The Shraga Segal Department of Microbiology, Immunology, and Genetics, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva 8410501, Israel.
The Center of Advanced Research and Education in Reproduction (CARER), Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva 8410501, Israel.
Int J Mol Sci. 2023 Jul 31;24(15):12229. doi: 10.3390/ijms241512229.
Pediatric acute myeloid leukemia (AML) generally occurs de novo. The treatment of AML includes cytarabine (CYT) and other medications. The granulocyte-colony stimulating factor (GCSF) is used in the clinic in cases of neutropenia after chemotherapies. We show that the administration of GCSF in combination with CYT in AML-diagnosed mice (AML+CYT+GCSF) extended the survival of mice for additional 20 days. However, including GCSF in all treatment modalities does not affect the testis' weight or the histology of the seminiferous tubules (STs). We show that GCSF does not affect normal ST histology from AML-, CYT-, or (AML+CYT)-treated groups compared to the relevant treated group without GCSF 2, 4, and 5 weeks post-injection. However, when comparing the percentages of normal STs between the AML+CYT+GCSF-treated groups and those without GCSF, we observe an increase of 17%-42% in STs at 4 weeks and 5.5 weeks post-injection. Additionally, we show that the injection of GCSF into the normal, AML-alone, or CYT-alone groups, or in combination with AML, significantly decreases the percentage of STs with apoptotic cells compared to the relevant groups without GCSF and to the CT (untreated mice) only 2 weeks post-injection. We also show that injection of GCSF into the CT group increases the examined spermatogonial marker PLZF within 2 weeks post-injection. However, GCSF does not affect the count of meiotic cells (CREM) but decreases the post-meiotic cells (ACROSIN) within 4 weeks post-injection. Furthermore, GCSF not only extends the survival of the AML+CYT-treated group, but it also leads to the generation of sperm (1.2 ± 0.04 × 10/mL) at 5.5 weeks post-injection. In addition, we demonstrate that the injection of GCSF into the CT group increases the RNA expression level of IL-10 but not IL-6 compared to CT 2 weeks post-treatment. However, the injection of GCSF into the AML-treated group reverses the expression levels of both IL-10 and IL-6 to normal levels compared to CT 2 weeks post-injection. Thus, we suggest that the addition of GCSF to the regimen of AML after CYT may assist in the development of future therapeutic strategies to preserve male fertility in AML prepubertal patients.
儿科急性髓系白血病(AML)通常是新发的。AML 的治疗包括阿糖胞苷(CYT)和其他药物。粒细胞集落刺激因子(GCSF)在化疗后中性粒细胞减少症的情况下在临床上使用。我们发现,在 AML 诊断的小鼠中(AML+CYT+GCSF)联合 GCSF 和 CYT 给药可将小鼠的存活时间延长 20 天。然而,在所有治疗方式中包括 GCSF 并不影响睾丸的重量或生精小管(STs)的组织学。我们发现,与未接受 GCSF 的相关治疗组相比,在 AML、CYT 或(AML+CYT)治疗组中,GCSF 不影响正常 ST 组织学,在注射后 2、4 和 5 周时均如此。然而,当比较 AML+CYT+GCSF 治疗组与未接受 GCSF 的组之间正常 ST 的百分比时,我们观察到在注射后 4 周和 5.5 周时,ST 的比例增加了 17%-42%。此外,我们发现,与未接受 GCSF 的组和 CT(未治疗的小鼠)相比,将 GCSF 注射到正常、AML 单独或 CYT 单独的组中,或与 AML 联合注射,显著降低了具有凋亡细胞的 ST 百分比,仅在注射后 2 周。我们还发现,将 GCSF 注射到 CT 组中,可在注射后 2 周内增加所检查的精原细胞标志物 PLZF。然而,GCSF 不影响减数分裂细胞(CREM)的计数,但在注射后 4 周内降低了减数分裂后细胞(ACROSIN)的数量。此外,GCSF 不仅延长了 AML+CYT 治疗组的存活时间,而且还导致在注射后 5.5 周时产生精子(1.2±0.04×10/mL)。此外,我们证明,与 CT 相比,在注射后 2 周内,将 GCSF 注射到 CT 组中可增加 IL-10 的 RNA 表达水平,但不增加 IL-6。然而,与 CT 相比,在注射后 2 周内,将 GCSF 注射到 AML 治疗组中可使 IL-10 和 IL-6 的表达水平恢复正常。因此,我们建议在 AML 后 CYT 治疗方案中添加 GCSF,以协助制定未来的治疗策略,以维持 AML 青春期前患者的男性生育能力。