不同注射方式骨髓间充质干细胞移植治疗buslfan诱导雄性大鼠不育症的潜力。

IF 1.1 Q4 CELL & TISSUE ENGINEERING
Journal of Stem Cells & Regenerative Medicine Pub Date : 2024-10-13 eCollection Date: 2024-01-01 DOI:10.46582/jsrm.2002005
Samar Abdelbaset, Mohamed Ahmed Mohamed Sob, Ghada Mutawa, Mai Alaa El-Dein, Amoura Mohamed Abou-El-Naga
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引用次数: 0

摘要

背景:近年来,骨髓间充质干细胞(BM-derived MSCs)已成为一种强大的基于细胞的治疗多种疾病的方法,包括男性不育。目的:探讨不同注射途径对脑源性骨髓间充质干细胞移植修复布苏芬诱导的无精子大鼠睾丸的效果。材料和方法:本研究分离了大鼠脑源性间充质干细胞,并用流式细胞术对其间充质和造血标志物进行了表征。用连续两次剂量的10 mg/kg丁硫丹诱导不孕症。无精子大鼠通过多种途径(IP、IV和睾丸局部)注射脑脊髓瘤来源的间充质干细胞。60天后;精子分析主要进行生化、组织病理学、免疫组织学和超微结构检查。结果:bm来源的MSCs分别表达CD44+ve、CD105+ve、CD106+ve、CD73+ve、CD34-ve和CD45-ve。精子分析显示,用脑卒中来源的间充质干细胞治疗后,精子形态、活力和数量有了实质性的改善。Caspase-3和PCNA的免疫表达以及FSH、LH、睾酮、SOD、GSH和MDA的水平表明,在脑转移的MSCs治疗后,健康水平得到了相当大的恢复。对脑源性间充质干细胞处理后的大鼠进行组织病理学和超微结构分析,发现精小管形态健康,管腔内可见精子。有趣的是,静脉注射脑内来源的间充质干细胞显示出最显著的不育修复结果(结论:移植的脑内来源的间充质干细胞有可能在无精子的大鼠睾丸中归家并恢复精子发生。因此,bm来源的MSCs的独特特征,如它们的分化和分化能力,使它们成为男性不育症的一个有希望的基于细胞的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic Potential of Different Injection Methods for Bone Marrow Mesenchymal Stem Cell Transplantation in Buslfan-Induced Male Rat Infertility.

Background: In recent years, bone marrow derived mesenchymal stem cells (BM-derived MSCs) have emerged as a powerful cell-based therapy for various diseases, including male infertility. Aim: Demonstrating the efficiency of BM-derived MSCs transplantation by different routes of injection to home and repair testis of busulfan-induced azoospermic rats. Material and methods: In the present study, rat BM-derived MSC was isolated and characterized for mesenchymal &hematopoietic markers using flow-cytometry. Induction of infertility was induced by two successive doses of 10 mg/kg of busulfan. Azoospermic rats were treated by BM-derived MSCs which were injected via various routes (IP, IV, and local in testis). After 60 days; sperm analyses were performed beside mainly Biochemical, histopathological, immunohistological, and ultrastructural investigations. Results: BM-derived MSCs were expressed by CD44+ve, CD105+ve, CD106+ve, CD73+ve, CD34-ve, and CD45-ve. Sperm analysis showed a substantial improvement in sperm morphology, motility, and count following treatment with BM-derived MSCs. Caspase-3 and PCNA immunoexp ression accompanied with the levels of FSH, LH, testosterone, SOD, GSH and MDA depicted a considerable restoration of healthy levels after BM-derived MSCs treatment. The seminiferous tubules showed healthy morphology and spermatozoa were detected in their lumen according to the histopathological and ultrastructural analysis of BM-derived MSCs treated rats. Interestingly, BM-derived MSCs intravenous injection revealed the most significant infertility repair outcomes (P<0.05). Conclusion: Transplanted BM-derived MSCs had the potential to home in rat azoospermic testes and restore spermatogenesis. Consequently, the distinctive characteristics of BM-derived MSCs, such as their ability to differentiate and home, make them a promising cell-based therapeutic option for male infertility.

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