EA 4308 "Gametogenesis and Gamete Quality", Reproductive Biology Laboratory - CECOS, Rouen University Hospital, Institute for Biomedical Research, University of Rouen, Rouen, France.
EA 4308 "Gametogenesis and Gamete Quality", Department of Urology, Rouen University Hospital, Institute for Biomedical Research, University of Rouen, Rouen, France.
PLoS One. 2013 Dec 9;8(12):e82819. doi: 10.1371/journal.pone.0082819. eCollection 2013.
Testicular tissue cryopreservation is the only potential option for fertility preservation in pre-pubertal boys exposed to gonadotoxic treatment. Completion of spermatogenesis after in vitro maturation is one of the future uses of harvested testicular tissue. The purpose of the current study was to evaluate the effects of vitamin A on in vitro maturation of fresh and frozen-thawed mouse pre-pubertal spermatogonial stem cells in an organ culture system. Pre-pubertal CD1 mouse fresh testes were cultured for 7 (D7), 9 (D9) and 11 (D11) days using an organ culture system. Basal medium was supplemented with different concentrations of retinol (Re) or retinoic acid (RA) alone or in combination. Seminiferous tubule morphology (tubule diameter, intra-tubular cell type), intra-tubular cell death and proliferation (PCNA antibody) and testosterone level were assessed at D7, D9 and D11. Pre-pubertal mouse testicular tissue were frozen after a soaking temperature performed at -7 °C, -8 °C or -9 °C and after thawing, were cultured for 9 days, using the culture medium preserving the best fresh tissue functionality. Retinoic acid at 10(-6)M and retinol at 3.3.10(-7)M, as well as retinol 10(-6)M are favourable for seminiferous tubule growth, maintenance of intra-tubular cell proliferation and germ cell differentiation of fresh pre-pubertal mouse spermatogonia. Structural and functional integrity of frozen-thawed testicular tissue appeared to be well-preserved after soaking temperature at -8 °C, after 9 days of organotypic culture using 10(-6)M retinol. RA and Re can control in vitro germ cell proliferation and differentiation. Re at a concentration of 10(-6)M maintains intra-tubular cell proliferation and the ability of spermatogonia to initiate spermatogenesis in fresh and frozen pre-pubertal mouse testicular tissue using a soaking temperature at -8 °C. Our data suggested a possible human application for in vitro maturation of cryopreserved pre-pubertal testicular tissue.
睾丸组织冷冻保存是暴露于性腺毒性治疗的青春期前男孩进行生育力保存的唯一潜在选择。体外成熟后完成精子发生是收获的睾丸组织的未来用途之一。本研究的目的是评估维生素 A 对新鲜和冷冻-解冻的青春期前小鼠精原干细胞在器官培养系统中的体外成熟的影响。使用器官培养系统培养青春期前 CD1 小鼠新鲜睾丸 7(D7)、9(D9)和 11(D11)天。基础培养基中单独或联合添加不同浓度的视黄醇(Re)或视黄酸(RA)。在 D7、D9 和 D11 时评估生精小管形态(小管直径、管内细胞类型)、管内细胞死亡和增殖(PCNA 抗体)以及睾酮水平。将青春期前小鼠睾丸组织在-7°C、-8°C 或-9°C 浸泡温度下冷冻,然后在解冻后使用保持最佳新鲜组织功能的培养基培养 9 天。10(-6)M 的视黄酸和 3.3.10(-7)M 的视黄醇以及 10(-6)M 的视黄醇有利于新鲜青春期前小鼠精原细胞的生精小管生长、管内细胞增殖和生殖细胞分化。在 -8°C 浸泡温度下,在使用 10(-6)M 视黄醇的 9 天器官型培养后,冷冻-解冻睾丸组织的结构和功能完整性似乎得到了很好的保存。RA 和 Re 可以控制体外生殖细胞增殖和分化。浓度为 10(-6)M 的 Re 维持管内细胞增殖和精原细胞在新鲜和冷冻青春期前小鼠睾丸组织中启动精子发生的能力,使用 -8°C 的浸泡温度。我们的数据表明,冷冻保存的青春期前睾丸组织的体外成熟可能具有潜在的人类应用。