MRC Centre for Reproductive Health, The Queen's Medical Research Institute, The University of Edinburgh, 47 Little France Crescent, Edinburgh, EH16 4TJ, Scotland, UK.
State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, China.
BMC Cancer. 2023 Mar 16;23(1):251. doi: 10.1186/s12885-023-10702-y.
Currently there are no established fertility preservation options for pre-pubertal boys facing cancer treatment. Granulocyte-colony stimulating factor (G-CSF) treatment has been proposed to be chemoprotective against spermatogonial cell loss in an alkylating chemotherapy model of busulfan treated adult mice. Having previously shown that exposure to the alkylating-like chemotherapy cisplatin resulted in a reduction in germ cell numbers in immature human testicular tissues, we here investigate whether G-CSF would prevent cisplatin-induced germ cell loss in immature human and mouse (fetal and pre-pubertal) testicular tissues.
Organotypic in vitro culture systems were utilised to determine the effects of clinically-relevant concentrations of G-CSF in cisplatin-exposed immature testicular tissues. Human fetal (n = 14 fetuses) and mouse pre-pubertal (n = 4 litters) testicular tissue pieces were cultured and exposed to cisplatin or vehicle control for 24 hrs and analysed at 72 and 240 hrs post-exposure. Combined G-CSF and cisplatin exposure groups explored varying concentrations and duration of G-CSF supplementation to the culture medium (including groups receiving G-CSF before, during and after cisplatin exposure). In addition, effects of G-CSF supplementation alone were investigated. Survival of total germ cell and sub-populations were identified by expression of AP2γ and MAGE-A4 for human gonocytes and (pre)spermatogonia, respectively, and MVH and PLZF, for mouse germ cells and putative spermatogonial stem cells (SSCs) respectively, were quantified.
Exposure to cisplatin resulted in a reduced germ cell number in human fetal and mouse pre-pubertal testicular tissues at 240 hrs post-exposure. Germ cell number was not preserved by combined exposure with G-CSF using any of the exposure regimens (prior to, during or after cisplatin exposure). Continuous supplementation with G-CSF alone for 14 days did not change the germ cell composition in either human or mouse immature testicular tissues.
This study demonstrates that exposure to G-CSF does not prevent cisplatin-induced germ cell loss in immature human and mouse testicular tissues in an in vitro system.
目前,对于面临癌症治疗的青春期前男孩,尚无既定的生育力保存选择。粒细胞集落刺激因子(G-CSF)治疗已被提议在烷化剂化疗模型中对接受白消安治疗的成年小鼠的精原细胞损失具有化学保护作用。先前我们已经表明,暴露于烷化剂样化疗药物顺铂会导致未成熟人类睾丸组织中的生殖细胞数量减少,因此我们在此研究 G-CSF 是否会阻止未成熟人类和小鼠(胎儿和青春期前)睾丸组织中的顺铂诱导的生殖细胞损失。
利用器官型体外培养系统来确定临床上相关浓度的 G-CSF 在暴露于顺铂的未成熟睾丸组织中的作用。人类胎儿(n=14 例胎儿)和小鼠青春期前(n=4 窝)睾丸组织块进行培养,并暴露于顺铂或载体对照 24 小时,然后在暴露后 72 和 240 小时进行分析。联合 G-CSF 和顺铂暴露组探索了向培养基中添加 G-CSF 的不同浓度和持续时间(包括在顺铂暴露前、期间和之后接受 G-CSF 的组)。此外,还研究了单独添加 G-CSF 的影响。通过表达 AP2γ 和 MAGE-A4 鉴定人类生殖细胞和(前)精原细胞的总生殖细胞和亚群的存活,通过 MVH 和 PLZF 鉴定小鼠生殖细胞和假定的精原干细胞(SSC)的存活。
在暴露后 240 小时,顺铂暴露导致人类胎儿和小鼠青春期前睾丸组织中的生殖细胞数量减少。使用任何暴露方案(在顺铂暴露之前、期间或之后),联合使用 G-CSF 均不能保留生殖细胞数量。连续单独补充 G-CSF 14 天不会改变人类或小鼠未成熟睾丸组织中的生殖细胞组成。
本研究表明,在体外系统中,G-CSF 的暴露并不能防止未成熟的人类和小鼠睾丸组织中的顺铂诱导的生殖细胞损失。