Department of Urology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
State Key Laboratory of Oncogenes and Related Genes, Renji-Med X Clinical Stem Cell Research Center, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
Stem Cell Res Ther. 2020 Jul 17;11(1):294. doi: 10.1186/s13287-020-01813-5.
This study was designed to determine the effect of human umbilical cord multipotent mesenchymal stromal cells (hUC-MSC) on acute ischemia/reperfusion (I/R) injury of spermatogenic cells.
The testicular I/R rat model was established through 720° torsion for 1 h. hUC-MSC were intravenously injected 10 min before detorsion. Injury severity of spermatogenic cells was estimated by Johnsen's score. The proliferating of recipient spermatogonia was measured by the immunostaining of antibodies against Ki67, and all germ cells were detected with DDX4 antibody. And recipient spermatogenesis was assessed by staining spermatozoa with lectin PNA. The levels of inflammatory factors were measured by real-time PCR. And the Selectin-E expression, neutrophil infiltration in the testes was detected by immunostaining. Germ cells apoptosis was tested by TUNEL assay and western blot. Furthermore, the oxidative stress was tested by reactive oxidative species (ROS) levels. In vitro, the condition medium (CM) of hUC-MSC was used to culture human umbilical vein endothelial cells (HUVECs), so as to assess the paracrine effect of hUC-MSC on HUVECs. The protein chip was used to measure the relative concentration of the secretory proteins in the CM of hUC-MSC.
hUC-MSC greatly alleviated the testicular injury induced by testis I/R. The levels of proinflammatory factors were downregulated by hUC-MSC in vivo and in vitro. Neutrophil infiltration, ROS, and germ cell apoptosis in testicular tissues were greatly reduced in the group of hUC-MSC. Paracrine factors secreted by hUC-MSC including growth factors, cytokines, and anti-inflammatory cytokine were rich.
This study demonstrated that intravenously injected hUC-MSC could protect the spermatogenic cells against I/R injury by reducing the inflammatory response, apoptosis, and acute oxidative injury. Paracrine mechanism of hUC-MSC may contribute to the protection of spermatogenic cells against I/R injury. Therefore, the present study provides a method for clinical treatment of attenuate I/R injury of spermatogenic cells.
本研究旨在探讨人脐带间充质干细胞(hUC-MSC)对生精细胞急性缺血/再灌注(I/R)损伤的影响。
通过 720°旋转 1 小时建立睾丸 I/R 大鼠模型。在扭转复位前 10 分钟静脉注射 hUC-MSC。通过约翰森评分评估生精细胞损伤程度。用 Ki67 抗体免疫染色检测受者精原细胞的增殖,用 DDX4 抗体检测所有生殖细胞。用 PNA 凝集素染色检测受者精子发生。实时 PCR 检测炎症因子水平。免疫组化检测选择素-E 表达和睾丸内中性粒细胞浸润。TUNEL 检测和 Western blot 检测生殖细胞凋亡。进一步通过活性氧(ROS)水平检测氧化应激。体外用人脐带静脉内皮细胞(HUVEC)培养 hUC-MSC 的条件培养基(CM),以评估 hUC-MSC 对 HUVEC 的旁分泌作用。用蛋白芯片检测 hUC-MSC CM 中分泌蛋白的相对浓度。
hUC-MSC 显著减轻睾丸 I/R 引起的睾丸损伤。hUC-MSC 在体内和体外均下调促炎因子水平。hUC-MSC 组睾丸组织中中性粒细胞浸润、ROS 和生殖细胞凋亡明显减少。hUC-MSC 分泌的旁分泌因子包括生长因子、细胞因子和抗炎细胞因子等。
本研究表明,静脉注射 hUC-MSC 可通过减轻炎症反应、凋亡和急性氧化损伤来保护生精细胞免受 I/R 损伤。hUC-MSC 的旁分泌机制可能有助于保护生精细胞免受 I/R 损伤。因此,本研究为临床治疗生精细胞 I/R 损伤提供了一种方法。