice [16].

The use of growth factors to improve ovarian tissue survival after grafting has progressed beyond the preclinical stage. Callejo et al. reported the first human live birth after impregnation with the frozen/thawed ovarian cortex of the patient and platelet-rich plasma (PRP) [17]. Therefore, it is important to precisely delineate the cytokines that may convey a significant clinical advantage to ovarian grafting efficiency.

Vascular endothelial growth factor (VEGF), specifically VEGF-A, is a potent angiogenic factor that stimulates vascular endothelial cell survival, proliferation, migration, and differentiation. Moreover, some data suggest that VEGF-A appears to be involved in folliculogenesis with the presence of VEGF-A receptors in granulosa cells [18]. VEGF is a disulfide-bonded dimeric glycoprotein that is encoded by a gene that contains 8 exons. VEGF acts mainly through binding to VEGF receptor-2 (VEGF-R2) but also binds to VEGF receptor-1 (VEGF-R1). In addition, alternative splicing creates numerous isoforms, mainly VEGF121, VEGF165, and VEGF189. VEGF165 (containing exons 1–5, 7, and 8) is secreted as covalently linked homodimers of 45 kDa with a basic character and moderate affinity for heparin. VEGF165 can be found in many tissue types in a soluble form or anchored to the extracellular matrix, and a minimal amount of matrix-bound VEGF165 can support endothelial cell growth [19-22]. We previously demonstrated the beneficial effect of VEGF111, a highly soluble and diffusible VEGF isoform, in an original model of ewe ovarian tissue xenografts in SCID mice. VEGF111 lacks exons 5–7 and is resistant to proteolysis [20]. The use of this isoform in a collagen matrix, which encapsulates the ovarian cortex at the time of transplantation, was found to improve angiogenesis and decrease hypoxia, thereby enhancing the preservation of primary follicles [23].

For this study, sheep ovarian cortex was used due to ethical barriers and the limited availability of human ovarian tissue. Sheep ovary is an adequate candidate for research due to its ovarian architectures (which are similar to those of human ovarian tissue), limited number of developed follicles and single ovulation with primordial follicles distributed superficially in the cortex. Its size is 80% of that of the human premenopausal ovary, and it has a comparable collagen-dense cortical layer containing the pool of primordial follicles [24]. The sheep ovary has been used in many studies [7,25-28].

In this study, using the same xenograft model, we tested whether VEGF165, which, unlike isoform 111, is anchored to the extracellular matrix, could improve ovarian graft survival by extending the exposure of the ovarian fragment to this cytokine through sustained release from collagen.

Methods

Ovarian tissue sampling

The ethics committee of the University of Liège approved the present study (reference 1156, February 2011). Study was initiated in March 2011 and terminated in October 2013.

Five ewes (10 ovaries) were obtained from the Ovine Research Centre (University of Namur, Belgium). Veterinary euthanised ewes were intravenously injected with T61 1 ml/Kg (MSD, Belgium), a laparotomy was performed, and ovaries were sampled immediately. The ovaries were placed in Leibovitz L-15 medium (Lonza, Basel, Switzerland) supplemented with 10% normal sheep serum (Hormonology Laboratory, Belgium) and kept at 4°C during transport (approximately 1 hour (h)) and during the preparation (approximately 1 h) of cortical fragments.

Cryopreservation and thawing processes

As previously described [29], ovarian cortical fragments were prepared by cutting the cortex into pieces (2.5 × 2.5 × 1 mm) after the medullar tissue was resected. These ovarian strips were equilibrated in cryopreservative medium that contained Leibovitz L-15 medium, which was supplemented with dimethyl sulfoxide 1.5 M (DMSO) (Sigma), 10% normal sheep serum, and 0.1 M sucrose for 30 min at 4°C. They were transferred into cryovial tubes (Simport Scientific, Canada) containing the same medium. The tubes were cooled in a programmable freezer (CL-8800i System, Cryologic Pty., Ltd., Australia) and stored in liquid nitrogen [25]. Ovarian samples were stored in cryotubes for several weeks to several months until transplantation into mice (minimum 2 weeks, maximum 6 months). The cryovial tubes were kept at room temperature (RT) for 2 min to thaw and then immersed in a 37°C water bath until the frozen media melted, approximately 2 to 3 min. After thawing, the ovarian strips were given three 5 min washes at 37°C in Leibovitz medium to remove the cryoprotective agents.

Ovarian transplant encapsulation and SCID mouse transplantation

Ewe ovarian cortical strips were encapsulated in a three-dimensional type I collagen (Col I) matrix with or without VEGF165 as previously described [23] and illustrated in Figure 1. Collagen matrix was prepared by mixing 9 volumes of Col I (2.4 mg/ml) extracted from rat tail tendons [30], 1 volume of 10X minimal essential medium (Life Technologies, Belgium) and approximately 0.1 volume of 1 M NaOH to adjust the pH to 7.4 (Figures 1A-B). Agarose rings (1.5% Agarose VII solution, Sigma, Belgium) were filled with the first layer of collagen (60 μL) matrix with or without recombinant murine VEGF165 (50 nM, Peprotech, Rocky Hill NJ, USA, Cat N° 450–32). After polymerisation, frozen/thawed ovarian sheep explant (2.5 × 2.5 × 1 mm) was placed and overlaid by a second layer of Col I (60 μL). The agar ring was removed before transplantation in mice (Figures 1C-G).

Figure 1
figure 1

Encapsulation of ovarian graft in collagen matrix with and without VEGF 165 . A. Type I collagen was extracted from rat tail tendons. B. Preparation of collagen matrix. C. Adjusting collagen mix to pH 7.4. D. Illustration of agarose rings. E. Filling of agarose ring with a first layer of the collagen matrix with or without recombinant murine VEGF165. F. Frozen/thawed ovarian sheep explant deposit. G. Second layer of collagen matrix with or without recombinant murine VEGF165. H. Agar ring removal before transplantation.

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Eight-week-old female SCID mice (n = 66, Charles River, Burlington MA, USA) were selected for ovarian xenotransplantation because the SCID affected both B and T lymphocytes (Table 1). After shaving and anaesthesia by intraperitoneal injection of ketamine (100 mg/kg) and xylazine (10 mg/kg), a dorsal incision was performed and a single ovarian cortex, which was encapsulated in collagen gel, was stitched into the right mouse ovary using 7–0 Prolene sutures. To detect functional vessels and possible anastomoses of sheep and mouse vessels in the grafted ovary transplant, 200 μl of dextran-fluorescein isothiocyanate (FITC, 2.5 mg/ml in PBS) (Sigma-Aldrich, Saint Louis, MO, USA) was intravenously injected 3 min before sacrifice. Functional vessels were detected on transplanted sections with anti-fluorescein Ab (Converter-POD, Roche, Penzberg, Germany). The animals were euthanized 3 days or 3 weeks after grafting. Ovarian cortical tissue specimens were recovered and fixed in 4% formaldehyde.

Table 1 Study design
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Histological assessment

Each graft was embedded in paraffin and cut into 5-μm-thick serial sections. Several immunohistochemistries were performed after 3 days or 3 weeks of transplantation (Table 1). Ten sections per transplant, which covered the entire ovarian fragment, were stained with haematoxylin and eosin (H&E) and analysed as previously described to overcome the effect of heterogeneous follicular distribution within the transplanted ovarian cortex [24]. Only follicles in which a defined nucleus was visible were counted and separated into primordial, primary, secondary, or antral follicles according to the classification by Gougeon [31]. In these slices, follicular quality was evaluated and classified as normal or abnormal according to the morphological assessment. As previously described [32-34], the integrity of oocytes, granulosa cells, and basement membrane cells was observed. Follicles were classified as normal when they contained an intact oocyte and granulosa cells or abnormal when they contained a pyknotic oocyte nucleus and a shrunken ooplasm regardless of the presence of disorganised granulosa cells.

The immunohistochemical detection of vascular endothelial cells (CD31), functional blood vessels (dextran-FITC), and mature blood vessels (α-SMA) was performed using specific primary antibodies. Murine vascular blood vessel colonisation in the graft was detected using species-specific CD31 immunostaining. Incubation in PBS-BSA 10%, for 30 min at RT, was used to block non-specific binding sites. CD31 primary antibody (Ab) was diluted 1:100 in PBS-BSA 1% and incubated for 2 hours (h) at RT (Rat anti-mouse, ab56299, Abcam, Cambridge, United Kingdom), followed by incubation with the secondary Ab/HRP (AffiniPure rabbit anti-rat IgG diluted 1:4,000), (JAC-31200504, Lucron ELITechGroup, Puteaux, France) for 30 min at RT. Then, the reaction was revealed using DAB+ (K3468, Dako, Glostrup, Danemark).

Through the Dextran-FITC injection given to mice before sacrificing them, functional blood vessels were observed after immunostaining using an anti-fluorescein Ab (Converter-POD, Roche, Penzberg, Germany). Incubation in PBS-BSA 10%, for 30 min at RT, was used to block non-specific binding sites. This immunostaining was performed in one step by using an anti-fluorescein Ab/HRP ready to use (incubated for 30 min at RT), which directly recognised the FITC molecule fixed on Dextran injected before sacrifice, and the reaction was revealed using DAB+.

Mature functional blood vessels were recognised by double staining with dextran-FITC and α-SMA Abs. Incubation in PBS-BSA 10%, for 30 min at RT, was used to block non-specific binding sites. Staining against dextran-FITC was performed using an anti-fluorescein Ab/HRP ready to use (Converter-POD, Roche, Penzberg, Germany), which was incubated for 30 min at RT, and the reaction was revealed using DAB+. A second non-specific binding sites was blocked, by incubation in PBS-BSA 10% for 30 min at RT, before α-SMA staining was performed using a mouse anti-αSMA/FITC Ab diluted 1:1,000 in PBS-BSA 1% and incubated for 1 h 30 min at RT (F3777, Sigma-Aldrich, Saint Louis, MO, USA), followed by application of the AEC substrate chromogen (K3464, Dako, Glostrup, Danemark). In this double staining procedure, mature functional blood vessels appeared in red (α-SMA) and brown (dextran-FITC).

Fibrosis was evaluated using saffron staining. Incubation was performed for 10 min at 37°C in 1% saffron solution (Microm Microtech, Francheville, France) in absolute ethanol.

Section and fibrosis analysis

Images of whole-tissue sections were digitised at high magnification (100×) to produce virtual images in which the pixel size was 1.510 μm. Vessels and the contour of the whole ovarian grafted tissue were drawn manually for each section. Then, the number of vessels and the surface of the whole tissue were measured automatically. Finally, the number of vessels was determined according to the surface units of ovarian grafted tissue. The image analysis was conducted using MATLAB 7.9 software.

Fibrosis was analysed on the digital images of saffron-stained slices using ImageJ software (National Institutes of Health, USA). Digitised colour images were first decomposed into three components of red, green, and blue. To enhance the features of fibrosis, the blue component was subtracted from the red component. The resulting images were then binarised using an appropriate threshold. With this method, pixels that were associated with fibrosis were assigned a value of 1 and pixels that were associated with the tissue were given a value of 0. The ratio between the surface that was occupied by the fibrotic area and the total surface area of the tissue represented the proportion of fibrotic tissue in each transplant.

Statistical analyses

A statistical analysis was performed using GraphPad Prism software. The Mann–Whitney test was applied for comparisons between the two different groups. The statistical evaluation of the presence of blood vessels (dextran-FITC- or dextran-FITC/α-SMA-positive vessels) and the percentage of morphologically normal or abnormal follicles between the groups was performed using the Fisher’s exact test. Statistical significance was set at p ≤ 0.05.

Results

Vascularisation of ovarian cortical grafts

Vascularisation in ovarian grafts was evaluated following an intravenous injection of dextran-fluorescein isothiocyanate (FITC) solution 3 min before sacrifice. Functional blood vessels in the ovarian transplants were detected after immunohistochemical labelling with FITC (Figure 2A).

Figure 2
figure 2

The analysis of functional blood vessels in ovarian grafts 3 days after transplantation. A. An illustration of functional blood vessels that were observed using dextran-FITC immunostaining. B. The quantification of FITC-positive vessels in ovarian transplants from the control and VEGF165-treated groups. In the treated mice, 8 of 15 fragments contained functional vessels compared with only 4 of 14 fragments in the control mice. C. An illustration of double staining for functional and mature blood vessels in a transplant that was treated with VEGF165. FITC was stained brown, and α-SMA was stained red. n corresponds to the number of transplanted ovarian fragments that contained functional blood vessels. Scale bar: 200 μm. *Corresponds to a p value < 0.05. Error bar are SEM (mean standard error).

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Three days after transplantation

Functional (dextran-positive) blood vessels were detected in 53% of the mice (8/15) in the VEGF165-treated group versus 28.6% of the mice in the control group (4/14) (p = 0.26) (Table 2). In these FITC-positive transplants, functional blood vessel density was determined using semi-automated computer-assisted analysis as previously described [35]. A higher density of dextran-FITC-positive vessels was observed in the VEGF165 group (8.22 ± 2.10 vessels/mm2) compared with the control group (2.45 ± 1.27 vessels/mm2) (p = 0.03) (Figure 2B). To determine whether these functional vessels were mature, double immunostaining against dextran-FITC and alpha-smooth muscle actin (α-SMA) was performed to detect pericytes and/or smooth muscle cells (Figure 2C). Among the FITC-positive xenograft transplants (4/14 in the control group and 8/15 in the VEGF165-treated group), 50% of the transplants in the VEGF165-treated group were positive for α-SMA (4/8). In the control group, no transplants displayed double positivity (0/4) (p = 0.21) (Table 2). Double positivity demonstrated anastomosis between murine and ovine blood vessels, as murine neovessels within the fragment cannot be mature after only 3 days.

Table 2 Number of ovarian transplants showing functional, mature functional and murine blood vessels 3 days after transplantation
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As previously described, vascularisation of xenografted ovarian tissue results from anastomoses between ovarian vessels and host vessels, as demonstrated through previous double staining, and from graft colonisation by murine blood vessels, termed chimeric vessels [36]. The immunodetection of murine CD31 using a species-specific anti-mouse CD31 antibody (Ab) identified blood vessels that had migrated from the murine uterine horn to the sheep ovarian graft 3 days post-transplantation (Figure 3A). A higher proportion of ovarian grafts that contained murine-specific CD31-positive vessels were observed in the VEGF165-treated group (40%, n = 15) compared with the untreated group (21.4%, n = 14), but the difference was not significant (p = 0.43) (Table 2). However, no difference in vessel density was observed between the two experimental groups (0.77 ± 0.28 vessels/mm2 in the VEGF165-treated group versus 0.59 ± 0.41 vessels/mm2 in the control group, p = 0.36) (Figure 3B).

Figure 3
figure 3

- Murine blood vessels in sheep ovarian transplants after 3 days and 3 weeks reflect colonisation by host vessels into the graft. A. An illustration of murine blood vessels that were stained with a mouse-specific CD31 Ab in an ovarian fragment that was treated with VEGF165 and removed 3 days after transplantation. The host tissue is identified by the dotted arrow, and the graft is identified by the plain arrow. B. The quantification of murine blood vessels in the grafted tissue 3 days after transplantation. In the treated mice, 6 of 15 fragments contained CD31-positive blood vessels compared with only 3 of 14 fragments in the control mice. C. The quantification of murine blood vessels in the grafted tissue 3 weeks after transplantation. All of the fragments in both the control and treated groups contained CD31-positive blood vessels. n corresponds to the number of transplanted ovarian fragments that contained murine blood vessels. Scale bar: 200 μm. **Corresponds to a p value < 0.01. Error bar are SEM.

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Three weeks after transplantation

In contrast, 3 weeks after grafting, a higher density of species-specific murine CD31-positive vessels was observed in the VEGF165 group (23.72 ± 14.36 vessels/mm2, n = 18) compared with the control group (9.13 ± 3.45 vessels/mm2, n = 15) (p < 0.01) (Figure 3C).

Fibrosis, follicular density, and morphology

Analysis of fibrosis, evaluated using saffron staining, showed a similar extent of fibrosis in the VEGF165 (53.82 ± 1.45%, n = 18) and control (50.31 ± 1.2%, n = 15) groups three weeks after grafting (p = 0.053) (Figure 4A). The analysis of primordial and primary follicle density in haematoxylin and eosin (H&E)-stained sections 3 weeks after grafting indicated a predominance of primordial follicles in the graft (Figure 4B). However, no differences between the treated and untreated groups in the follicle density of primordial (1.69 ± 0.42 and 1.44 ± 0.47 follicles/mm2, respectively, with a total of 2349 follicles analysed, p = 0.33) and primary follicles (0.05 ± 0.02 and 0.05 ± 0.02 follicles/mm2, respectively, with a total of 65 follicles analysed, p = 0.32) (Figure 4B) or morphological anomalies of primordial (78.46 and 76.20% of morphologically normal follicles, respectively, respectively) and primary follicles (62.96 and 57.90% of morphologically normal follicles, respectively) (Figures 4C-D) were observed. In addition, the low density of secondary and more mature follicles prevented further statistical analysis.

Figure 4
figure 4

The analysis of fibrosis and follicles 3 weeks after transplantation. A. The percentage of fibrotic tissue in the ovarian transplant. B. Primordial and primary follicle quantification in H&E-stained sections (mean number/mm2). C. An illustration of primordial follicles that were considered to be morphologically normal (the plain arrow) or abnormal (the dotted arrow) with disorganised granulosa cells. D. The proportion of morphologically normal and abnormal primordial and primary follicles in the control group and the VEGF165-treated group. n corresponds to the number of ovarian fragments that were transplanted into mice. Scale bar: 200 μm. Error bar are SEM.

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Discussion

In this study, the effect of VEGF165 on slow-frozen, cryopreserved ewe ovarian tissue that was grafted into a murine model was analysed three days and three weeks after transplantation. The results of this study suggest that VEGF165 improves angiogenesis in ovarian grafts as soon as three days post-transplantation. In addition, this treatment enhanced vessel maturation because 50% of the ovarian transplants that were impregnated with VEGF165 exhibited mature vessels that were surrounded by alpha-smooth muscle cells. This rapid reconstruction of blood vessels in ovarian grafts is important for limiting ischemic injury, which has been demonstrated to induce the depletion of 60-95% of the follicular reserve, including the loss of virtually the entire population of growing follicles, during autograft processes [7,37-39]. This phenomenon has been associated with a dramatic reduction in graft size and significant fibrosis [40]. In this study, three weeks after transplantation, the extent of fibrosis was similar between the control and VEGF165-treated groups. We previously demonstrated that fibrosis that occurred three weeks after transplantation was partially due to the freeze-thawing procedure [8]. Therefore, more rapid revascularisation of the transplant after grafting due to the pro-angiogenic effect of VEGF165 was not likely to limit the development of fibrosis.

This study analysed ovarian fragments that were encapsulated in a collagen gel that contained VEGF165. Indeed, given the short half-life time of VEGF and in order to have a longer local delivery, a matrix containing VEGF was necessary. In our laboratory, encapsulation of ovarian fragment in a collagen gel had already been developed and proved efficacious. However, other teams have also study the release of VEGF in different models like alginate scaffold [41] or fibrin matrix [42-45]. In this study, the results regarding vascular improvement are in agreement with those from studies that used different systems, such as the encapsulation of ovarian fragments in a VEGF168 fibrin matrix and autologous murine transplantation [42-45]. Additionally, the combined effect of VEGF and basic fibroblast growth factor (bFGF) was found to increase graft survival in an experimental rabbit model of xenografted human ovarian tissue by triggering angiogenesis and by reducing apoptosis and fibrosis [45]. The present study confirmed that VEGF165 triggers the angiogenic process; however, VEGF165 did not reduce fibrosis or affect follicle survival.

The pre-existing vasculature can initiate the formation of new blood vessels either by sprouting, intussusception, or elongation via the incorporation of circulating endothelial cells [46]. In the context of the physiological angiogenic process of folliculogenesis, most of these processes are effective [47]. Ovarian tissue grafts are exposed to ischemic damage during the post-transplantation period until the vasculature develops. Vascular connections between the host and an ovarian strip that was grafted into a murine ovary were observed 5 days after transplantation [13]. To determine whether the addition of VEGF165 had a beneficial effect on vascular recruitment and limited the period of tissue hypoxia, transplanted fragments were analysed three days and three weeks after grafting. The analysis of vascularisation revealed that VEGF165 effectively improved graft vascularisation as early as three days post-transplantation. Moreover, a higher proportion of functional blood vessels (dextran FITC-positive vessels) and mature vessels (α-SMA) was observed. Using species-specific CD31 immunohistochemistry and double staining for functional and mature blood vessels (Dextran-FITC and α-SMA), we demonstrated the dual origin of angiogenesis (from the host and from the grafted tissue), as previously described [36]. Collectively, these data confirm the pro-angiogenic effect of VEGF165 and the presence of murine endothelial cell migration towards the sheep transplant. However, this improved vascularisation did not modulate the follicular density and did not alter the follicular morphology. In this study, follicular morphology was evaluated in several sections using light microscopy scoring as previously described [24]. VEGF165 was used in this study, following our encouraging results with VEGF111, because it offers the advantage, with respect to the 111 isoform, of existing both in free and matrix-bound forms, which could improve its release profile from the collagen matrix. However, in contrast to VEGF111, which has been demonstrated to preserve primary ovarian follicles and improve angiogenesis [23], VEGF165 failed to significantly decrease fibrosis or increase oocyte survival and morphology. Various VEGF isoforms have exhibited differences in mitogenicity, chemotactic efficacy, receptor interaction, and tissue distribution [48,49]. However, a direct comparison of VEGF111 and VEGF165 in terms of the follicular pool, survival, and morphology preservation has yet to be performed. Another key factor that affects the efficacy of cytokine treatments is the route of administration of these molecules. Skaznik-Wikiel et al. previously reported that intraperitoneal injections of VEGF164 for five days combined with subcutaneous injections of granulocyte colony-stimulating factor (G-CSF) maintained the primordial follicular pool [43]. In addition, Friedman et al. found that graft incubation with hyaluronan-rich biological glue combined with VEGF-A and vitamin E decreased the number of atretic follicles and the levels of apoptosis two weeks after grafting in a xenograft model [44]. Additionally, a recent study demonstrated that human ovarian graft incubation followed by hypodermic injections at the transplant site with a combination of VEGF and bFGF 7 days after transplantation improved angiogenesis and reduced apoptosis and fibrosis 6 weeks after transplantation [45]. Although these studies have demonstrated the beneficial effects of VEGF, they often used a method of systemic delivery of VEGF, which is not reasonable in the context of clinical usage in patients with cancer. The major advantage of our model was limiting local exposure to VEGF to the site of transplantation. Other molecules used without VEGF such as S1P [15], EPO [16], or PRP [17] have been shown to improve the quality of ovarian grafts and could therefore be interesting to study in combination with VEGF. Other molecules such as human menopausal gonadotropin (HMG) act indirectly, increasing endogenous VEGF secretion in a transplant after three hours of culture before grafting. HMG treatment accelerated revascularisation of the transplant and increased the number of surviving follicles one month after transplantation [50]. These data emphasise the potential benefits of combining different growth factors to prevent early ischemic damage, improve rapid revascularisation of the transplant, and maintain the follicular pool.

Conclusions

This study demonstrates that encapsulation of ovarian tissue with VEGF165 in a collagen matrix during xenografting in mice produces a more rapid onset of functional vessel formation and earlier revascularisation of the transplant. Collectively, our data suggest that the prevention of hypoxia during ovarian tissue grafting requires additional cofactors to preserve the follicular pool.