Sonia Herraiz1, Edurne Novella-Maestre2, Beatriz Rodríguez3, César Díaz3, María Sánchez-Serrano4, Vicente Mirabet5, Antonio Pellicer3. 1. Grupo de Investigación de Medicina Reproductiva, Instituto de Investigación Sanitario La Fe, Valencia, Spain; Unidad de Preservación de la Fertilidad, Área de Salud de la Mujer, Hospital Universitario y Politécnico La Fe, Valencia, Spain. 2. Grupo de Investigación de Medicina Reproductiva, Instituto de Investigación Sanitario La Fe, Valencia, Spain; Unidad de Preservación de la Fertilidad, Área de Salud de la Mujer, Hospital Universitario y Politécnico La Fe, Valencia, Spain; Unidad de Genética, Hospital Universitario y Politécnico La Fe, Valencia, Spain. Electronic address: edurnenovella@yahoo.es. 3. Grupo de Investigación de Medicina Reproductiva, Instituto de Investigación Sanitario La Fe, Valencia, Spain; Unidad de Preservación de la Fertilidad, Área de Salud de la Mujer, Hospital Universitario y Politécnico La Fe, Valencia, Spain; Departamento de Pediatría, Obstetricia y Ginecología, Facultad de Medicina, Universidad de Valencia, Valencia, Spain. 4. Departamento de Obstetricia y Ginecología, Hospital Clínico Universitario, Valencia, Spain. 5. Banco de Tejidos, Centro de Transfusión de la Comunidad Valenciana, Valencia, Spain.
Abstract
OBJECTIVE: To compare slow freezing (SF) with four vitrification techniques (VT) for cryopreservation of ovarian tissue (OT) and to evaluate the best protocol for human OT in a xenograft model. DESIGN: Experimental study. SETTING: University hospital. PATIENT(S): Patients undergoing fertility preservation. ANIMAL(S): Ovariectomized nude mice. INTERVENTION(S): Cryopreservation of bovine OT after SF and four VTs (VT1, VT2, VT3, and VT4) by combining two cryoprotectant vitrification solutions (VS1 and VS2) and two devices (metallic grid and ethyl vinyl acetate bag), after which the cryopreservation of human OT by SF and VT1 and xenograft into nude mice. MAIN OUTCOME MEASURE(S): Follicular densities, proliferation, vascularization, fibrosis, apoptosis, tissue viability. RESULT(S): The in vitro study in bovine OT showed a lower percentage of quiescent follicles in the SF group but not in the vitrification groups (VT1-VT4). Apoptosis increased and cell proliferation decreased in all the experimental groups except VT1 (20% ethylene glycol, 20% dimethyl sulfoxide, 0.5 M sucrose, and 20% synthetic serum substitute in HEPES-buffered M199 culture media with Cryotissue metallic grids). Tissue viability was diminished in VT3, and the SF-xenografted human samples showed reduced primordial and secondary densities and unbalanced follicular populations when compared with fresh and VT1 tissue. CONCLUSION(S): VT1 offers similar conditions to fresh tissue for follicular density, proliferation, viability, and cell death and preserves a larger population of quiescent follicles than SF after transplantation, thus ensuring the maintenance of graft potential fertility.
OBJECTIVE: To compare slow freezing (SF) with four vitrification techniques (VT) for cryopreservation of ovarian tissue (OT) and to evaluate the best protocol for human OT in a xenograft model. DESIGN: Experimental study. SETTING: University hospital. PATIENT(S): Patients undergoing fertility preservation. ANIMAL(S): Ovariectomized nude mice. INTERVENTION(S): Cryopreservation of bovine OT after SF and four VTs (VT1, VT2, VT3, and VT4) by combining two cryoprotectant vitrification solutions (VS1 and VS2) and two devices (metallic grid and ethyl vinyl acetate bag), after which the cryopreservation of human OT by SF and VT1 and xenograft into nude mice. MAIN OUTCOME MEASURE(S): Follicular densities, proliferation, vascularization, fibrosis, apoptosis, tissue viability. RESULT(S): The in vitro study in bovine OT showed a lower percentage of quiescent follicles in the SF group but not in the vitrification groups (VT1-VT4). Apoptosis increased and cell proliferation decreased in all the experimental groups except VT1 (20% ethylene glycol, 20% dimethyl sulfoxide, 0.5 M sucrose, and 20% synthetic serum substitute in HEPES-buffered M199 culture media with Cryotissue metallic grids). Tissue viability was diminished in VT3, and the SF-xenografted human samples showed reduced primordial and secondary densities and unbalanced follicular populations when compared with fresh and VT1 tissue. CONCLUSION(S): VT1 offers similar conditions to fresh tissue for follicular density, proliferation, viability, and cell death and preserves a larger population of quiescent follicles than SF after transplantation, thus ensuring the maintenance of graft potential fertility.
Authors: M M Dolmans; M M Binda; S Jacobs; J P Dehoux; J L Squifflet; J Ambroise; J Donnez; C A Amorim Journal: J Assist Reprod Genet Date: 2015-08-04 Impact factor: 3.412