Department of Obstetrics and Gynecology, University of Chicago, Chicago, IL 60637, USA.
Department of Surgery, University of Chicago, Chicago, IL 60637, USA.
Int J Mol Sci. 2023 Dec 20;25(1):60. doi: 10.3390/ijms25010060.
Currently, there is no viable option for fertility preservation in prepubertal boys. Experimentally, controlled vitrification of testicular tissue has been evaluated and found to cause potential structural damage to the spermatogonial stem cell (SSC) niche during cryopreservation. In this report, we leveraged the regenerative effect of human umbilical cord-derived Mesenchymal stem cell exosomes (h-UCMSC-Exo) to protect against testicular damage from the cytotoxic effects of polychemotherapy (CTX). A chemotherapy-induced testicular dysfunctional model was established by CTX treatment with cyclophosphamide and Busulfan in vitro (human Sertoli cells) and in prepubescent mice. We assessed the effects of the exosomes by analyzing cell proliferation assays, molecular analysis, immunohistochemistry, body weight change, serum hormone levels, and fertility rate. Our data indicates the protective effect of h-UCMSC-Exo by preserving the SSC niche and preventing testicular damage in mice. Interestingly, mice that received multiple injections of h-UCMSC-Exo showed significantly higher fertility rates and serum testosterone levels ( < 0.01). Our study demonstrates that h-UCMSC-Exo can potentially be a novel fertility protection approach in prepubertal boys triaged for chemotherapy treatment.
目前,青春期前男孩的生育力保存尚无可行的选择。在实验中,已经评估了睾丸组织的控制性玻璃化冷冻,并发现冷冻保存过程中可能对精原干细胞(SSC)龛造成潜在的结构损伤。在本报告中,我们利用人脐带间充质干细胞外泌体(h-UCMSC-Exo)的再生作用来防止多化疗(CTX)的细胞毒性作用对睾丸造成损伤。通过体外(人支持细胞)和青春期前小鼠中用环磷酰胺和白消安进行 CTX 处理,建立了化疗诱导的睾丸功能障碍模型。我们通过分析细胞增殖试验、分子分析、免疫组织化学、体重变化、血清激素水平和生育力来评估外泌体的作用。我们的数据表明 h-UCMSC-Exo 通过保留 SSC 龛并防止小鼠睾丸损伤发挥保护作用。有趣的是,接受多次 h-UCMSC-Exo 注射的小鼠的生育力和血清睾酮水平明显更高(<0.01)。我们的研究表明,h-UCMSC-Exo 可能是一种新的生育力保护方法,可以用于接受化疗治疗的青春期前男孩。