首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Molecular effect of human umbilical cord blood CD34-positive and CD34-negative stem cells and their conjugate in azoospermic mice
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Molecular effect of human umbilical cord blood CD34-positive and CD34-negative stem cells and their conjugate in azoospermic mice

机译:人脐血血液CD34阳性和CD34阴性干细胞及其在偶氮小鼠中的缀合物的分子效果

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Currently, azoospermia is one of the most common diseases of male infertility. Stem cell research is the new hope for novel therapy with a higher degree of safety and lower cost. This study aimed to investigate the effect of umbilical cord blood-derived stem cells (" and mesenchymal " UCB-MSCs") and mono-cell layer implanted into the induced azoospermic mice testis. Stem cells were isolated from umbilical cord blood and CD34+ ve cells were separated from negative one by Mini MACs column. At 5th week after single injection of busulfan, stained mesenchymal (CD34-ve), hematopoietic stem cells (CD34+ ve) and their conjugate (mono-cell layer) were injected locally into testis. At the end of the study, MSCs group showed that mRNA levels of genes related to meiosis (Vasa, SCP3, and PgK2) were increased with significant decrease of FSH and LH levels, compared to control group. Histologically, most of the tubules restored normal architecture. In contrast, HSCs and mono-cell layer groups showed statically insignificant change of FSH, LH, and gene expression, compared to control group. Histologically, distorted seminiferous tubules, with reduction in sperm content, and interstitial mononuclear cellular infiltration were seen. There was significant increase in the optical density of PCNA immune reaction in MSCs group than azoospermia, HSCs, and mono-cell layer, while there was non-significant difference between MSCs and control group. The present study suggested that injection of MSCs into chemotherapeutic- induced azoospermia in mice improved testicular failure; histologically and functionally, by restoration of spermatogenic gene expression while HSC and mono-cell layer showed no effect on spermatogenesis added to that mono-cell layer may induce testicular tissue damage.
机译:目前,Azoospermia是男性不孕症最常见的疾病之一。干细胞研究是新的疗法的新希望,具有较高的安全程度和更低的成本。本研究旨在探讨脐带血源性干细胞(“和间充质”UCB-MSCs“)和植入诱导的偶氮孢菌小鼠睾丸的单细胞层的影响。从脐带血和CD34 + VE细胞中分离干细胞用迷你MACS柱分离阴性1。在单一注射套簇的第5周,氨化间充质(CD34-VE),造血干细胞(CD34 + VE)及其缀合物(单细胞层)局部注射到睾丸中。在该研究结束,与对照组相比,MSCS组显示与减数分裂(VASA,SCP3和PGK2相关的基因MRNA水平随着FSH和LH水平的显着降低而增加。组织学上,大部分小管恢复了正常架构与对照组相比,HSC和单细胞层组显示出FSH,LH和基因表达的静态微不足道的变化。组织学上,扭曲的半成小管,并减少精子含量,和看到了不染句的单核细胞渗透。 MSCS组PCNA免疫反应的光密度显着增加,而不是唑孔果,HSC和单细胞层,而MSCs和对照组之间存在非显着差异。本研究表明,将MSC注入化学治疗诱导的小鼠中的抑制症改善睾丸衰竭;通过恢复精子源性基因表达的组织学和功能性,而HSC和单细胞层对添加到该单细胞层的精子发生没有影响,可以诱导睾丸组织损伤。

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